The gene family of human kallikrein-related peptidases (KLKs) encodes proteins with diverse and pleiotropic functions in normal physiology as well as in disease states. Currently, the most widely known KLK is KLK3 or prostate-specific antigen (PSA) that has applications in clinical diagnosis and monitoring of prostate cancer. The KLK gene family encompasses the largest contiguous cluster of serine proteases in humans which is not interrupted by non-KLK genes. This exceptional and unique characteristic of KLKs makes them ideal for evolutionary studies aiming to infer the direction and timing of gene duplication events. Previous studies on the evolution of KLKs were restricted to mammals and the emergence of KLKs was suggested about 150 million years ago (mya). In order to elucidate the evolutionary history of KLKs, we performed comprehensive phylogenetic analyses of KLK homologous proteins in multiple genomes including those that have been completed recently. Interestingly, we were able to identify novel reptilian, avian and amphibian KLK members which allowed us to trace the emergence of KLKs 330 mya. We suggest that a series of duplication and mutation events gave rise to the KLK gene family. The prominent feature of the KLK family is that it consists of tandemly and uninterruptedly arrayed genes in all species under investigation. The chromosomal co-localization in a single cluster distinguishes KLKs from trypsin and other trypsin-like proteases which are spread in different genetic loci. All the defining features of the KLKs were further found to be conserved in the novel KLK protein sequences. The study of this unique family will further assist in selecting new model organisms for functional studies of proteolytic pathways involving KLKs.
Citation: Pavlopoulou A, Pampalakis G, Michalopoulos I, Sotiropoulou G (2010) Evolutionary History of Tissue Kallikreins. PLoS ONE 5(11): e13781. doi:10.1371/journal.pone.0013781
Editor: Robert DeSalle, American Museum of Natural History, United States of America
Received: July 2, 2010; Accepted: October 8, 2010; Published: November 1, 2010
Copyright: © 2010 Pavlopoulou et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors acknowledge financial support by K. Karatheodoris grant (C.186) funded by the Research Committee (ELKE) of the University of Patras (http://www.upatras.gr/index/page/id/70/lang/en). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Human tissue kallikrein-related serine peptidases (KLKs) constitute a single family of 15 highly conserved trypsin- or chymotrypsin-like serine proteases encoded by the largest contiguous cluster of protease-encoding genes (KLK1-15) in the human genome mapped to chromosomal locus 19q13.4 . The most widely known member of the KLK family is KLK3 or PSA (prostate-specific antigen) that has applications in the diagnosis and monitoring of prostate cancer . The KLK contiguous cluster is not interrupted by other non-KLK genes, an additional feature that makes this family unique. Collectively, all the above characteristics establish the KLK family as a family of great importance for evolutionary studies. Tissue KLKs are usually divided into two groups the “classical” and the “non-classical” KLKs. The term “classical” KLKs is referred to the first members of the human KLK family that were identified, namely KLK1, KLK2, and KLK3 (PSA), whereas the rest are often referred to as “non-classical” , .
All currently reported KLK genes encode for single-chain prepro-enzymes with lengths varying between 244 and 293 amino acid residues and approximately share 40% protein identity. The preproKLKs are proteolytically processed to enzymatically inactive proKLKs that are secreted via the removal of an amino-terminal signal peptide. Subsequently, proKLKs are activated to mature peptidases extracellularly by specific proteolytic cleavage of their amino-terminal propeptide, a key step in the regulation of KLK function , –. Characteristic features of KLKs are the invariant residues of the active-site catalytic triad His57, Asp102 and Ser195, as well as a conserved Gly193 (human chymotrypsin numbering system) which is implicated in stabilizing the oxyanion intermediate of the internal peptide bond during hydrolysis .
KLKs are expressed in a wide variety of tissues including the pancreas, heart, lung, central nervous system, salivary glands and endocrine-regulated tissues such as thyroid, breast, testis, ovary, prostate, indicating that they participate in important biological processes , . Indeed, several lines of evidence support that KLKs cooperate in complex proteolytic cascade pathways to regulate physiological and pathological processes , . For instance, KLK5, KLK7 and KLK14 are involved in skin desquamation and other skin diseases – while KLK2, KLK3 and KLK5 have been involved in seminal plasma liquefaction , . Of particular note, KLKs are implicated in different stages of cancer development and progression and have emerged as powerful tumor markers as demonstrated by the PSA testing .
Previous efforts focused on the evolutionary history of KLKs focused in the characterization of the mouse , , rat ,  and pig genes , as well as of individual members in mastomys , cynomolgus monkey , rhesus monkey , , dog , guinea pig , macaque orangutan, chimpanzee, gorilla , cat , horse and cow ,  and cotton-top tamarin . Elliot et al.  had performed the first Bayesian phylogenetic analysis and suggested the origin of the KLK family before the marsupial-placental split (approximately 125–175 million years ago, mya). An additional advantage in evolution studies has emerged based on the huge number of sequences deposited in the public databases and the availability of an increasing number of sequenced genomes, as well as the availability of computational tools for crossgenome analyses.
In the present study, a comprehensive phylogenetic analysis of the KLK proteins was performed employing a maximum likelihood-based method in order to unravel the evolutionary history of the KLK family. Interestingly, three reptilian, two avian and one amphibian KLK homologues were detected which allowed us to trace the evolutionary origin of KLKs earlier than it was previously thought, approximately 330 mya. Primary sequences, as well as the predicted secondary and tertiary structures of putative KLK peptide sequences were analyzed. The genomic organization of the KLK genes was further examined and it was shown that in different species these genes cluster together at syntenic loci. Collectively, we suggest that KLKs are also present in non-therian species covering an evolutionary distance from amphibia to eutheria and they cluster at a single locus.
Identification of KLK homologous proteins
The complete or almost complete genomes of species representing major taxonomic divisions (according to the NCBI taxonomy database)  were searched for putative KLK protein sequences. Collectively, 260 KLK homologous protein sequences were identified in 26 species, as follows: primates (78), rodentia (57), carnivore (24), insectivore (9), perissodactyla (12), cetartiodactyla (23), chiroptera (12), afrotheria (15), xenarthra (5), metatheria (14), prototheria (5), sauria (3), aves (2), amphibia (1), pisces (0), ascidia (0) and insect (0).
All identified sequences are depicted in Table S1. As shown in Figure 1, the amino acid residues corresponding to the active site residues (chymotrypsin numbering: His57, Asp102 and Ser195) are conserved among species. The core trypsin domain of the 260 retrieved sequences was used to reconstruct a maximum likelihood-based phylogenetic tree (Figure 2). The recently released zebrafinch and platypus genomes ,  allowed us also to identify novel partial KLK-like sequences (zebra finch) (Table S1) which were not included in the phylogenetic analysis because they would decrease the resolution of the phylogenetic tree. In this tree, 13 coherent monophyletic branches were identified which permitted the preliminary classification of the candidate KLK protein sequences into 13 groups (Figure 2). Subsequently, a sample of 87 KLK protein sequences was chosen for more accurate phylogenetic analysis using the maximum likelihood method (Figure 3). This selection was done based on representative taxa (from the main taxonomic divisions). The generated tree is overall well-supported (Figure 3). The low bootstrap values in some deep-branching nodes suggest alternative branching. In the inferred phylogenetic tree, 13 highly resolved clades are distinguished which correspond to the classical KLKs (KLK1 to KLK3) and the other 12 KLK members (KLK4 to KLK15) (Figure 3). Interestingly, three reptilian KLK-related sequences appear to form their own separate clades, with relatively high support values, and they were arbitrarily referred to as “orphan KLKs” (Figures 2 and 3). Importantly, examination of the chromosomal localization of the KLK genes in different species reveals that the position and orientation of these genes are highly preserved (Figure 4). In addition, as is demonstrated in Figure S1 the splicing patterns are consistent between all KLK sequences, and the amino acid residues encompassing the active site are located in different exons as in human KLK genes.
The number of each of the motifs is indicated below. The height of each letter is proportional to the frequency of the corresponding residue at that position, and the letters are ordered so the most frequent is on top. The conserved catalytic triad residues are indicated with asterisks. The dot indicates the conserved glycine residue present in the oxyanion hole.
The support values (>50%) are indicated at the nodes. The branch lengths depict evolutionary distance. The trypsin proteins are used as outgroup. The scale bar at the upper right denotes evolutionary distance of 0.1 amino acids per position.
Bootstrap values (>50%) are indicated at the nodes. The branch lengths depict evolutionary distance. The trypsin proteins are used as outgroup. The scale bar at the upper right denotes evolutionary distance of 0.2 amino acids per position.
The orientation and approximate position and size of the kallikrein genes. The KLK encoding genes are shown as filled arrowheads, whereas the KLK pseudogenes are represented by open arrowheads. The KLK2, KLK2-ps and KLK3 genes are indicated by red. Loci are drawn in approximate scale. On the left, a NCBI taxonomy-based cladogram shows the evolutionary relationships of taxa and the taxonomic classes.
Conservation of KLK defining structural features in KLK homologous proteins
As mentioned previously, the identified KLK homologues contain the invariant residues of the active-site catalytic triad (Figure 1). However, the conserved glycine residue of motif 3 which is highly conserved in serine proteases is not conserved in KLK10 orthologues. This discrepancy is due to the fact that the KLK10 homologues contain a Gly193Ser substitution . Platypus is an exception however, being the only animal found to have conserved Gly193 in KLK10, probably indicating that this mutation was later introduced in order for the protein to acquire a very strict specificity and likely a highly specific biological function. Interestingly, a recent study failed to demonstrate enzymatic activity for KLK10 against synthetic substrates, suggesting that either KLK10 is inactive or it is highly specific for a single substrate, yet to be identified . Mouse KLK13 points to the later direction since, although it has the Gly193Asp mutation, it possesses enzymatic activity . Another exception is the presence of mutation at Asp102Ala (chymotrypsin numbering) in KLK2 of Rhesus monkey (Macaca mulata). This mutation renders the enzyme inactive, since Asp102 is a catalytic residue.
Furthermore, it is demonstrated that the novel KLK amino acid sequences possess the secondary structure of known KLKs – (Figure 5a). The degree of conservation of the four catalytically important amino acids is shown in the known three dimensional structure of human proKLK6  (Figure 5b) where they appear to be located in the most conserved region which is the cleft between the two trypsin-like serine protease domains (thrombin, subunit H beta-barrels; CATH Code: 22.214.171.124).
Sequences corresponding to the conserved trypsin domain were aligned using PROMALS3D. The residues of the catalytic triad are shown on the black background; the glycine residue is shown on the gray background. The consensus secondary structure is shown at the bottom, where the α-helices are represented by cylinders and the β-sheets by arrows. KLKs with known crystal structure were used as reference; their PDB accession codes are: KLK1(1spj), KLK5(2psy), KLK6 (1gvl). B, Tertiary structure of proKLK6. Graphic visualization of the human proKLK6 protein color coded by conservation score, where the region in blue corresponds to the most highly conserved region. KLK6 is represented as a cartoon. The four conserved amino acid residues (His 57, Asp102, Ser195 and Gly193) are indicated.
Organization of the KLK cluster
The exponential accumulation of genomic sequences allowed us to study the evolution of the KLK gene family in different species. As shown in Figure 4 and mentioned previously, the putative KLK proteases are encoded by uninterrupted, contiguous clusters of genes-at least in the most complete genomes - suggesting a preserved standard sequential order. This co-clustering of KLKs at a single locus is opposed to the other multigene peptide families where the paralogous genes are scattered on a one or multiple chromosomes . However, due to incomplete genomic studies, KLK genes of several species  are ‘dispersed’ in different genomic scaffolds (Figure 4). For this reason, a KLK member is considered to be absent only if the gene is not detected and at the same time the KLK genes that flank it in the prototypical sequential order (1) are detected in the same chromosome/scaffold/contig. The two KLK2 pseudogenes (KLK2-ps) found in murinae  were included in the analysis in order to enhance our understanding regarding the evolution of the KLK2 gene.
Phylogenetic analyses of the KLK family
The two phylogenetic trees (Figures 2 and 3), reconstructed using the maximum likelihood method, are congruent with similar topologies. These phylogenies suggest that, apart from the fifteen “conventional” KLK family members, three ‘orphan’ KLKs are present in anole lizard. The lizard KLK orphans appear to arise from the basal node (Figure 4) leading to the suggestion that they are the members of the KLK family that diverged earliest (“proto-KLKs”). There are three lines of evidence which suggest that these are true KLKs: (a) true KLK hits were yielded in a reciprocal BLAST, (b) a lizard trypsin exists which clusters with the fellow trypsins (Figure 3), (c) the lizard KLK genes are arranged in tandem repeats in a single genomic scaffold (Figure 4). KLK6, KLK14 and KLK15 were detected for first time in Prototheria (Figure 4). Besides, KLK15 is present in all organisms from Prototheria up to humans (Figure 4). KLK7, KLK8 and KLK13 apparently arrived later in the KLK family since they were both detected first in metatheria (Figure 4). Regarding KLK1, it was first detected in amphibia as a bona fide KLK and then appeared again in afrotheria whereas KLK2 was detected in laurasiatheria for the first time (Figure 4). We propose that the KLK2 gene is the result of the duplication/inversion of the KLK1 gene in an early laurasiatherian mammal. The findings above are in agreement with a previously proposed hypothesis ,  for eutherian evolution. According to this hypothesis xenarthra and afrotheria are sister groups -with xenarthra being the more ancient- placed at a basal position relative to the laurasiatheria and euarchontoglires. The presence of KLK2 in carnivora, insectivora and perissodactyla and its absence in cetartiodactyla and chiroptera (Figure 4) triggers that speculation that a KLK2 gene may have existed in these species which was either deleted or arose later in laurasiatherian evolution. In such an event the KLK2 gene was inactivated later in the course of evolution in the murine lineage resulting to a KLK2 pseudogene (Figure 4). Also, in gorilla, the KLK2 gene must have been deleted in the course of evolution, since it has been reported to have only exons I and V and we were also unable to identify the gene . Instead, several duplications of the KLK1 gene occurred later in the evolution yielding 13 KLK1 homologues in the mouse genome and 9 KLK1 homologues in the rat genome (Figure 4). Both the inactivation of KLK2 and the series of KLK1 duplication events apparently occurred after the divergence of the murine from other rodents such as the kangaroo rat since a functional KLK2 exists and no duplication of KLK1 was observed in its genome.
The KLK2 gene maintains the same orientation in all genomes except in perissodactyla suggesting that the direction of KLK2 transcription differs from species to species. Although, the equine KLK2 has a predicted chymotrypsin-like specificity similar to that of KLK3 , it shares the highest degree of sequence identity with KLK2 (data not shown), thus the symbol KLK2 was assigned to this protein. The canine KLK2 enzyme, though, was found to display proteolytic specificity similar to that of KLK2 but not KLK3 . We propose a duplication event of KLK2 which produced a KLK3 in catarrhini. Both KLK2 and KLK3 enzymes are secreted by the prostate gland where the zymogen KLK3 was shown to be activated by KLK2 . The presence of these two enzymes in humans, apes and Old World monkeys (Figure 4) leads to the suggestion that these enzymes are involved in physiological processes that are specific to catarrhini primates as outlined later. The classical KLKs form their own separate clade that is highly supported (Figure 2 and 3). The monophyletic groups KLK9 and KLK11 appear to have strong homology as confirmed by relatively high bootstrap values (Figures 2 and 3), triggering the speculation that tandem duplication events, apparently before the marsupial-placental divergence, may have copied KLK9 and KLK11. Similarly, KLK4 appears to be the product of a KLK5 duplication which has occurred presumably after the marsupial-placental split (Figures 2 and 3). On the other hand, KLK10 and KLK12 appear to be sister groups (Figures 2 and 3), suggesting another duplication event. Since the Gly193Ser substitution is specific to KLK10 members (with the exception of platypus) it would be reasonable to suggest that this substitution took place after the KLK10/KLK12 duplication. Interestingly, the branches of the KLK10 clade are exceptionally long, suggesting that the KLK10 members evolved more rapidly compared to the other KLKs.
The identification of an amphibian KLK1 permits to trace the evolutionary origin of KLKs 330 mya, when amphibia emerged . However, our phylogenetic analysis showed that no proto-KLKs are present in the frog (Figures 2 and 3). One plausible explanation is that the ancestor of the reptilian orphan KLKs, a trypsin-like proto-orphan KLK emerged in amphibia; a series of gene duplication and deletion events gave rise to KLK1-KLK15 that can be found in the contemporary genomes.
The reconstructed phylogenetic tree in Figure S2 also demonstrates that the two piscine peptide sequences previously described as KLK-related  are totally unrelated to KLKs. Instead these proteins cluster with the known complement factor D/adipsin proteins ,  (Figure S2). Finally, Figure 6 summarizes the evolution events in the KLK gene family.
Schematic representation of key events occurring through the evolutionary history of KLKs.
Rate shift analysis
Rate shift analyses were carried out as described . They were used to analyze the frog KLK and the subfamilies of KLK7, KLK10 and KLK2. Regarding the frog KLK, as shown in Figure 7 the most significant rate shifts occur between the frog KLK1 and the three orphan lizard KLKs (9 positions with significant rate shifts) rather between the frog and the other KLK1 proteins, where 4 positions with significant rate differences were found. These results support the phylogenetic analysis which suggests that the frog KLK is phylogenetically closer to the KLK1 proteins than to the lizard KLKs. For the KLK7, KLK10 and KLK12 it was found that lower rate shifts (12 positions) existed between KLK10 and KLK12 compared to KLK7 and KLK12 (16 positions) and KLK7 and KLK10 (26 positions) (Figure S3) which is also in accordance with the phylogenetic analysis results where the subfamilies KLK10 and KLK12 appear as sister groups.
A, Comparison with orphan lizard KLKs and B, Comparison with KLK1. Residues in blue and red background correspond to sites with slower and faster rate of evolution, respectively.
Genomic organization of the putative KLK-encoding genes
Inspection of the KLK protein sequences (Figure S1) suggests that they have virtually identical splicing patters, with slight deviations though. Several serine protease-encoding genes (toxin from Bushmaster, ) also have essentially the same splice sites with KLKs, where the three invariant catalytic residues are located on separate exons. This leads to the suggestion that the serine proteases evolved from an ancestral trypsin-like protein and have retained the same splicing patterns. Only, plasminogen (PLG)-encoding genes have different splicing patterns when compared to the rest of serine protease-encoding genes prompting that the split between the serine proteases took place at that time point .
The process of gene duplication is essential to the efficient generation of genes with novel or altered functions. When the duplicated gene is fixed to the genome and is functionally preserved by natural selection it may diverge either by neofunctionalization or subfunctionalization. The significance of this process is demonstrated by the widespread existence of gene families. The unique characteristic of co-localization and the large number of members is what makes the KLK gene family ideal for evolutionary studies. For example, MMPs constitute another important gene family (consisting of 25 genes in vertebrates and 24 in humans). MMPs are widely distributed in the animal kingdom and appear to have evolved from a single domain protein which underwent successive rounds of duplication, gene fusion and exon-shuffling. However, in contrast to KLKs, the members of this family are distributed along different chromosomes .
The increased availability of fully sequenced genomes from multiple organisms enabled us to conduct a detailed phylogenetic analysis of KLKs in order to reconstruct the evolutionary history of the KLK family. Contrary to the prevailing notion, in the present investigation it was shown that putative KLKs exist in non-therian species, covering an evolutionary distance from amphibia to eutheria. Previous work  suggested that no KLK genes were present in the genome of chicken, frog, or the song bird zebra finch . However, our detailed analysis showed the existence of a frog (Xenopus tropicalis) KLK gene, confirmed the absence of a KLK-like sequence in chicken (Gallus gallus), but in contrast a KLK homologous sequence in turkey (Meleagris gallopavo) and a partial KLK gene (likely pseudogene) were revealed in zebra finch.
In view of our findings it would also be tempting to speculate that the evolutionary origin of KLKs should be moved further back to the radiation of amphibia (330 mya). Noticeably, despite extensive database searches no piscine, ascidian or insect KLK-related proteins were detected. The importance of our findings has implications for the physiological functions, while evolution of KLKs parallels that of their well-established substrates.
Co-evolution of KLK enzymes and substrates
KLK2, KLK3 and reproductive physiology.
KLK2 and KLK3 genes appeared later in evolution of the KLK gene family. Their functional roles are mainly linked to reproduction and more specifically to liquefaction of semen in humans , . Of great interest is the fact that in gorilla the KLK2 gene is absent (i.e. inactivated due to missing coding exons), as also absent are the KLK2-specific substrates in the seminal clot, i.e. semenogelin I, semenogelin II, and TGM4 (prostate transglutaminase 4) that are inactivated due to premature stop codons. Lack of seminal proteins diminishes the viscosity of semen that is liquefied upon ejaculation, therefore the KLK2 enzymatic activity is not needed in this case , . We have further found that in Macaca mullata (Rhesus monkey), KLK2 has a mutation (active site Asp102Ala) that renders the enzyme inactive as previously reported . This probably reflects differences in semen physiology between Rhesus monkey and humans, in that semen does not liquefy but instead forms a copulatory plug. Rhesus monkeys are polygamous in nature, therefore the presence of copulatory plug is important for sperm competition and mate guarding. On the contrary, gorillas are monogamous in nature and there is no need for mate guarding and sperm competition, therefore the aforementioned genes have been inactivated through selection. In addition, a copulatory plug does not exist in cow which is further characterized by the absence of TGM4 , necessary for semen coagulum formation as well as absence of KLK2 and KLK3 that dissolve the coagulum. Further, absence of TGM4 has been reported in opossum and again we did not find KLK2 and KLK3 genes in opossum . Chimpanzee is another polygamous primate and although the genes encoding for KLK2 and KLK3 have not been deleted in this animal the gene for semenogelin I encodes for a more viscous protein of higher molecular weight compared to humans due to a greater number of repeated units . Finally, in contrast to humans, in rodents, semen forms a hard rubbery plug upon ejaculation (copulatory plug). Rodents are highly polygamous in nature. The seminal vesicles of rats and mice secrete six proteins designated SVS1-6 from which SVS-2-6 are homologues to semenogelins , while semen also contains prostate transglutaminase . These proteins cause plug formation, while absence of KLK2 and KLK3 prevents dissolution of the copulatory plug and, thus, rapid semen liquefaction.
KLK4 and tooth development.
KLK4 is important for proteolysis and degradation of the 32 kDa fragment of enamelin since this procedure provides space for apatite growth. Retention of this fragment disturbs the biomineralization process. Consistently, knockout mice for KLK4 showed abnormalities in teeth maturation  and humans suffering from autosomal recessive hypomaturation amelogenesis imperfecta carry a deactivating mutation in the KLK4 active site residue. Taken together this data indicate the crucial function of KLK4 in teeth development . In KLK4 knockout mice although the enamel layer thickness was normal it was rapidly abraded following weaning even when they were maintained with soft chow .
A very recent study reported that birds lack the enamelin-encoding gene which is in accordance with their lack of dentition . One would expect that KLK4 is unnecessary in these animals; indeed we were unable to detect this gene. Consistently, we showed here that chicken genome encodes a non-functional enamelin pseudogene and no KLK4 or other KLKs . In the same context, the enamelin gene is present in monotremes , and while young animals have rudimentary teeth, adult monotremes lack dentition, and accordingly these animals are characterized by the absence of the KLK4 gene as we could not detected it in platypus (Figure 4). Further, xenathra lack dentition, which renders a KLK4 enzyme unnecessary. Although indeed we could not detect KLK4, the presence of this gene in xenatha can not be definitively excluded due to incomplete contig information for armadillo. In contrast to the KLK4 gene, enamelin gene is conserved in xenarthra .
KLKs and skin desquamation.
It is well established that the skin desquamation process involves a proteolytic cascade, which is initiated by activation of proKLK5 either auto-catalytically  or by matriptase . Subsequently, KLK5 activates proKLK7 and proKLK14. Mature KLK14 enhances proKLK5 activation in a feedback loop. In addition, it was shown recently that KLK5 is able to activate proelastase 2 in vitro indicating that KLK5 could be the physiological activator of proelastase 2 in epidermis . Hyperactivation of KLKs (mainly KLK5 and KLK7) in epidermis has been implicated in pathological over-desquamation, a symptom common to a number of skin diseases, including atopic dermatitis and Netherton syndrome (NS) a rare syndrome of severe ichthyosis caused by mutations in Spink5 gene that encodes LEKTI, a multidomain inhibitor of KLKs and other serine proteases . Spink5−/− mice recapitulate the clinical phenotype of NS  as increased activities of KLK5, KLK7 and KLK14 due to lack of LEKTI result in enhanced proteolysis of their corneodesmosomal protein substrates (i.e. corneodesmosin, desmoglein and desmocollin)  that causes stratum corneum detachment and neonatal death. We found that corneodesmosin, desmoglein and desmocollin are present in platypus (ABU86923, XP_001515334 and XP_001515354, respectively) but in frogs only desmocollin was found (NP_001122136). This indicates that protein substrates that form the outer skin layer have co-evolved with their specific processing enzymes (i.e. KLK) as they are essential for replenishment of the skin surface. It is currently not clear whether the KLK skin cascade emerged in platypus, since we were unable to identify a KLK7 orthologue in platypus but this may be due to incomplete genome sequencing.
It should be noted that frog skin and the skin of amphibia, in general, is more permeable than that of mammals since it is engaged in respiration and regulation of internal water and ion loss . For example, stratum corneum of frog epidermis is by 10 times thinner than that of pig . Also, it should be noted that the stratum corneum originally appeared in amphibia and it was essential for terrestrial survival. Further, mouse skin is by 3 times less permeable than that of humans . Interestingly, while human SPINK5 encodes for LEKTI that contains 15 protease inhibitory domains, mouse and rat Spink5 encode for LEKTI that contains only 14 domains and lacks domain 6 , the high-affinity inhibitor of KLK5 and 7 . Therefore, it is expected that higher activity of KLK5 and KLK7 would be found in rodent skin compared to humans, which is compatible with its higher permeability due to increased desquamation. On the other hand, Anolis carolinensis (and generally lizards) has low-permeability skin. While putative orthologs for desmocollin (ENSACAG00000017830) and desmoglein (ENSACAG000000 17850) are encoded in lizards, the absence of KLK5 and KLK7 is compatible with decreased skin shedding and the low permeability of their stratum corneum. Additionally, skin permeability is also decreased by expression of hard-beta keratins and high amounts of lipids that “insulate” the skin .
KLK1 loop-99 and adaptation to increased enzymatic activity
The loop-99 (starting at amino acid residue 99) is necessary for kininogenase activity and is present only in KLK1, KLK2 and PSA/KLK3 . KLK1 is the prototypic kininogenase enzyme that cleaves low molecular-weight kininogen to release bradykinin. As shown in our analysis KLK1 appeared first in amphibia. Interestingly, Kita et al.  have reported the identification of a toxin in blarina, termed BLTX (blarina toxin), that displays high amino acid identity to human KLK1 (55.5 %). Recently, it was reported that amino acid substitutions and insertions mainly in the kallikrein loop are responsible for enhanced kininogenase activity that is expected to release increased amounts of bradykinin associated with toxicity . We have determined in our phylogenetic analysis (data not shown) that Blarina toxin sorts into the KLK1 branch. Very recently, the presence in the platypus venom of an unknown enzyme with kininogenase activity was described . It would be of particular interest, both from the physiological and evolutionary point of view, to determine the sequence of this enzyme and compare its structure with that of the KLK family members of platypus.
Co-expression patterns of evolutionarily related KLKs and (patho)physiological functions
There is ample evidence that duplicated KLKs (i.e. KLK2 and KLK3, KLK4 and KLK5, KLK9 and KLK11, KLK10 and KLK12) are coordinately regulated in biological fluids and tissues, while they often display common patterns of aberrant expression in disease states . For example, KLK9 and KLK11 are highly expressed in esophagus, vagina, stomach, breast, salivary gland and pancreas, KLK4 and KLK5 are highly co-expressed in breast and cervix, KLK10 and KLK12 in salivary gland, esophagus, fallopian tube, and pancreas , . In this context, high levels of KLK5, 6, 7, 10, 12 and 13 have been detected in cervicovaginal fluid indicating potential role in cervical mucous remodeling and vagina epithelial desquamation , . On the other hand, coordinated up-regulation of KLK5, 6, 7, 8, 10, 11 and 14 in ovarian cancer  and down-regulation of KLK5, 6, 8, and 10 in breast cancer  has been observed. KLK tissue-specific co-expression supports the hypothesis that each KLK gene is independently regulated by conserved regulatory mechanisms of transcription. Regulatory involvement of a locus control region (LCR) is not likely as the KLK locus evolved through a series of gene duplication events. Lack of a LCR is corroborated by studies showing that in transgenic mice bearing genomic fragment combinations of 2–3 neighboring rat Klk genes, rat-tissue KLK expression patterns are preserved .
Recent functional studies implicate certain KLKs in various types of cancer , , . For example, in prostate cancer cells, expression of KLK3 and KLK4 results in loss of E-cadherin and induction of expression of the mesenchymal marker vimentin, a hallmark of epithelial-to-mesenchymal transitions, which is a critical step for cancer metastasis . In contrast, re-expression of KLK6 at physiological concentrations dramatically inhibits the growth of primary breast tumors and causes marked reduction of vimentin . Notably, KLK6 is known to be involved in demyelination by cleaving myelin basic protein  and to mediate E-cadherin shedding associated with wound healing in vivo . Interestingly, certain KLKs may exert antiangiogenic functions, since they have been shown to release angiostatin-like peptides by proteolytic processing of plasminogen . Recently, KLKs have emerged as versatile signaling molecules, since they were shown to act as activators of protease-activated receptors (PARs)  and the alpha(5)beta(1) integrin pathway .
The fact that, during the course of evolution, KLKs have survived with significant similarity in terms of sequence, gene organization and number in higher organisms (from monotremes to primates) suggests that they likely play important roles in normal physiology. Elucidating the evolutionary history of KLKs would serve in the development of model systems for the study of gene function(s) in future studies. Collectively, the biological functions of the extended KLK family are currently under investigation. Pleiotropic physiological roles of KLK enzymes are being revealed, while aberrant regulation of KLKs is implicated in diverse diseases such as hypertension, renal dysfunction, skin disorders, inflammation, neurodegeneration, and cancer . Experimental studies should be directed towards deciphering the biochemical function(s) of the putative KLK proteins.
Sequence database searching
In order to identify KLK orthologues, a combination of queries based on key terms and BLAST searches was employed. The names and/or accession numbers of the characterized kallikreins, including all human, mouse and rat KLKs, as well as the canine and equine prostate-specific antigen (KLK3), were used to retrieve their corresponding amino acid sequences. Then, the entire peptide sequences of those KLKs were used as probes to search the publicly available non-redundant databases, UniProt , GenBank  and Ensembl  applying reciprocal BLASTp and tBLASTn  (all E-values were below 1.0E-90). This process was reiterated until no novel sequences could be detected, ensuring that a full representation of the KLK family is obtained.
Primary sequence analysis
The consensus boundaries of the core trypsin domain in the sequences included in the phylogenetic analyses, were determined from full-length sequences combining the outputs of Pfam , SMART , CD-Search ,  and ScanProsite  protein domain prediction search engines. Moreover, using the FingerPRINTScan  search engine, a significant match to all three signature motifs held in PRINTS for the trypsin domain family was found. The sequences of these three conserved motifs for the human, opossum, platypus, lizard and frog KLK homologous proteins were used as input to Weblogo  to produce a consensus sequence for the three KLK catalytic motifs.
Secondary structure prediction
The secondary structure of the identified putative KLK homologous proteins was predicted as a consensus (i.e. 3 out of 5 predictions) of the combined output of CDM , Jpred3 , Porter , PSIPRED  and SSpro . The novel KLK amino acid sequences were aligned along with three KLKs with resolved tree-dimensional structure using PROMALS3D , , a multiple sequence alignment program which incorporates structural information in order to improve alignment accuracy.
Tertiary structure analysis
The program ConSurf  was employed to estimate the degree of conservation of amino acid residues of putative KLKs. For this purpose, the multiple sequence alignment output of the entire KLK homologous amino acid sequences analyzed in this study was used as input to the program to project the conservation grades of residues on the known three-dimensional structure of the human proKLK6 (PDB ID: 1gvl) . For molecular modeling the PyMol molecular graphics program was used.
The predicted core trypsin domain was excised from the full-length peptide sequence analyzed here. The cropped sequences were subsequently aligned using MUSCLE  and phylogenetic trees were reconstructed by employing PhyML , , a maximum likelihood (ML)-based program which optimizes a seed Neighbor-Joining tree by using a simple hillclimbing algorithm. The LG  amino acid substitution model was used. Bootstrap analysis (500 replicates) was performed to test the robustness of the inferred trees. The resulting phylogenetic trees were visualized with Dendroscope .
Chromosomal positioning of KLK genes
Genomic organization of putative KLK homologues
The genomic organization of putative KLK-encoding genes was analyzed by identifying the boundaries between the exons encoding the core trypsin domain of the KLK homologous proteins. The exon-intron boundaries were identified in ENSEMBL. The splice sites were also verified using the core domain of the amino acid sequences shown in Figure S1 as seeds in a tBLASTn search against their respective genomes. The consecutive encoding exons were retrieved in this way. The splicing patterns of several other genes coding for serine proteases such as trypsins, chymotrypsins, CFD, and plasminogens (PLG)  and KLK-like toxin  were also analyzed.
Rate shift analysis
Exon-exon structure of KLKs. Multiple alignment of the amino acid sequences corresponding to the core trypsin domain of KLKs and other serine proteases. The sequences were aligned using MUSCLE. The numbers refer to the amino acid positions with respect to the starting position of the core domain. The spice sites are denoted at the beginning of the respective exons as white letters in a black background. The exon boundaries of particular note are shown in a magenta background. The three catalytic triad residues are shown in blue and the glycine residue in green.
(0.02 MB PDF)
ML phylogram of KLK homologues and related proteins. The CFD/Adipsin sequences were included in the phylogenetic analysis as well. The sequences which are subject to question are indicated by arrows. Conventions are the same as in Figure 7.
(0.26 MB TIF)
Rate shift analysis of KLK7, 10, and 12 subfamilies. The analysis further supports our phylogenetic analysis by demonstrating that KLK10 and KLK12 subfamilies are sister groups.
(5.08 MB TIF)
Names and accession numbers of the sequences analyzed in the present study. The KLK pseudogene names are shown in italics.
(0.32 MB DOC)
Conceived and designed the experiments: AP GS. Performed the experiments: AP. Analyzed the data: AP GP IM GS. Contributed reagents/materials/analysis tools: GS. Wrote the paper: AP GP GS.
- 1. Borgoño CA, Diamandis EP (2004) The emerging roles of human tissue kallikreins in cancer. Nat Rev Cancer 4: 876–890.
- 2. Lilja H, Ulmert D, Vickers AJ (2008) Prostate-specific antigen and prostate cancer: prediction, detection and monitoring. Nat Rev Cancer 8: 268–278.
- 3. Lundwall A, Band V, Blaber M, Clements JA, Courty Y, et al. (2006) A comprehensive nomenclature for serine proteases with homology to tissue kallikreins. Biol Chem 387: 637–641.
- 4. Sotiropoulou G, Pampalakis G, Diamandis EP (2009) Functional roles of human kallikrein-related peptidases. J Biol Chem 284: 32989–32994.
- 5. Lundwall A, Brattsand M (2008) Kallikrein-related peptidases. Cell Mol Life Sci 65: 2019–2038.
- 6. Schmidt AE, Ogawa T, Gailani D, Bajaj SP (2004) Structural role of Gly(193) in serine proteases: investigations of a G555E (GLY193 in chymotrypsin) mutant of blood coagulation factor XI. J Biol Chem 279: 29485–29492.
- 7. Lawrence MG, Lai J, Clements JA (2010) Kallikreins on steroids: structure, function, and hormonal regulation of prostate-specific antigen and the extended kallikrein locus. Endocr Rev. In press.
- 8. Shaw JL, Diamandis EP (2007) Distribution of 15 human kallikreins in tissues and biological fluids. Clin Chem 53: 1423–1432.
- 9. Pampalakis G, Sotiropoulou G (2007) Tissue kallikrein proteolytic cascade pathways in normal physiology and cancer. Biochim Biophys Acta 1776: 22–31.
- 10. Komatsu N, Takata M, Otsuki N, Ohka R, Amano O, et al. (2002) Elevated stratum corneum hydrolytic activity in Netherton syndrome suggests an inhibitory regulation of desquamation by SPINK5-derived peptides. J Invest Dermatol 118: 436–443.
- 11. Caubet C, Jonca N, Brattsand M, Guerrin M, Bernard D, et al. (2004) Degradation of corneodesmosome proteins by two serine proteases of the kallikrein family, SCTE/KLK5/hK5 and SCCE/KLK7/hK7. J Invest Dermatol 122: 1235–1244.
- 12. Descargues P, Deraison C, Bonnart C, Kreft M, Kishibe M, et al. (2005) Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity. Nat Genet 37: 56–65.
- 13. Egelrud T, Brattsand M, Kreutzmann P, Walden K, Vitzithum M, et al. (2005) hK5 and hK7, two serine proteinases abundant in human skin, are inhibited by LEKTI domain 6. Br J Dermatol 153: 1200–1203.
- 14. Olsson AY, Lundwall A (2002) Organization and evolution of the glandular kallikrein locus in Mus musculus. Biochem Biophys Res Commun 299: 305–311.
- 15. Evans BA, Drinkwater CC, Richards RI (1987) Mouse glandural kallikrein genes. Structure and partial sequence analysis of the kallikrein gene locus. J Biol Chem 262: 8027–8034.
- 16. Wines DR, Brady JM, Pritehett DB, Roberts JL, MacDonald RJ (1989) Organization and expression of the rat kallikrein gene family. J Biol Chem 264: 7653–7662.
- 17. Olsson AY, Lilja H, Lundwall A (2004) Taxon-specific evolution of glandular kallikrein genes and identification of a progenitor of prostate-specific antigen. Genomics 84: 147–156.
- 18. Fernando SC, Najar FZ, Guo X, Zhou L, Fu Y, et al. (2007) Porcine kallikrein gene family: genomic structure, mapping, and differential expression analysis. Genomics 89: 429–438.
- 19. Fanhestock M (1994) Characterization of kallikrein cDNAs form the African rodent Mastomys. DNA Cell Biol 13: 293–300.
- 20. Lin FK, Lin CH, Chou CC, Chen K, Lu HS, et al. (1993) Molecular cloning and sequence analysis of the monkey and human tissue kallikrein genes. Biochim Biophys Acta 1173: 325–328.
- 21. Gauthier ER, Chapdelaine P, Tremblay RR, Dube JY (1993) Characterization of rhesus monkey prostate specific antigen cDNA. Biochim Biophys Acta 1174: 207–210.
- 22. Pampalakis G, Arampatzidou M, Amoutzias G, Kossida S, Sotiropoulou G (2008) Identification and analysis of mammalian KLK6 orthologue genes for prediction of physiological substrates. Comput Biol Chem 32: 111–121.
- 23. Chapdelaine P, Gauthier E, Ho-Kim MA, Bissonnette L, Tremblay RR, et al. (1991) Characterization and expression of the prostatic arginine esterase gene, a canine glandular kallikrein. DNA Cell Biol 10: 49–59.
- 24. Fiedler F, Betz G, Hinz H, Lottspeich F, Raidoo DM, et al. (1999) Not more that three tissue kallikreins indentified from organs of the guinea pig. Biol Chem 380: 63–73.
- 25. Karr JF, Kantor JA, Hand PH, Eggensperger DL, Scholm J (1995) The presence of prostate-specific antigen-related genes in primates and the expression of recombinant human prostate-specific antigen in a transfected murine cell line. Cancer Res 55: 2455–2462.
- 26. Fujimori H, Levison PR, Schachter M (1986) Purification and partial characterization of cat pancreatic and urinary kallikreins-comparison with other cat tissue kallikreins and related proteases. Adv Exp Med Biol 198 (Pt A): 219–228.
- 27. Olsson AY, Valtonen-Andre C, Lilja H, Lundwall A (2004) The evolution of the glandular kallikrein locus: identification of orthologs and pseudogenes in the cotton-tap tamarin. Gene 343: 347–355.
- 28. Elliott MB, Irwin DM, Diamandis EP (2006) In silico identification and Bayesian phylogenetic analysis of multiple new mammalian kallikrein gene families. Genomics 88: 591–599.
- 29. Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, et al. (2006) Database resources of the National Center for Biotechnology Information. Nucleic Acids Res 34: D173–180.
- 30. Warren WC, Clayton DF, Ellegren H, Arnold AP, Hillier LW, et al. (2010) The genome of a songbird. Nature 464: 757–762.
- 31. Warren WC, Hillier LW, Marshall Graves JA, Birney E, et al. (2008) Genome analysis of the platypus reveals unique signatures of evolution. Nature 453: 175–183.
- 32. Yoon H, Blaber SI, Debela M, Goettig P, Scarisbrick IA, et al. (2009) A completed KLK activome profile: investigation of activation profiles of KLK9, 10, and 15. Biol Chem 390: 373–377.
- 33. Kim WS, Nakayama K, Nakagawa T, Kamamoura Y, Haraguchi K, et al. (1991) Mouse submandibular gland prorenin-converting enzyme is a member of glandula kallikrein family. J Biol Chem 266: 19282–19287.
- 34. Gomis-Ruth FX, Bayés A, Sotiropoulou G, Pampalakis G, Tsetsenis T, et al. (2002) The structure of human prokallikrein 6 reveals a novel activation mechanism for the kallikrein family. J Biol Chem 277: 27273–27281.
- 35. Laxmikanthan G, Blaber SI, Bernett MJ, Scarisbrick IA, Juliano MA, et al. (2005) 1.70 A X-ray structure of human apo kallikrein 1: structural changes upon peptide inhibitor/substrate binding. Proteins 58: 802–814.
- 36. Debela M, Goettig P, Magdolen V, Huber R, Schechter NM, et al. (2007) Structural basis of the zinc inhibition of human tissue kallikrein 5. J Mol Biol 373: 1017–1031.
- 37. Puente XS, Lopéz-Otín C (2004) A genomic analysis of rat proteases and protease inhibitors. Genome Res 14: 609–622.
- 38. Hallstrom BM, Kullberg M, Nilsson MA, Janke A (2007) Phylogenomic data analyses provide evidence that Xenarthra and Afrotheria are sister groups. Mol Biol Evol 24: 2059–2068.
- 39. Nikolaev S, Montoya-Burgos JI, Margulies EH, Rougemont J, Nyffeler B, et al. (2007) Early history of mammals is elucidated with the ENCODE multiple species sequencing data. PLoS Genet 3: e2.
- 40. Clark NL, Swanson WJ (2005) Pervasive adaptive evolution in primate seminal proteins. Plos Genet 1: e35.
- 41. Carvalho AL, Sanz L, Barettino D, Romero A, Calvete JJ, et al. (2002) Crystal structure of a prostate kallikrein isolated from stallion seminal plasma: a homologue of human PSA. J Mol Biol 322: 325–337.
- 42. Lovgren J, Rajakoski K, Karp M, Lundwall A, Lilja H (1997) Activation of the zymogen form of prostate-specific antigen by human glandular kallikrein 2. Biochem Biophys Res Commun 238: 549–555.
- 43. Zhang P, Zhou H, Chen YQ, Liu YF, Qu LH (2005) Mitogenomic perspectives on the origin and phylogeny of living amphibia. Syst Biol 54: 391–400.
- 44. Kong HJ, Hong GE, Nam BH, Kim YO, Kim WJ, et al. (2009) An immune responsive complement factor D/adipsin and kallikrein-like serine protease (PoDAK) from the olive flounder Paralichthys olivaceus. Fish Shellfish Immunol 27: 486–492.
- 45. Fantuzzi G (2005) Adipose tissue, adipokines, and inflammation. J Allergy Clin Immunol 115: 911–919; quiz 920.
- 46. Rosen BS, Cook KS, Yaglom J, Groves DL, Volanakis JE, et al. (1989) Adipsin and complement factor D activity: an immune-related defect in obesity. Science 244: 1483–1487.
- 47. Knudsen B, Miyamoto MM (2001) A likelihood ratio test for evolutionary rate shifts and functional divergence among proteins. Proc Natl Acad Sci USA 98: 14512–14517.
- 48. Giovanni-De-Simone S, Aguiar AS, Gimenez AR, Novellino K, de Moura RS (1997) Purification, properties, and N-terminal amino acid sequence of a kallikrein-like enzyme from the venom of Lachesis muta rhombeata (Bushmaster). J Protein Chem 16: 809–818.
- 49. Forsgren M, Raden B, Israelsson M, Larsson K, Heden LO (1987) Molecular cloning and characterization of a full-length cDNA clone for human plasminogen. FEBS Lett 213: 254–260.
- 50. Fanjul-Fernadez M, Folgueras AR, Cabrera S, López-Otín C (2010) Matrix metalloproteinases: evolution, gene regulation and functional analysis in mouse models. Biochim Biophys Acta 1803: 3–19.
- 51. Quesada V, Velasco G, Puente XS, Warren WC, Lopéz-Otín C (2010) Comparative genomic analysis of the zebra finch degradome provides new insights into evolution of proteases in birds and mammals. BMC Genomics 11: 220.
- 52. Jensen-Seaman MI, Li WH (2003) Evolution of the hominoid semenogelin genes, the major proteins of ejaculated semen. J Mol Evol 57: 261–270.
- 53. Tian X, Pascal G, Fouchecourt S, Pontarotti P, Monget P (2009) Gene birth, death and divergence: the different scenarios of reproduction-related gene evolution. Biol Reprod 80: 616–621.
- 54. Lundwall A, Lazure C (1995) A novel gene family encoding proteins with highly differing structure because of a rapidly evolving exon. FEBS Lett 374: 53–56.
- 55. Simmer JP, Hu Y, Lertlam R, Yamakoshi Y, Hu JCC (2009) Hypomaturation enamel defects in Klk4 knockout/LacZ knockin mice. J Biol Chem 284: 19110–19121.
- 56. Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, et al. (2004) J Med Genet 41: 545–549.
- 57. Al-Hashimi N, Lafont AG, Delgado S, Kawasaki K, Sire JY (2010) The enamelin genes in lizard, crocodile and frog, and the pseudogene in chicken provide insights on enamel evolution in tetrapods. Mol Biol Evol (in press).
- 58. Al-Hashimi N, Sire JY, Delgado S (2009) Evolutionary analysis of mammalian enamelin, the largest enamel protein, supports a crucial role for the 32-kDa peptide and reveals selective adaptation in rodents and primates. J Mol Evol 69: 635–656.
- 59. Brattsand M, Stefansson K, Lundh C, Haasum Y, Egelrud T (2005) A proteolytic cascade of kallikreins in the stratum corneum. J Invest Dermatol 124: 198–203.
- 60. Sales KU, Masedunskas A, Bey AL, Rasmussen AL, Weigert R, et al. (2010) Matriptase initiates activation of epidermal pro-kallikrein and disease onset in a mouse model of Netherton syndrome. Nat Genet 42: 676–683.
- 61. Bonnart C, Deraison C, Lacroix M, Uchida Y, Besson C, et al. (2010) Elastase 2 is expressed in human and mouse epidermis and impairs skin barrier function in Netherton syndrome through filaggrin and lipid misprocessing. J Clin Invest 120: 871–882.
- 62. Descargues P, Deraison C, Bonnart C, Kreft M, Kishibe M, et al. (2005) Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity. Nat Genet 56-65:
- 63. Borgoño CA, Michael IP, Komatsu N, Jayakumar A, Kapadia R, et al. (2007) A potential role for multiple tissue kallikrein serine proteases in epidermal desquamation. J Biol Chem 282: 3640–3652.
- 64. Quaranta A, Bellantuono V, Cassano G, Lippe C (2009) Why amphibians are more sensitive than mammals to xenobiotics. PLoS ONE 4: e7699.
- 65. Lillywhite HB (2006) Water relations of tetrapod integument. J Exp Biol 209: 202–226.
- 66. Galliano MF, Roccasecca RM, Descargues P, Micheloni A, Levy E, et al. (2005) Characterization and expression analysis of the Spink5 gene, the mouse ortholog of the defective gene in Netherton syndrome. Genomics 85: 483–492.
- 67. Kita M, Nakamura Y, Okumura Y, Ohdachi SD, Oba YM, et al. (2005) Blarina toxin, a mammalian lethal venom from the short-tailed shrew Blarina brevicauda: Isolation and characterization. Proc Natl Acad Sci 101: 7542–7547.
- 68. Aminetzach YT, Srouji JR, Kong CY, Hoekstra HE (2009) Convergent evolution of novel protein function in shrew and lizard venom. Curr Biol 19: 1925–1931.
- 69. Kita M, Black DStC, Ohno O, Yamada K, Kigoshi H, et al. (2009) Duck-billed platypus venom peptides induce Ca2+ influx in neuroblastoma cells. J Am Chem Soc 131: 13038–13039.
- 70. Shaw JLV, Diamandis EP (2007) Distribution of 15 human kallikreins in tissues and biological fluids. Clin Chem 53: 1423–1432.
- 71. Harvey TJ, Hooper JD, Myers SA, Stephenson SA, Ashworth LK, et al. (2000) Tissue-specific expression patterns and fine mapping of the human kallikrein (KLK) locus on proximal 19q13.4. J Biol Chem 275: 37397–37406.
- 72. Shaw JL, Smith CR, Diamandis EP (2007) Proteomic analysis of human cervico-vaginal fluid. J Proteome Res 6: 2859–2865.
- 73. Shaw JL, Petraki C, Watson C, Bocking A, Diamandis EP (2008) Role of tissue kallikrein-related peptidases in cervical mucus remodelling and host defense. Biol Chem 389: 1513–1522.
- 74. Yousef GM, Polymeris ME, Yacoub GM, Scorilas A, Soosaipillai A, et al. (2003) Parallel overexpression of seven kallikrein genes in ovarian cancer. Cancer Res 63: 2223–2227.
- 75. Yousef GM, Yacoub GM, Polymeris ME, Popalis C, Soosaipillai A, et al. (2004) Kallikrein gene downregulation in breast cancer. Br J Cancer 90: 167–172.
- 76. Kroon E, MacDonald RJ, Hammer RE (1997) The transcriptional regulatory strategy of the rat tissue kallikrein gene family. Genes Funct 1: 309–319.
- 77. Veveris-Lowe TL, Lawrence MG, Collard RL, Bui L, Herington AC, et al. (2005) Endocr Relat Cancer 12: 631–643.
- 78. Pampalakis G, Prosnikli E, Agalioti T, Vlahou A, Zoumpourlis V, et al. (2009) A tumor protective role for human kallikrein-related peptidase 6 in breast cancer mediated by inhibition of epithelial-to-mesenchymal transition. Cancer Res 69: 3779–1787.
- 79. Bernett MJ, Blaber SI, Scarisbrick IA, Dhanarajan P, Thompson SM, et al. (2002) Crystal structure and biochemical characterization of human kallikrein 6 reveals that a trypsin-like kallikrein is expressed in the central nervous system. J Biol Chem 277: 24562–24570.
- 80. Klucky B, Mueller R, Vogt I, Teurich S, Hartenstein B, et al. (2007) Kallikrein 6 induces E-cadherin shedding and promotes cell proliferation, migration, and invasion. Cancer Res 67: 8198–8206.
- 81. Sotiropoulou G, Rogakos V, Tsetsenis T, Pampalakis G, Zafeiropoulos N, et al. (2003) Emerging interest in the kallikrein gene family for understanding and diagnosing cancer. Oncol Res 13: 381–391.
- 82. Oikonomopoulou K, Hansen KK, Saifeddine M, Tea I, Blaber M, et al. (2006) J Biol Chem 281: 32095–32112.
- 83. Dong Y, Tan OL, Loessner D, Stephens C, Walpole C, et al. (2010) Kallikrein-related peptidase 7 promotes multicellular aggregation via the alpha(5)beta(1) integrin pathway and paclitaxel chemoresistance in serous epithelial ovarian carcinoma. Cancer Res 70: 2624–2633.
- 84. Bairoch A, Apweiler R, Wu CH, Barker WC, Boeckmann B, et al. (2005) The Universal Protein Resource (UniProt). Nucleic Acids Res 33: D154–159.
- 85. Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Sayers EW (2009) GenBank. Nucleic Acids Res 37: D26–31.
- 86. Hubbard TJ, Aken BL, Ayling S, Ballester B, Beal K, et al. (2009) Ensembl 2009. Nucleic Acids Res 37: D690–697.
- 87. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215: 403–410.
- 88. Finn RD, Tate J, Mistry J, Coggill PC, Sammut SJ, et al. (2008) The Pfam protein families database. Nucleic Acids Res 36: D281–288.
- 89. Letunic I, Doerks T, Bork P (2009) SMART 6: recent updates and new developments. Nucleic Acids Res 37: D229–232.
- 90. Fong JH, Marchler-Bauer A (2008) Protein subfamily assignment using the Conserved Domain Database. BMC Res Notes 1: 114.
- 91. Marchler-Bauer A, Anderson JB, Chitsaz F, Derbyshire MK, DeWeese-Scott C, et al. (2009) CDD: specific functional annotation with the Conserved Domain Database. Nucleic Acids Res 37: D205–210.
- 92. de Castro E, Sigrist CJ, Gattiker A, Bulliard V, Langendijk-Genevaux PS, et al. (2006) ScanProsite: detection of PROSITE signature matches and ProRule-associated functional and structural residues in proteins. Nucleic Acids Res 34: W362–365.
- 93. Scordis P, Flower DR, Attwood TK (1999) FingerPRINTScan: intelligent searching of the PRINTS motif database. Bioinformatics 15: 799–806.
- 94. Crooks GE, Hon G, Chandonia JM, Brenner SE (2004) WebLogo: a sequence logo generator. Genome Res 14: 1188–1190.
- 95. Cheng H, Sen TZ, Jernigan RL, Kloczkowski A (2007) Consensus Data Mining (CDM) Protein Secondary Structure Prediction Server: combining GOR V and Fragment Database Mining (FDM). Bioinformatics 23: 2628–2630.
- 96. Cole C, Barber JD, Barton GJ (2008) The Jpred 3 secondary structure prediction server. Nucleic Acids Res 36: W197–201.
- 97. Pollastri G, McLysaght A (2005) Porter: a new, accurate server for protein secondary structure prediction. Bioinformatics 21: 1719–1720.
- 98. McGuffin LJ, Bryson K, Jones DT (2000) The PSIPRED protein structure prediction server. Bioinformatics 16: 404–405.
- 99. Cheng J, Randall AZ, Sweredoski MJ, Baldi P (2005) SCRATCH: a protein structure and structural feature prediction server. Nucleic Acids Res 33: W72–76.
- 100. Pei J, Kim BH, Grishin NV (2008) PROMALS3D: a tool for multiple protein sequence and structure alignments. Nucleic Acids Res 36: 2295–2300.
- 101. Pei J, Tang M, Grishin NV (2008) PROMALS3D web server for accurate multiple protein sequence and structure alignments. Nucleic Acids Res 36: W30–34.
- 102. Landau M, Mayrose I, Rosenberg Y, Glaser F, Martz E, et al. (2005) ConSurf 2005: the projection of evolutionary conservation scores of residues on protein structures. Nucleic Acids Res 33: W299–302.
- 103. Edgar RC (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32: 1792–1797.
- 104. Guindon S, Gascuel O (2003) A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 52: 696–704.
- 105. Guindon S, Lethiec F, Duroux P, Gascuel O (2005) PHYML Online--a web server for fast maximum likelihood-based phylogenetic inference. Nucleic Acids Res 33: W557–559.
- 106. Le SQ, Gascuel O (2008) An improved general amino acid replacement matrix. Mol Biol Evol 25: 1307–1320.
- 107. Huson DH, Richter DC, Rausch C, Dezulian T, Franz M, et al. (2007) Dendroscope: An interactive viewer for large phylogenetic trees. BMC Bioinformatics 8: 460.
- 108. Wolfsberg TG (2007) Using the NCBI Map Viewer to browse genomic sequence data. Curr Protoc Bioinformatics Chapter 1: Unit 1 5.