Figures
Abstract
Some cyanobacteria are capable of differentiating a variety of cell types in response to environmental factors. For instance, in low nitrogen conditions, some cyanobacteria form heterocysts, which are specialized for N2 fixation. Many heterocyst-forming cyanobacteria have DNA elements interrupting key N2 fixation genes, elements that are excised during heterocyst differentiation. While the mechanism for the excision of the element has been well-studied, many questions remain regarding the introduction of the elements into the cyanobacterial lineage and whether they have been retained ever since or have been lost and reintroduced. To examine the evolutionary relationships and possible function of DNA sequences that interrupt genes of heterocyst-forming cyanobacteria, we identified and compared 101 interruption element sequences within genes from 38 heterocyst-forming cyanobacterial genomes. The interruption element lengths ranged from about 1 kb (the minimum able to encode the recombinase responsible for element excision), up to nearly 1 Mb. The recombinase gene sequences served as genetic markers that were common across the interruption elements and were used to track element evolution. Elements were found that interrupted 22 different orthologs, only five of which had been previously observed to be interrupted by an element. Most of the newly identified interrupted orthologs encode proteins that have been shown to have heterocyst-specific activity. However, the presence of interruption elements within genes with no known role in N2 fixation, as well as in three non-heterocyst-forming cyanobacteria, indicates that the processes that trigger the excision of elements may not be limited to heterocyst development or that the elements move randomly within genomes. This comprehensive analysis provides the framework to study the history and behavior of these unique sequences, and offers new insight regarding the frequency and persistence of interruption elements in heterocyst-forming cyanobacteria.
Citation: Hilton JA, Meeks JC, Zehr JP (2016) Surveying DNA Elements within Functional Genes of Heterocyst-Forming Cyanobacteria. PLoS ONE 11(5): e0156034. https://doi.org/10.1371/journal.pone.0156034
Editor: Franck Chauvat, CEA-Saclay, FRANCE
Received: July 17, 2015; Accepted: April 14, 2016; Published: May 20, 2016
Copyright: © 2016 Hilton 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.
Data Availability: All previously-published genomic sequences are available from the NCBI and JGI databases as specified in S1 Table, and the relevant sequences from the Calothrix rhizosoleniae SC01 genome are within the Supporting Information files of this paper.
Funding: This work was sponsored in part by a Gordon and Betty Moore Foundation Investigator award (#493.01, J.P.Z.) and the National Science Foundation Center for Microbial Oceanography: Research and Education (EF0424599, J.P.Z.).
Competing interests: The authors have declared that no competing interests exist.
Introduction
Cyanobacteria can alter their cell shape and size, cell wall thickness, and filament orientation in response to environmental conditions varying from nutrient limitation to predation [1–3]. The morphological diversity of cyanobacteria also extends to cell differentiation as some filamentous cyanobacteria can form akinetes, hormogonia, and heterocysts, in addition to vegetative cells. Akinetes are spore-like cells formed during unfavorable growth conditions [4], while hormogonia are small-celled, motile filaments that are especially important in symbiosis initiation [5]. Heterocysts are the sites of N2 fixation under nitrogen (N) limitation [6].
N2 fixation, the process of converting N2 to NH3, can be a means of avoiding a common nutrient limitation for microbial growth in a variety of environments [7,8]. Nitrogenase, the enzyme that catalyzes N2 fixation, is sensitive to inactivation by oxygen (O2) [9], and must withstand the O2 that is in the environment and that evolves through photosynthesis. Heterocysts create and maintain a microoxic microenvironment by shutting down the activity of O2-evolving photosystem II, increasing respiratory O2 uptake, and creating a thick envelope around the cell wall to restrict gas diffusion [6].
Heterocyst differentiation is regulated by many signaling pathways [10] and is accompanied by the changes in the expression of 500 to 1,000 genes [11,12]. In some heterocyst-forming cyanobacteria, genome rearrangement is also necessary in order to form fully functional heterocysts. Key N2 fixation genes are often interrupted in the genome of vegetative cells by DNA sequences, referred to herein as interruption elements, previously observed to be as long as 80 kb in length [13]. Excision of an interruption element during heterocyst formation results in a contiguous, functional gene in heterocyst genomes [14] (Fig 1). These elements are not in all heterocyst-forming cyanobacterial genomes, but have been commonly found within hupL, which encodes one subunit of an uptake hydrogenase responsible for recycling hydrogen (H2) produced during N2 fixation, and nifD, which encodes the nitrogenase alpha subunit [13–18]. Additionally, elements have been reported within fdxN, which encodes a ferredoxin and is located in an operon with nitrogenase genes nifU, nifS, and nifB, and likely nifH, nifD, and nifK, as well. [14,15,17,19,20]. More recently, elements have been found in the nitrogenase iron subunit gene nifH, and in nifK, the nitrogenase beta subunit gene [13,21,22].
An example of an element interrupting a gene (split into coxA31 and coxA32) in the vegetative genome. The complete, functional coxA3 gene is present in the heterocyst genome due to the element excision by the protein encoded by the xis gene.
The elements are removed during the later stages of heterocyst development by a site-specific recombinase, which is encoded by a gene located within the element [15,23]. To excise the interruption element, the recombinase binds to direct repeats that bracket the element [24]. Genes for these recombinases have been identified as xisA, xisC, and xisF within nifD, hupL, and fdxN elements, respectively [14,25,26]. The nifH element recombinase gene sequences is most similar to that of xisA [21], and the sequence of the recombinase gene in the nifK element is most closely related to the xisF sequence [22]. xisA expression is likely regulated by the transcriptional regulators for nitrogen, NtcA, and ferric uptake, FurA; however, little is known of the details of the regulatory mechanisms and other potential regulating factors of interruption element recombinases [27–29]. Two additional genes, xisH and xisI, located in the Nostoc sp. strain PCC 7120 (Nostoc 7120) fdxN element are also required for excision of that element [30]. The specific roles of xisH and xisI are unclear, but they may be related to determining the direction of recombination catalyzed by XisF—integration vs. excision [31]. It is also unclear when or how all of these interruption elements originated; it has been hypothesized that they are the remnants of viruses or phages [18,32].
Yet another mystery is whether the elements provide any advantage or disadvantage to heterocyst-forming cyanobacteria or if they are selfish DNA, and have little to no effect(s) on the organisms [33]. The possession or lack of a nifD element did not affect cell growth or N2 fixation of two different Nostoc strains in the presence of combined N or with N2 as the sole N source [34,35]. Thus, the presence or absence of this element has no apparent selective advantage under laboratory growth conditions, at least not within the timescale of these experiments.
In an effort to more fully explore the evolution and potential purposes of the interruption elements, the work presented here examines the elements found in all currently sequenced heterocyst-forming cyanobacterial genomes. We defined 101 interruption elements in heterocyst-forming cyanobacterial genomes, including many previously unknown elements, and compared them in an attempt to determine their evolutionary paths. Additionally, in an effort to provide evolutionary context for these elements, we searched all cyanobacterial genomes for interruption elements and discovered three elements within genes of cyanobacteria that are not capable of forming heterocysts.
Materials and Methods
As of the writing of this report, there were 38 heterocyst-forming cyanobacteria with sequenced genomes; 27 from the order Nostocales and 11 from the order Stigonematales (Fig 2). The Calothrix rhizosoleniae SC01 genome is yet unreleased, but sequences relevant to this study can be found in S1 and S2 Data. Accession numbers for all of the other genomes can be found in Table A in S1 File. Annotations of the genomes were examined, focusing on regions near the five genes previously shown to contain interruption elements (nifH, nifD, nifK, hupL, and fdxN). The gene synteny surrounding each of these genes is highly conserved in heterocyst-forming cyanobacteria. Any genes found between nifH, nifD, nifK, hupL, or fdxN and the expected adjacent gene were examined for the presence of a gene with similarity to one of the known xis genes. A BLAST analysis (blastp) was conducted with these recombinase genes against all protein sequences of the 38 genomes. Each gene with a hit to any of the xis genes (with an in silico-determined threshold e-value ≤10−20) was examined as follows. A BLAST analysis (blastx, e-value ≤10, maximum matches in a query range = 15) was conducted for each xis gene candidate and surrounding nucleotides (3 kb up- and down-stream) against the nr database (NCBI). Genes that were similar to either region flanking the candidate xis gene, but truncated, were used as references for the possible interrupted gene. We then used each reference gene as a query to a BLAST search (tblastn, e-value ≤10) against the entire genome in order to locate sequences similar to different sections of the reference gene. Those genome regions were then aligned with the reference gene to confirm that they formed an interrupted gene. Once aligned, the direct repeats were identified in the overlapping bases of the two genome regions (Fig 1). We did not allow for any mismatches to occur between direct repeats, and thus, these may not represent the entire target sequence, but for the purposes of this study, serve as a marker for the end and beginning of each element. As more interruption elements were confirmed, the xis gene sequences from each were added to the set, and the BLAST analysis was repeated to find more potential gene interruptions and associated xis genes.
Maximum likelihood phylogenetic tree of 16S rRNA from 38 heterocyst-forming cyanobacterial genomes, rooted with Trichodesmium erythraeum IMS 101. The size of the genome and the number of interruption elements within the genome are shown within parentheses. Cyanobacteria of the order Nostocales are in shaded boxes, and all other cyanobacteria belong to the order Stigonematales, with the exception of T. erythraeum IMS101. Open circles at branch connections indicate a bootstrap value of at least 75%.
A BLAST analysis was then conducted with all of the confirmed xis genes from the heterocyst-forming cyanobacterial genomes against all non-heterocyst-forming cyanobacterial genomes (blastp, e-value ≤10−50). More stringent criteria was used for this BLAST analysis in order to limit our results to only those recombinase genes most similar to the known xis genes. All BLAST hits were checked for interrupted genes as described above.
For the recombinase gene and 16S rRNA phylogenetic trees, nucleotide sequences were aligned in MEGA5 with ClustalW [36]. The recombinase gene sequence alignments were done with respect to codons, and thus, no gaps were inserted within a codon. Maximum likelihood phylogenetic trees were constructed with MEGA5 using the Tamura-Nei model and only those alignment sites with at least 90% coverage were used [37]. Statistical support for nodes was based on 1,000 bootstrap replicates [38].
To analyze shared genes within the gene content of the elements, a bi-directional BLAST analysis (blastp, e-value ≤10−20) was conducted on all of the genes from each heterocyst-forming cyanobacterial genome against the full gene set from each of the other genomes. We then identified the genes encoded in an element that had bi-directional best hits to at least four other genes from elements. The bi-directional best hits of each of those genes were then used to identify non-element genes occurring in other genomes.
Results
We identified 101 interruption elements within 28 genomes of heterocyst-forming cyanobacteria, while an additional 10 genomes did not have any observed elements (Fig 2). Five out of 11 cyanobacteria within Stigonematales each had at least one element. On the other hand, 23 out of 27 Nostocales organisms possessed at least one interruption element, with as many as 11 elements in one genome (Calothrix sp. PCC 7103). The structure of the phylogenetic tree generated based on the 16S rRNA sequences of these 38 genomes largely agreed with phylogenetic trees that were made using concatenated gene sequences from many of the same genomes, with the main exception being Anabaena sp. PCC 7108 which has grouped more closely with Anabaena cylindrica PCC 7122 and Nostoc azollae 0708 in other trees [39,40].
The interruption elements were as small as the 1.3 kb element within a Scytonema hofmanni UTEX 2349 FAD-dependent oxidoreductase gene up to the nearly 1 Mb coxA element in Calothrix sp. PCC 6303 (Table B in S1 File). The average element length was 41.5 kb, excluding seven elements that could not be characterized due to apparent genome mis-assembly and nine elements that were predicted from sequences on separate contigs, and thus may be longer than determined by genomic analysis. All of the elements that were found in this study and their xis genes are catalogued fully in Table B in S1 File.
The elements within heterocyst-forming cyanobacterial genomes interrupted 87 individual genes, and 10 of those genes were interrupted by multiple elements. The Rivularia sp. PCC 7116 nifD was interrupted by four different element, the most found within a single gene (Figure A in S2 File). Each of the 87 interrupted genes belonged to one of 22 different ortholog groups, but not all elements within a given ortholog interrupted the gene at the same location (Table 1). We considered all elements that interrupted the same ortholog at roughly the same position along that ortholog (± 10 bp) to represent an element variant. A slight fluctuation in the start positions of direct repeats within a variant was due to the varying lengths of the direct repeat. The 34 nifD elements belonged to four different element variants, while six element variants were found amongst the 19 nifH elements. Two variants each were found for nifK, nifB, hupL, hupS, and coxA3 elements.
The presence of element variants with more than three occurrences in the heterocyst-forming cyanobacterial genomes was plotted along the 16S rRNA phylogeny (Figures B and C in S2 File). The variants range from those organisms possessing them clustering together (e.g. nifH 405 and fdxN) to those that were spread out throughout the 16S rRNA phylogenetic tree (e.g. hupL 590 and nifD 895).
A xis gene was identified for 100 out of the 101 elements (Table B in S1 File). A contig break prevented the confirmation of a recombinase-coding gene in the Richelia intracellularis RC01 nifH element. There were also seven cases that involved the two sections of the interrupted gene oriented in opposite directions (Figure D in S2 File). These are likely due to mis-assembly of the genome, and have been labeled as "odd assembly" in Table B in S1 File. The sequences for the corresponding xis genes were included in phylogenetic analysis but no further characterization of the interruption elements was done. There were 44 additional genes with a BLAST hit to a xis gene (e-value <10−20), but an interrupted gene could not be located near them, and, thus, could not be verified as element excision genes, possibly due to the bias introduced by limiting our search for an interrupted gene to within 3 kb of each possible xis gene.
Of the xis genes found in this study, 48 encoded recombinases belonging to the serine recombinase superfamily, while the remaining 52 encoded recombinases of the tyrosine superfamily (Table B in S1 File). At least one element containing a serine recombinase was found interrupting each of the 22 ortholog groups, but only six ortholog groups had an occurrence of an element containing a tyrosine recombinase. The 23 xis genes aligned in the same orientation as the interrupted genes were located towards the beginning of the element. All but one of the 70 xis genes that were oriented in the opposite direction to the interrupted gene were found closer to the end of the element (example: Fig 1). The xis gene in the Calothrix sp. PCC 6303 arabinose efflux permease interruption element was the exception to this, and although oriented in the opposite direction of the interrupted gene, it was located at the beginning of the element.
The majority of xis gene sequences formed well-supported phylogenetic clusters with other xis genes found in interruption elements of the same element variant (Figs 3 and 4), but there were a few exceptions. The three xis gene sequences of elements that interrupted nifH at position 150 (± 7 bp) were closely-related, but did not form a branch like the xis genes from each of the other variants (Fig 3; Anabaena sp. 90 element #1, Anabaena circinalis AWQC310F #1, and Scytonema hofmanni PCC 7110 #3). The nifD elements with insertion locations at position 895 (± 1 bp) contained xis gene sequences that clustered together, however, four of the genes were within a subcluster with strong bootstrap support (Anabaena cylindrica PCC 7122 #5, Anabaena sp. PCC 7108 #2, Cylindrospermum stagnale PCC 7417 #2, and Microchaete sp. PCC 7126 #2), while the Rivularia sp. PCC 7116 (#6) and Calothrix sp. PCC 7103 (#10) genes were phylogenetically distant (Fig 4). The Rivularia sp. PCC 7116 and Calothrix sp. PCC 7103 xis genes within these elements were located at the end of the element, oriented in the opposite direction as nifD, but the xis genes within the other four elements of this variant were found at the beginning of the element and read in the same direction as nifD. Similarly, the two xis gene sequences from the nifD elements with insertion locations at position 227 clustered together, but exhibited long branch lengths and low bootstrap support, and the xis genes differed in location and orientation (Fig 4; Rivularia sp. PCC 7116 #9 and Calothrix sp. PCC 7103 #11). The flv3B elements of S. hofmanni PCC 7110 and Calothrix rhizosoleniae SC01 also had xis genes of differing location and orientation (Fig 3). The S. hofmanni PCC 7110 xis gene was located at the end of the element and was oriented in the opposite direction of the flv3B that it interrupted, while the C. rhizosoleniae SC01 xis gene was at the beginning of the element and was read in the same direction as flv3B.
Maximum likelihood phylogenetic tree of serine recombinase gene (xis) nucleotide sequences and data characterizing the element each xis gene is found on. Shaded boxes group element variants together. Open circles at branch connections indicate a bootstrap value of at least 75.
Maximum likelihood phylogenetic tree of tyrosine recombinase gene (xis) nucleotide sequences and data characterizing the element each xis gene is found on. Shaded boxes group element variants together. Open circles at branch connections indicate a bootstrap value of at least 75.
In some cases, xis gene sequences grouped phylogenetically by organism. For example, seven genes in the A. cylindrica PCC 7122 were identical to each other, and while no interruption element could be identified for four of the genes, the three other genes were identified as encoding element excision proteins (Fig 3; A. cylindrica PCC 7122 #1–3). Similarly, the xis gene of the interruption element within a S. hofmanni UTEX 2349 transposase was identical to the xis gene in an oxidoreductase gene interruption element in the same genome (Table B in S1 File). However, the oxidoreductase gene interruption element xis gene sequence was shortened by a gap in the genome assembly, and, thus, was left out of the analysis. Although more divergent than the A. cylindrica PCC 7122 and S. hofmanni UTEX 2349 xis genes, the Rivularia sp. PCC 7116 xis gene sequences responsible for the nifB and hupS elements clustered together (Fig 4). The length and GC content of each element was plotted along the xis phylogeny (Figures E-H in S2 File), but no clear patterns emerged.
Seven groups of genes were identified that were shared amongst at least five elements (Table C in S1 File). Four of these gene groups were shared amongst the nifD element variant that interrupts the gene at position 1355 (± 2 bp). These include a hypothetical protein that was found in 17 elements, as well as an ATPase gene that was found exclusively in elements. A hypothetical protein was conserved in five hupL elements and also found in one additional genome not in en element. A translation elongation factor G paralog was found in three different element variants of five genomes and in two other genomes, which have the potential to be in elements, as discussed below. A transposase gene was also found on multiple element variants.
Interruption elements were also found within genes of three unicellular non-heterocyst-forming cyanobacteria, including a hypothetical membrane protein of Chroococcidiopsis thermalis PCC 7203 (Table B in S1 File). A Synechococcus sp. PCC 7502 DNA helicase gene and a Cyanothece sp. PCC 7822 hypothetical protein were also interrupted by interruption elements. The xis gene sequences from these elements were spread throughout the serine recombinase gene phylogenetic tree, and all three genes were oriented in the same direction as the interrupted gene. The xis genes within the Synechococcus sp. PCC 7502 and Cyanothece sp. PCC 7822 elements were located at the beginning of their respective elements, while that of the C. thermalis PCC 7203 hypothetical protein element was the only positively oriented xis gene in this study to be found at the end of the element.
Discussion
Interrupted genes
The newly discovered interruption elements presented here provide context for which to answer many questions that have surrounded these features for decades. Among those orthologs that were not previously reported to contain elements are several genes known to be important to N2 fixation or maintenance of a microoxic microenvironment in heterocysts. The products of nifE and nifB are involved in the synthesis of the nitrogenase Fe/Mo cofactor [41], and hupS encodes an uptake hydrogenase subunit and is in an operon with hupL. nifJ encodes an oxidoreductase that is responsible for electron transfer to nitrogenase, and is required for N2 fixation when iron is limiting [42,43]. A previous study of Nostoc 7120 indicated that expression of genes orthologous to the two element-containing cytochrome c oxidase subunit I copies, coxA2 and coxA3, are specific to heterocysts, while a third copy, coxA1, is expressed only in vegetative cells [44]. The role of cytochrome c oxidase in heterocysts is in respiratory O2 consumption [44]. Similarly, the flv3B gene product of Nostoc 7120 is a heterocyst-specific flavin reductase that reduces O2 [45]. The fatty acid synthase encoded by hglE is involved in the formation of heterocyst glycolipids, which form a layer in the envelope that acts to retard gas diffusion into the heterocyst [46]. Given the heterocyst-specific roles of these genes, the excision of their interruption elements is likely dependent on transcription of the respective xis genes during heterocyst formation, as is assumed to be the case with all of the previously reported elements [15].
The presence of interruption elements within genes with no known role in N2 fixation opens several possibilities. First of all, these interrupted genes may indeed have heterocyst-specific roles and are excised during heterocyst formation. Additionally, the elements may not be excised under any circumstances, thus, leaving the genes that they interrupt non-functional. However, this inactivation would likely lead to rapid deterioration of the interrupted gene, and likely the xis gene, as well. On the other hand, the excision of some elements could be brought on by factors other than heterocyst development, such as differentiation of other cell types. Many heterocyst-forming cyanobacteria also form akinetes [4] and hormogonia [5]. Additionally, the element-containing unicellular Chroococcidiopsis spp. form survival cells upon nitrogen limitation [47]; the excision of the interruption element from the gene encoding a membrane protein could be triggered by the formation of these cells. This idea is supported by a phylogenetic relationship between C. thermalis and heterocyst-forming cyanobacteria that provides a possible evolutionary link between these survival cells and heterocysts [40,48]. Thus, interruption element excision triggered by cell differentiation may be shared between these organisms.
The excision of an interruption element during differentiation of non-heterocyst cell types may require additional mechanisms for the element to persist. Excision of an element during development of a non-terminal cell type, such as hormogonia, akinetes, or the survival cells formed by Chroococcidiopsis spp., would require reintegration into the chromosome upon differentiation back into a vegetative cell. Tn3 family transposases are capable of integrating a donor sequence into a target sequence [24], and Tn3 family transposases are found adjacent to the recombinase genes of the interruption elements within the Calothrix sp. PCC 6303 arabinose efflux permease gene and the C. thermalis PCC 7203 membrane protein. Thus, each is a likely candidate to be excised from the chromosome in a non-terminal manner, and reintegration of these elements could be linked to the reason that the xis genes in these two elements are oriented in different ways than the others in this study. While element excision may be triggered by differentiation of various cell types, the mechanisms could differ depending on the cell type.
Factors other than cell differentiation should also be considered for triggers of interruption element excision in heterocyst-forming cyanobacteria. However, similar to the case of a non-terminal cell type, the excision of interruption elements throughout a population during a single event would result in the element being present in future generations exclusively as extrachromosomal DNA. Reintegration would again be required, but the interruption elements found in Synechococcus sp. PCC 7502 and Cyanothece sp. PCC 7822 do not contain transposases. The presence of interruption elements in these unicellular cyanobacteria, neither of which has been shown to differentiate cells of any kind, supports the possibility of other factors prompting genome rearrangements.
Evolution of recombinase genes and element variants
The two recombinase superfamilies (tyrosine and serine) responsible for interruption element excision from heterocyst-forming cyanobacterial genes are named for the amino acid residue of each that covalently binds to the DNA, and each superfamily uses a different mechanism for recombination [24]. They have different evolutionary histories, and the lack of an evolutionary relationship between the recombinase superfamilies indicates there have been at least two events in which the heterocyst-forming cyanobacterial lineage has acquired interruption elements, one involving each type of recombinase.
The relatedness of the recombinase gene sequences within each superfamily provides clues as to how the interruption elements have evolved in heterocyst-forming cyanobacteria. In general, the recombinase gene sequences mostly clustered with those from the same element variant in other organisms. However, the A. cylindrica PCC 7122 and S. hofmanni UTEX 2349 sets of serine superfamily recombinase gene sequences clustered with others from the same organism, and are likely the result of transposition events within the genome. The Rivularia sp. PCC 7116 xis genes responsible for the nifB and hupS elements are the only examples of tyrosine recombinase gene sequences from the same organism clustering together, and they are much more divergent than those serine recombinase gene clusters. Additionally, serine superfamily recombinase genes are found in elements interrupting more ortholog groups than tyrosine superfamily recombinase genes, including all of the genes with no known N2 fixation role. The relationships of the available recombinase gene sequences provide evidence that serine superfamily recombinase genes have a greater tendency to integrate into a genome or replicon, or replicate within a genome than tyrosine superfamily recombinase genes. This replication is a characteristic of selfish DNA [33], and is likely the mechanism for the origin of an element variant.
The element variant that interrupts nifD at position 1355 (± 2 bp) was, by far, the most common variant observed in the genomes studied here. This was likely either the first interruption element to integrate and persist in heterocyst-forming cyanobacteria, or this particular element variant is more likely to be retained than other elements, possibly due to some advantage it provides to the host organism. Either way, it is this frequently occurring element variant that warrants special attention when examining the origin of interruption elements within this lineage.
Element gene content
Genes present in multiple interruption elements linked some elements together, possibly through their shared origin, such as infecting phages that contained the conserved gene. We were able to identify several genes that were shared amongst elements of a single variant, most commonly the elements that interrupt nifD at position 1355 (± 2 bp), including several that have been previously identified as conserved in many of those elements [18,49,50]. Most of these genes were also found in genomes outside of interruption elements, indicating their functions are likely not element-specific despite their conservation in many elements. The ATPase that was found in six elements is the exception as it was not found in any other genome, although it is unclear what possible function it may have with regards to the element.
The genes encoding translation elongation factor G (TEFG) paralogs in multiple element variants also may have a function specific to the element. TEFG paralogs were found in the Richelia intracellularis HH01 and R. intracellularis RC01 nifH elements, the Calothrix sp. PCC 7103 and Calothrix desertica PCC 7102 nifK elements, and the Rivularia sp. PCC 7116 element that interrupts nifD at position 1353. The C. rhizosoleniae SC01 TEFG paralog is in an 11.9 kb contig, and may be in one of several interruption elements that are disjointed by a contig break (hupL, nifH, nifK, or flv3B) or not in any interruption element. Similarly, the M. testarum BC008 TEFG paralog is located in a 40.5 kb contig. No interruption element has been confirmed in that genome, but there are two possible xis genes that are located near contig edges, and thus, are possible element recombinase genes. Therefore, the TEFG paralog may be exclusively located in interruption elements in heterocyst-forming cyanobacteria. However, the interruption elements containing the TEFG paralogs are not closely related, based on recombinase gene sequences, indicating the TEFG paralog was not simply inherited with that interruption element through speciation. In bacteria, TEFGs are involved in elongation during protein synthesis and ribosome recycling [51–53]. In addition to a TEFG of cyanobacterial ancestry, a TEFG paralog is found in some cyanobacteria [54], including the seven closely related heterocyst-forming strains analyzed here. Thus, the TEFG paralog may be preserved in interruption elements due to an element-specific function, such as a role in the synthesis of proteins encoded in the excised element in the heterocyst.
Based on the relatedness of their recombinase genes, the interruption elements within each variant appear to have a strong evolutionary connection, yet there are very few physical similarities within variant groups. The lack of consistencies in length or GC content among all interruption elements of a single variant indicates that the interruption elements are dynamic sequences that have undergone changes within the individual organisms. The highly variable gene content encoded in each interruption element is also indicative of a dynamic sequence with gene deletions and insertions taking place over time. The transformations that the interruption elements have undergone over time have clouded genetic signatures and made it difficult to connect the elements to their origin.
Conclusion
The extensive analysis reported here provides a framework for which to study interruption elements in cyanobacteria. Given the general lack of conserved gene content in the interruption elements, the recombinase gene sequences provide the best foundation for which to evolutionarily link the elements. A lack of homology between the two recombinase superfamilies implies at least two distinct origins and evolutionary paths of interruption elements in heterocyst-forming cyanobacterial ancestry. However, the relatedness of recombinase gene sequences within each superfamily sheds light on the origin of element variants through recombinase gene replication within a genome, and shows a greater tendency for serine superfamily recombinase genes to undergo this replication. While the previously reported nifD and hupL interruption elements are among the most frequently occurring elements in heterocyst-forming cyanobacteria, our analysis uncovered elements interrupting other gene orthologs, as well as variants of the interruption elements in previous reports. Our discovery of elements that are closely related to elements that have excision triggered by the cell, but interrupt genes that have no known function in N2 fixation, reveals the possibility of factors beyond heterocyst differentiation that could activate the excision of interruption elements. Through expansion of the interruption element data set, we have begun to trace the evolutionary paths of these unique genetic features and identified that their impact is broader than previously thought.
Supporting Information
S1 Data. Calothrix rhizosoleniae SC01 gene sequences.
The DNA sequences for the four xis genes (from Table B in S1 File) and three genes that were shared across elements (from Table C in S1 File) in the Calothrix rhizosoleniae SC01 genome.
https://doi.org/10.1371/journal.pone.0156034.s001
(FAS)
S2 Data. Calothrix rhizosoleniae SC01 contig sequences.
The seven contigs from the Calothrix rhizosoleniae SC01 genome that contained part of an element.
https://doi.org/10.1371/journal.pone.0156034.s002
(FAS)
S1 File. Tables A-C.
Detailed information describing the genomes analyzed in this study, the interruption elements that were found in those genomes, and shared genes across the elements.
https://doi.org/10.1371/journal.pone.0156034.s003
(XLSX)
S2 File. Figures A-H.
Images providing depictions of specific interruption elements, element frequency relative to phylogeny, and element length and GC content trends.
https://doi.org/10.1371/journal.pone.0156034.s004
(PDF)
Acknowledgments
This work was sponsored in part by a Gordon and Betty Moore Foundation Investigator award (#493.01, J.P.Z.) and the NSF Center for Microbial Oceanography: Research and Education (EF0424599, J.P.Z.). We thank I. Shilova and J. Robidart for comments on the manuscript.
Author Contributions
Conceived and designed the experiments: JAH JPZ JCM. Performed the experiments: JAH. Analyzed the data: JAH. Contributed reagents/materials/analysis tools: JPZ. Wrote the paper: JAH JPZ JCM.
References
- 1. Marcus Y, Zenvirth D, Harel E, Kaplan A. Induction of HCO3- transporting capability and high photosynthetic affinity to inorganic carbon by low concentration of CO2 in Anabaena variabilis. Plant Physiol. 1982;69: 1008–1012. pmid:16662334
- 2. Mühling M, Harris N, Belay A, Whitton BA. Reversal of helix orientation in the cyanobacterium Arthrospira. J Phycol. 2003;39: 360–367.
- 3. Pattanaik B, Montgomery BL. FdTonB is involved in the photoregulation of cellular morphology during complementary chromatic adaptation in Fremyella diplosiphon. Microbiology. 2010;156: 731–741. pmid:19959581
- 4.
Kaplan-Levy RN, Hadas O, Summers ML, Rücker J, Sukenik A. Akinetes: dormant cells of cyanobacteria. Dormancy and Resistance in Harsh Environments. New York, NY: Springer; 2010. pp. 5–27.
- 5. Herdman M, Rippka R. Cellular differentiation: hormogonia and baeocytes. Methods Enzymol. 1988;167: 232–242.
- 6.
Wolk CP, Ernst A, Elhai J. Heterocyst metabolism and development. The Molecular Biology of Cyanobacteria. New York, NY: Springer; 2004. pp. 769–823.
- 7. LeBauer DS, Treseder KK. Nitrogen limitation of net primary productivity in terrestrial ecosystems is globally distributed. Ecology. 2008;89: 371–379. pmid:18409427
- 8. Zehr JP, Kudela RM. Nitrogen cycle of the open ocean: from genes to ecosystems. Annu Rev Mar Sci. 2011;3: 197–225.
- 9. Wong PP, Burris RH. Nature of oxygen inhibition of nitrogenase from Azotobacter vinelandii. Proc Natl Acad Sci. 1972;69: 672–675. pmid:4501581
- 10. Zhang C-C, Laurent S, Sakr S, Peng L, Bédu S. Heterocyst differentiation and pattern formation in cyanobacteria: a chorus of signals. Mol Microbiol. 2006;59: 367–375. pmid:16390435
- 11. Christman HD, Campbell EL, Meeks JC. Global transcription profiles of the nitrogen stress response resulting in heterocyst or hormogonium development in Nostoc punctiforme. J Bacteriol. 2011;193: 6874–6886. pmid:22001509
- 12. Ehira S. Transcriptional regulation of heterocyst differentiation in Anabaena sp. strain PCC 7120. Russ J Plant Physiol. 2013;60: 443–452.
- 13. Wang H, Sivonen K, Rouhiainen L, Fewer DP, Lyra C, Rantala-Ylinen A, et al. Genome-derived insights into the biology of the hepatotoxic bloom-forming cyanobacterium Anabaena sp. strain 90. BMC Genomics. 2012;13: 613. pmid:23148582
- 14. Golden JW, Wiest DR. Genome rearrangement and nitrogen fixation in Anabaena blocked by inactivation of xisA gene. Science. 1988;242: 1421–1423. pmid:3144039
- 15. Golden JW, Robinson SJ, Haselkorn R. Rearrangement of nitrogen fixation genes during heterocyst differentiation in the cyanobacterium Anabaena. Nature. 1985;314: 419–423. pmid:3920531
- 16. Carrasco CD, Buettner JA, Golden JW. Programmed DNA rearrangement of a cyanobacterial hupL gene in heterocysts. Proc Natl Acad Sci. 1995;92: 791–795. pmid:7846053
- 17. Carrasco CD, Golden JW. Two heterocyst-specific DNA rearrangements of nif operons in Anabaena cylindrica and Nostoc sp. strain Mac. Microbiology. 1995;141: 2479–2487. pmid:7582007
- 18. Henson BJ, Hartman L, Watson LE, Barnum SR. Evolution and variation of the nifD and hupL elements in the heterocystous cyanobacteria. Int J Syst Evol Microbiol. 2011;61: 2938–2949. pmid:21278412
- 19. Mulligan ME, Haselkorn R. Nitrogen fixation (nif) genes of the cyanobacterium Anabaena species strain PCC 7120. The nifB-fdxN-nifS-nifU operon. J Biol Chem. 1989;264: 19200–19207. pmid:2553733
- 20. Ungerer J, Pratte BS, Thiel T. RNA processing of nitrogenase transcripts in the cyanobacterium Anabaena variabilis. J Bacteriol. 2010;192: 3311–3320. pmid:20435734
- 21. Vintila S, Selao T, Norén A, Bergman B, El-Shehawy R. Characterization of nifH gene expression, modification and rearrangement in Nodularia spumigena strain AV1. FEMS Microbiol Ecol. 2011;77: 449–459. pmid:21569060
- 22. Hilton JA, Foster RA, Tripp HJ, Carter BJ, Zehr JP, Villareal TA. Genomic deletions disrupt nitrogen metabolism pathways of a cyanobacterial diatom symbiont. Nat Commun. 2013;4: 1767. pmid:23612308
- 23. Lammers PJ, Golden JW, Haselkorn R. Identification and sequence of a gene required for a developmentally regulated DNA excision in Anabaena. Cell. 1986;44: 905–911. pmid:3006922
- 24. Carrasco CD, Ramaswamy K, Ramasubramanian T, Golden JW. Anabaena xisF gene encodes a developmentally regulated site-specific recombinase. Genes Dev. 1994;8: 74–83. pmid:8288129
- 25. Carrasco CD, Holliday SD, Hansel A, Lindblad P, Golden JW. Heterocyst-specific excision of the Anabaena sp. strain PCC 7120 hupL element requires xisC. J Bacteriol. 2005;187: 6031–6038. pmid:16109944
- 26. Chastain CJ, Brusca JS, Ramasubramanian TS, Wei T-F, Golden JW. A sequence-specific DNA-binding factor (VF1) from Anabaena sp. strain PCC 7120 vegetative cells binds to three adjacent sites in the xisA upstream region. J Bacteriol. 1990;172: 5044–5051. pmid:2118506
- 27. Ramasubramanian TS, Wei TF, Golden JW. Two Anabaena sp. strain PCC 7120 DNA-binding factors interact with vegetative cell-and heterocyst-specific genes. J Bacteriol. 1994;176: 1214–1223. pmid:8113160
- 28. López-Gomollón S, Hernández JA, Pellicer S, Angarica VE, Peleato ML, Fillat MF. Cross-talk between iron and nitrogen regulatory networks in Anabaena (Nostoc) sp. PCC 7120: identification of overlapping genes in FurA and NtcA regulons. J Mol Biol. 2007;374: 267–281. pmid:17920076
- 29. Ramaswamy K, Carrasco CD, Fatma T, Golden JW. Cell-type specificity of the Anabaena fdxN-element rearrangement requires xisH and xisI. Mol Microbiol. 1997;23: 1241–1249. pmid:9106215
- 30. Hwang WC, Golden JW, Pascual J, Xu D, Cheltsov A, Godzik A. Site-specific recombination of nitrogen-fixation genes in cyanobacteria by XisF-XisH-XisI complex: structures and models. Proteins Struct Funct Bioinforma.
- 31. Haselkorn R. Developmentally regulated gene rearrangements in prokaryotes. Annu Rev Genet. 1992;26: 113–130. pmid:1482108
- 32. Orgel LE, Crick FHC, Sapienza C. Selfish DNA. Nature. 1980;288: 645–646. pmid:7453798
- 33. Brusca JS, Chastain CJ, Golden JW. Expression of the Anabaena sp. strain PCC 7120 xisA gene from a heterologous promoter results in excision of the nifD element. J Bacteriol. 1990;172: 3925–3931. pmid:2113913
- 34. Meeks JC, Campbell EL, Bisen PS. Elements interrupting nitrogen fixation genes in cyanobacteria: presence and absence of a nifD element in clones of Nostoc sp. strain Mac. Microbiology. 1994;140: 3225–3232.
- 35. Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994;22: 4673–4680. pmid:7984417
- 36. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011;28: 2731–2739. pmid:21546353
- 37. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution. 1985;39: 783–791.
- 38. Shih PM, Wu D, Latifi A, Axen SD, Fewer DP, Talla E, et al. Improving the coverage of the cyanobacterial phylum using diversity-driven genome sequencing. Proc Natl Acad Sci. 2013;110: 1053–1058. pmid:23277585
- 39. Howard-Azzeh M, Shamseer L, Schellhorn HE, Gupta RS. Phylogenetic analysis and molecular signatures defining a monophyletic clade of heterocystous cyanobacteria and identifying its closest relative. Photosynth Res. 2014;122: 171–185. pmid:24917519
- 40. Roberts GP, MacNeil T, MacNeil D, Brill WJ. Regulation and characterization of protein products coded by the nif (nitrogen fixation) genes of Klebsiella pneumoniae. J Bacteriol. 1978;136: 267–279. pmid:361694
- 41. Shah VK, Stacey G, Brill WJ. Electron transport to nitrogenase. Purification and characterization of pyruvate: flavodoxin oxidoreductase. The nifJ gene product. J Biol Chem. 1983;258: 12064–12068. pmid:6352705
- 42. Bauer CC, Scappino L, Haselkorn R. Growth of the cyanobacterium Anabaena on molecular nitrogen: NifJ is required when iron is limited. Proc Natl Acad Sci. 1993;90: 8812–8816. pmid:8415612
- 43. Valladares A, Herrero A, Pils D, Schmetterer G, Flores E. Cytochrome c oxidase genes required for nitrogenase activity and diazotrophic growth in Anabaena sp. PCC 7120. Mol Microbiol. 2003;47: 1239–1249. pmid:12603731
- 44. Ermakova M, Battchikova N, Allahverdiyeva Y, Aro E-M. Novel heterocyst-specific flavodiiron proteins in Anabaena sp. PCC 7120. FEBS Lett. 2013;587: 82–87. pmid:23178714
- 45. Campbell EL, Cohen MF, Meeks JC. A polyketide-synthase-like gene is involved in the synthesis of heterocyst glycolipids in Nostoc punctiforme strain ATCC 29133. Arch Microbiol. 1997;167: 251–258. pmid:9075624
- 46. Billi D, Grilli-Caiola M. Effects of nitrogen limitation and starvation on Chroococcidiopsis sp. (Chroococcales). New Phytol. 1996;133: 563–571.
- 47. Fewer D, Friedl T, Büdel B. Chroococcidiopsis and heterocyst-differentiating cyanobacteria are each other’s closest living relatives. Mol Phylogenet Evol. 2002;23: 82–90. pmid:12182405
- 48. Grindley ND, Whiteson KL, Rice PA. Mechanisms of site-specific recombination. Annu Rev Biochem. 2006;75: 567–605. pmid:16756503
- 49. Lammers PJ, McLaughlin S, Papin S, Trujillo-Provencio C, Ryncarz AJ. Developmental rearrangement of cyanobacterial nif genes: nucleotide sequence, open reading frames, and cytochrome P-450 homology of the Anabaena sp. strain PCC 7120 nifD element. J Bacteriol. 1990;172: 6981–6990. pmid:2123860
- 50. Henson BJ, Watson LE, Barnum SR. Characterization of a 4 kb variant of the nifD element in Anabaena sp. strain ATCC 33047. Curr Microbiol. 2005;50: 129–132. pmid:15883871
- 51. Rodnina MV, Savelsbergh A, Katunin VI, Wintermeyer W. Hydrolysis of GTP by elongation factor G drives tRNA movement on the ribosome. Nature. 1997;385: 37–41. pmid:8985244
- 52. Hirokawa G, Nijman RM, Raj VS, Kaji H, Igarashi K, Kaji A. The role of ribosome recycling factor in dissociation of 70S ribosomes into subunits. RNA. 2005;11: 1317–1328. pmid:16043510
- 53. Zavialov AV, Hauryliuk VV, Ehrenberg M. Splitting of the posttermination ribosome into subunits by the concerted action of RRF and EF-G. Mol Cell. 2005;18: 675–686. pmid:15949442
- 54. Atkinson GC, Baldauf SL. Evolution of elongation factor G and the origins of mitochondrial and chloroplast forms. Mol Biol Evol. 2011;28: 1281–1292. pmid:21097998