Correction
12 Mar 2015: The PLOS ONE Staff (2015) Correction: Sperm Morphology in Two House Mouse Subspecies: Do Wild-Derived Strains and Wild Mice Tell the Same Story?. PLOS ONE 10(3): e0120484. https://doi.org/10.1371/journal.pone.0120484 View correction
Figures
Abstract
Being subject to intense post-copulatory selection, sperm size is a principal determining component of male fitness. Although previous studies have presented comparative sperm size data at higher taxonomic levels, information on the evolution of sperm size within species is generally lacking. Here, we studied two house mouse subspecies, Mus musculus musculus and Mus musculus domesticus, which undergo incipient speciation. We measured four sperm dimensions from cauda epididymis smears of 28 wild-caught mice of both subspecies. As inbred mouse strains are frequently used as proxies for exploring evolutionary processes, we further studied four wild-derived inbred strains from each subspecies. The subspecies differed significantly in terms of sperm head length and midpiece length, and these differences were consistent for wild mice and wild-derived strains pooled over genomes. When the inbred strains were analyzed individually, however, their strain-specific values were in some cases significantly shifted from subspecies-specific values derived from wild mice. We conclude that: (1) the size of sperm components differ in the two house mouse subspecies studied, and that (2) wild-derived strains reflect this natural polymorphism, serving as a potential tool to identify the genetic variation driving these evolutionary processes. Nevertheless, we suggest that more strains should be used in future experiments to account for natural variation and to avoid confounding results due to reduced variability and/or founder effect in the individual strains.
Citation: Albrechtová J, Albrecht T, Ďureje L, Pallazola VA, Piálek J (2014) Sperm Morphology in Two House Mouse Subspecies: Do Wild-Derived Strains and Wild Mice Tell the Same Story? PLoS ONE 9(12): e115669. https://doi.org/10.1371/journal.pone.0115669
Editor: Norman Johnson, University of Massachusetts, United States of America
Received: August 14, 2014; Accepted: November 28, 2014; Published: December 26, 2014
Copyright: © 2014 Albrechtová 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: The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper and its Supporting Information files.
Funding: Research was supported by the Czech Science Foundation (206-08-0640) (JP), and the National Science Foundation (DEB0746560) (VAP). The funders had no role in study design, data collection, data analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
In promiscuous species, sperm size, as determined by male-male sperm competition and cryptic female choice [1]-[3], is a principal component of male fitness. Comparative data between more distantly related species (typically involving single or a few individuals per species) reveal variation in sperm size reaching up to three orders of magnitude among animal taxa and over 12-fold in mammals [4]-[10]. At the opposite end of the evolutionary spectrum, population-based studies focused on single species have found that higher levels of promiscuity are associated with longer sperm and decreased sperm size variation among males [11]-[13]. The house mouse represents a suitable model for studying sperm size evolution in a taxon at an intermediate level of divergence. Two house mouse subspecies, Mus musculus musculus (Mmm) and Mus musculus domesticus (Mmd), diverged about 350,000 years ago [14] and colonized Europe with the spread of agriculture [15]. In regions where their populations abut, these subspecies form a long, narrow secondary hybrid zone stretching from Norway to the Black Sea [16], [17]. For most of their divergence time, the two species' ranges were separated, allowing them to accumulate numerous genetic incompatibilities [18]. Recent studies have suggested that traits related to sperm quality and function, namely sperm number and sperm velocity, may be implicated in the maintenance of the house mouse hybrid zone (HMHZ) [19], [20]. Identification of spermatogenesis as a male fitness component with rapidly evolving incompatibilities led us to ask whether sperm size differentiation occurred simultaneous to mouse subspecific divergence.
Previous intrasubspecific studies relied on the presence of a variety of classical laboratory inbred strains (CLS) with a long-standing history of inbreeding, maintaining characteristic individual phenotypes [21]. Comparison of various classical strains revealed substantial strain-specific variation in sperm head dimension and in the incidence of head abnormalities; the inter-strain variation observed is explained by genetic differences among these traits - e.g. [22]-[24]. The observed sperm size differentiation is, however, difficult to extrapolate into an evolutionary pattern, as the classical strains are mixtures of three mouse genomes with limited, non-randomly distributed haplotype diversity [25].
To avoid the confounding factors mentioned above, wild-derived strains (WDS) can be a suitable substitution for CLS in understanding the evolutionary forces that shape sperm size. For example, Firman and Simmons (2010) [26] studied selection lines derived from WDS of Mmd (Mmd-WDS) and identified substantial, intrasubspecific variation in sperm midpiece length. This may suggest that variation also exists in natural populations. Although sperm size may be a key predictor for fertilization success in promiscuous species such as mice [26]-[29], only Mmd-WDS have been studied previously, and studies on wild mice in this context have not yet been published.
In this study, we measured four sperm components in wild mice and WDS from European allopatric populations that represent both house mouse subspecies. We focused on the (i) detection of intersubspecific differences in sperm size components and (ii) comparison of sperm phenotypic variability of wild-derived strains and wild individuals. Specifically, by decomposing phenotypic variation within and between compared groups, we aimed to determine whether WDS might be utilized to study the genetic basis of intra- and intersubspecific sperm differentiation, and furthermore to model evolutionary processes that affect sperm phenotypes.
Materials and Methods
Wild mice from both Mmm (N = 28) and Mmd (N = 28) subspecies were live-trapped in several European allopatric populations from 2005 – 2011 (see Table 1 for their position). The subspecific origin of each male was based on geographic position of the locality relative to the position of the house mouse hybrid zone [16]. To confirm subspecific status, DNA was isolated from alcohol-preserved spleens and analyzed for the presence of diagnostic alleles at eight markers. The primers and PCR conditions for individual loci followed the protocol described earlier: BamH I restriction site in the Nd1 gene in mtDNA [30]; 18-bp deletion within the Y-linked Zink finger protein 2 gene (Zfy2) [31]; SINE B1 insertion in the Bruton agammaglobulinemia tyrosine kinase gene (Btk) and Tsx on the X chromosome [31], [32]; SINE B2 insertion 3′ downstream the Syap1 gene [33]; LINE1 insertion XL1_332L07 (X332), the SINE B2 insertion XB2_347N11 (X347), and X65 [34]. According to NCBI Build 38 (http://www.ncbi.nlm.nih.gov/), physical positions of the X-linked markers are: 17.13, 51.79, 73.77, 103.41, 135.54 and 161.57 Mb for X332, X347, X65, Tsx, Btk and Syap1, respectively.
Ten males of eight WDS representing Mmd (SCHEST, SIT, STRA, STRB) and Mmm (BUSNA, PWD/Ph, STUS, STUF) subspecies were studied. STRA, STRB and BUSNA strains were derived from wild populations 50 km east or west of the approximated hybrid zone center at their given latitudes [35]. STUS, STUF and PWD/Ph mice came from allopatric Mmm populations in the Czech Republic [35], [36]. All these strains were fully inbred (i.e. more than 20 generations of brother-sister mating) at the time of the study. The ancestors of the SCHEST strain were caught in Central Germany (Schweben, Hessen: [N: 50° 26′, E: 9° 35′]) in 2007. A parental pair of the SIT strain was sampled at Scar, Whitemill Bay, Sanday Island (Orkneys, Scotland [N: 59° 18′, E: -2° 33′]) in 2006. These two strains had undergone 4-10 and 4-9 generations of inbreeding, respectively, at the time of the study. Subspecific affiliations of the BUSNA, PWD, STRA, STRB, STUS and STUF strains were known a priori [35], [36]. The SCHEST and SIT mice were analyzed for the same eight diagnostic loci and were found to carry Mmd alleles (Table 1).
The animals were kept at the barrier-free facility of the Institute of Vertebrate Biology in Studenec and their care was in accordance with the standards set by the Czech Republic Act for Experimental Work, with animals fully compatible with corresponding regulations and standards of the European Union (license 227203/2011-MZE-17214). The experimental protocol was approved by the Committee on the Ethics of Animal Experiments of the Institute of Vertebrate Biology (Permit Number 27/2007). All mice were kept in polypropylene cages with bedding material under standard conditions: 20-22°C, 14/10-hr light/dark cycle. Tap-water and mouse pelleted food (St1, VELAZ, Prague, Czech Republic) were available ad libitum. Male mice were housed either individually or in pairs with a female of the same strain, and were sacrificed when age reached at least 60 days (Table 2). The paired males were separated for a minimum of five days to be kept in single cages preceding sacrifice and sperm collection.
The study protocol did not allow for absolute age to be completely controlled. The absolute age of caught wild mice was unknown. Additionally, individuals were kept in captivity for varying numbers of days before sacrifice (Table 2). We tried to control for the second limitation by choosing wild males for comparison that had, on average (mean 179 days, F7,72 = 0.32, P = 0.94), spent the same amount of time in captivity. Contrary to wild mice, the age of WDS males was known. Two criteria for choosing experimental males were applied: only males aged more than 60 days were scored, and males were selected to have, on average, the same age between the Mmd and Mmm groups. After dislocation, left cauda epididymides were dissected and transferred into the medium (DMEM, Invitrogen, Germany), heated to 37°C, and punctured by needles that released sperm into the medium. Sperm were allowed to swim freely for five minutes. A drop of sperm suspension was smeared on a slide, air-dried, and fixed in 5% Giemsa solution (Sigma-Aldrich, Germany) for 15 min.
Images of sperm were captured via microscopy (BX51, Olympus, Czech Republic) and digital camera (DP71, Olympus) at 400× magnification. Four sperm dimensions: head length, head width, midpiece length, and tail length (Fig. 1) were measured with Olympus imaging software (QuickPHOTO Industrial 2.3, Olympus). Ten sperm were measured per individual. The measurement accuracy was to one tenth of a micrometer (µm). For statistical analysis, one-way ANOVA on sample means was performed. We used the dataset for three separate tests (wild Mmd vs. wild Mmm; wild vs. individual WDS; wild vs. subspecies-specific WDS grouped together). Consequently, Bonferroni adjustments were applied to correct for multiple comparisons and omnibus test type I error was set to α = 0.05/3. When significant differences between groups were detected, Tukey post-hoc contrast analysis was employed to specify among-group differences.
Measures of sperm midpiece length and tail length are highlighted in yellow and red. Sperm head length and width measurements are represented by dashed lines.
To quantify the reliability of WDS as a surrogate for sperm size variation in wild mice, linear discriminant analysis was applied as implemented in the MASS package of R environment (http://cran.r-project.org). Cross-validated discriminant scores were calculated for significantly different sperm size variables (sperm head length, sperm head width, and midpiece length) separately for wild and WDS mice. Success of classification of mice into Mmd or Mmm as predicted by discriminant function was compared to subspecific origin as assessed by genetic analysis.
Results
Molecular analyses of six diagnostic markers separated wild mice into two genetically distinct groups (Table 1). Genotypes were mostly in accordance with expected geographic position of Mmd and Mmm subspecies [16], [17]. One exception was an individual mouse from a locality in Western Austria (Silz: 47°15′ N/10°55′ E) that carried Mmm alleles. Consequently, this individual was treated as Mmm in further analyses.
The sperm component measurements of wild individuals are available in S1 Table. The wild Mmd and Mmm groups differed in terms of midpiece length (F1,54 = 48.54, P<0.001), sperm head length (F1,54 = 38.15, P<0.001), and head width (F1,54 = 6.52, P = 0.01); in all cases, values were higher in Mmm as compared to Mmd (Fig. 2, Table 2). Given that Mmd and Mmm differed in two sperm length components, it is not surprising that these two groups also differed in total sperm length (F1,54 = 6.67, P = 0.01). The only non-significant variable reported was sperm tail length (F1,54 = 0.21, P = 0.65).
Sperm head length (A), sperm head width (B), midpiece length (C), and tail length (D). Individual wild-derived strains are marked separately on the left side of the graphs while subspecies-specific strains are put together on the right side of the graphs. The same upper-case letters indicate similarity of sperm components between subspecies and strains in the Tukey post hoc test comparison. Error bars represent 95% confidence intervals.
A scatterplot of wild mice in a reduced morphospace defined by the two most statistically significant variables revealed only marginal mixing of the two groups (1 Mmm within Mmd and 2 Mmd within Mmm in Fig. 3). Discriminant analysis based on three significantly different variables (sperm head length, sperm head width, and midpiece length) assigned 52 out of 56 (92.9%) wild mice correctly to their respective genetic backgrounds (Table 3).
Mmd-specific mice are shown in blue and Mmm-specific mice in red.
The subspecies-attributed sperm size differentiation showed a similar pattern when WDS mice that were grouped according to subspecies were added to morphometric analysis (Fig. 2). Tukey post-hoc contrast clearly separated Mmm and Mmd mice at midpiece length (F3,132 = 46.50, P<0.001) and sperm head length (F3,132 = 16.58, P<0.001). The subspecific partitioning of phenotypic variability was less clear in the remaining variables. Although the four groups differed in terms of sperm head width (F3,132 = 9.82, P<0.001), only Mmm-WDS had significantly wider sperm heads (Fig. 2, S2 Table). Similarly, differentiation was observed in terms of sperm tail length (F3,132 = 13.85, P<0.001), but this could be attributed to Mmd-WDS having longer tails, on average (Fig. 2, S2 Table). The differences were also found in the total sperm length (F3,132 = 9.77, P<0.001). Tukey post-hoc contrast separated wild Mmd possessing shorter sperm from the other three groups of mice (mean±standard deviation, 124.26±1.70 µm for wild Mmd compared to 126.82±2.01 µm representing average for wild and Mmm-WDS and Mmd-WDS). Discriminant analysis utilizing the same three length measures as mentioned in the previous paragraph performed slightly worse when all mice were analyzed. The summed value of correct assignments of wild and inbred mice was 120/136 (88.2%) with respect to their Mmd and Mmm genotypes (Table 3).
When individual strains were compared separately, variation in most traits could be partitioned into more detailed differentiation. Significant differentiation was found in all sperm variables (maximum F9,126 = 36.33 for midpiece, minimum F9,126 = 6.83 for total sperm length; P<0.001 for all traits). While the post-hoc tests of mice grouped over subspecies divided variation into two levels mostly corresponding to Mmd and Mmm, up to five different levels were discerned by Tukey post-hoc contrast analysis (cf. left and right panels in Fig. 2; all pairwise comparisons are listed in S2 Table). Individual WDS did differ in terms of sperm size not only between, but also within the same subspecies. In some WDS, sperm size components moved from subspecies-specific values. This pattern can be exemplified by the STUF (Mmm) males who have sperm head lengths similar to that of the average Mmd mouse (Figs. 2 and 3, Table 2). The direction of the intersubspecific shifts was not always predictable for all sperm traits. For example, SCHEST (Mmd) males had midpiece lengths lower than wild Mmd but were indistinguishable from any group of Mmm males in terms of sperm head width (Fig. 2).
Discussion
An important finding of this study was that Mmm and Mmd house mouse subspecies substantially differed in terms of certain sperm size components. Despite the presence of geographic variation in sperm size documented in wild mice (Table 1, Fig. 3), spermatozoa of wild Mmm were characterized by significantly larger head and midpiece length than spermatozoa of Mmd (Fig. 2).
Breeding conditions of all individuals were standardized, and therefore cannot be responsible for the observed variation in sperm traits. Similarly, although males were sacrificed at different ages, or days spent in captivity (see Table 2 for ranges), we controlled for this effect by choosing WDS males that have the same age when processed. Additionally, previous research has demonstrated that there are no age-specific effects on head area and midpiece length in laboratory mouse spermatozoa [37].
Although there is a strong phylogenetic component that influences sperm morphology [9], [38], it is unlikely to be the primary explanatory factor for the differences seen in this study. The two house mouse subspecies started to diverge roughly 350,000 years ago [14], currently forming a monophyletic clade within the genus Mus [39], [40]. To explain factors shaping sperm size evolution, one would have to further explore differences in mating systems and sexual selection within these mouse lineages. Promiscuity and male-male sperm competition in female's reproductive tract is a result of post-copulatory sexual selection [9], [41], which causes variance in morphology of sperm [38]. Sperm morphology influences other sperm traits such as sperm velocity (e.g. in primates [42], birds [12], and mice [26]), and is ultimately one of the main indicators of a male's success when sperm competition occurs [2], [3]. However, some controversy holds on this subject as no such associations were reported to be likely in red deer or in mice [20], [43].
Promiscuity has evolved in both subspecies. Multiple paternity was reported to range between 23-30% in Mmd [28], [29], [44] and 29% in Mmm [45], and is not sufficient to explain the differences observed in sperm size between the mouse subspecies. Previous studies have reported that Mmm and Mmd subspecies differ in terms of sperm velocity, with velocity being higher in Mmm than Mmd [20], [46]. Analysis of 180 males sampled directly from the HMHZ, however, did not reveal significant differences in sperm motility between the subspecies [19]. Wild males of Mmm were shown to display lower sperm counts than their Mmd counterparts [19]. The larger sperm size can indicate a trade-off between sperm number and size in different taxa, e.g. [47]. However, there is no evidence to suggest trade-offs between sperm traits in muroid species [48].
Studies inferring selection and genetic basis of sperm size differences may benefit from including natural variation found regularly in wild animal specimens. One focus of the current study was to assess the reliability of wild-derived strains as proxies for processes occurring in the wild. Analysis of within-subspecies groups of WDS and their wild conspecifics showed consistent patterns in two morphometric variables (cf. sperm head and midpiece lengths in Fig. 2). This finding is promising as it gives support to WDS as a suitable model for studies on sperm size evolution of the house mouse. However, closer inspection has revealed differences in sperm morphology between particular strains of both Mmd and Mmm. For example, STUF (Mmm) spermatozoa have shorter heads than other Mmm individuals. Under post hoc comparison, these spermatozoa are clustered with wild Mmd and three Mmd-WDS: SCHEST, STRB, and SIT (Fig. 2, Table 2). Similarly, the STRA (Mmd) males were outliers within Mmd, having sperm head width similar to Mmm mice (Fig. 2, Table 2). In any case, the next logical step should be to determine which factors cause these strain-specific differences.
The most obvious explanation for strain-specific differences in sperm dimension lies in the very process of WDS derivation. Usually, a single (randomly chosen) individual can be selected as progenitor of the strain, and may inevitably preserve only limited genetic variation of a natural population. Given that there is a heritable component of sperm design [23], [49]-[51], sons will most likely display sperm traits similar to their father. Consequently, individual WDS mice will only present a snap-shot of phenotypic variation depending on the values of the progenitor pair selected to form the WDS. This possibility is exemplified in Fig. 3, which shows phenotypic variation in sperm head length and midpiece length. Although both variables are significantly larger in Mmm than in Mmd (Fig. 2, Table 2), high phenotypic variation was detected at subspecific levels. Values of wild mice and WDS from both subspecies were partly overlapping. The most probable explanation for the distribution of STUF, STUS and SIT males within the morphospace seems to be due to a lineage stemming from ancestral parents with extraordinary phenotypes. Alternative explanations may lie in mouse divergence and/or colonization history. House mouse genomes have a large degree of incomplete lineage sorting [52]-[54]. Therefore, these phenotypes could reflect ancestral polymorphisms for sperm traits still segregating among the subspecies. Additional sampling will be necessary among wild-caught subspecies to determine how extraordinary these phenotypes are.
Strain-specific sperm dimensions may additionally be viewed from a second perspective. WDS with extreme sperm component values are potentially suitable sources for quantitative trait loci (QTL) mapping from F2 or a backcrossed offspring. Distribution of individual mice in Fig. 3 reveals the presence of a paired WDS lying at the opposite edge of morphospace. Consequently, both intrasubspecific crosses (i.e. crosses that would avoid negative interaction between incompatible loci, such as BUSNA x STUF in Mmm) or intersubspecific crosses (i.e. those seeing for effects of hybridization like PWD x STRB) may be implemented to map QTL of sperm size.
The genetic analysis of wild mice broadens our understanding of the two house mouse subspecies borders. The finding of an individual that carries both mitochondrial and sex-linked traits of Mmm genome in a region where the presence of Mmd mice was expected [17] is rather surprising. Nevertheless, these data are in agreement with a recent report of a mouse from a neighboring village in Tyrol (Staudach: 47°16′ N/10°57′ E; 2.5 km apart from previous locality) that carries mtDNA of Mmm origin [55]. These findings of two independent Mmm samples far westward of the house mouse hybrid zone in the Alpine valley of the Inn River may indicate the presence of another, undescribed stretch of subspecies contact. However, we cannot exclude the possibility that this unexpected finding of two Mmm samples is the result of long-distance human-mediated migration.
Supporting Information
S1 Table.
Mean values of sperm dimensions (in µm) per sperm sample and standard deviation (±SD) of wild house mice.
https://doi.org/10.1371/journal.pone.0115669.s001
(PDF)
S2 Table.
Post-hoc comparisons of differences in selected sperm traits between wild Mmd (MmdW), wild Mmm (MmmW) and wild-derived strains (WDS). Shown are results of Tukey post-hoc tests for comparisons of MmdW, MmmW and either WDS grouped (MmdWDS for M. m. domesticus strains and MmmWDS for M. m. musculus strains, panels A-E) or WDS treated separately (Mmm-WDS: BUSNA, PWD, STUS, STUF; Mmd-WDS: SCHEST, STRB, SIT, STRA, panels F-J). (Padj - P value adjusted for multiple comparisons).
https://doi.org/10.1371/journal.pone.0115669.s002
(PDF)
Acknowledgments
We thank Natália Martínková, Stanislav Martínek and Jeremy B. Searle who collected wild mice in Orkneys and Dagmar Čížková, Věra Konečná, and Adam Konečný for providing mice from Central Germany. Dana Havelková, Jana Piálková, and Helena Hejlová are also thanked for their help with strain maintenance and development. Finally, Lucie Vlčková is thanked for help with mouse genotyping.
Author Contributions
Conceived and designed the experiments: JA JP. Performed the experiments: JA JP LĎ. Analyzed the data: JA JP TA. Contributed reagents/materials/analysis tools: JP. Wrote the paper: JA TA VAP JP.
References
- 1.
Eberhard WG (1996) Female Control: Sexual Selection by Cryptic Female Choice. Princeton University Press, Princeton.
- 2.
Birkhead TR, Møller AP (1998) Sperm Competition and Sexual Selection. London: Academic Press.
- 3.
Birkhead TR, Hosken DJ, Pitnick S, eds (2009) Sperm Biology, an Evolutionary Perspective (Elsevier, London).
- 4. Cummins JM, Woodall PF (1985) On mammalian sperm dimensions. Journal of Reproduction and Fertility 75:153–175.
- 5. Gage MJG (1998) Mammalian sperm morphometry. Proceedings of the Royal Society London B 265:97–103.
- 6.
Pitnick S, Hosken DJ, Birkhead TR (2009) Sperm morphological diversity. In Birkhead TR, Hosken DJ, Pitnick S, editors. Sperm biology: an evolutionary perspective. Oxford, UK: Academic Press, pp.69–149.
- 7. Lüpold S, Calhim S, Immler S, Birkhead TR (2009) Sperm morphology and sperm velocity in passerine birds. Proceedings of the Royal Society London B 276:1175–1181.
- 8. Montoto LG, Sánchez MV, Tourmente M, Martín-Coello J, Luque-Larena JJ, et al. (2011b) Sperm competition differentially affects swimming velocity and size of spermatozoa from closely related muroid rodents: head first. Reproduction 142:819–830.
- 9. Higginson DM, Miller KB, Segraves KA, Pitnick S (2012) Female reproductive tract form drives the evolution of complex sperm morphology. Proceedings of the National Academy of Sciences of the United States of America 109:4538–4543.
- 10. Immler S, Gonzalez-Voyer A, Birkhead TR (2012a) Distinct evolutionary patterns of morphometric sperm traits in passerine birds. Proceedings of the Royal Society London B 279:4174–4182.
- 11. Ward PI (1998) Intraspecific variation in sperm size characters. Heredity 80:55–659.
- 12. Laskemoen T, Kleven O, Fossoy F, Robertson RJ, Rudolfsen G, et al. (2010) Sperm quantity and quality effects on fertilization success in a highly promiscuous passerine, the tree swallow Tachycineta bicolor. Behavioral Ecology and Sociobiology 64:1473–1483.
- 13. Laskemoen T, Albrecht A, Bonisoli-Alquati A, Cepák J, de Lope F, et al. (2013) Variation in sperm morphometry and sperm competition among barn swallow (Hirundo rustica) populations. Behavioral Ecology and Sociobiology 67:301–309.
- 14. Geraldes A, Basset P, Smith KL, Nachman MW (2011) Higher differentiation among subspecies of the house mouse (Mus musculus) in genomic regions with low recombination. Molecular Ecology 20:4722–4736.
- 15.
Cucchi T, Auffray JC, Vigne JD (2012) On the origin of the house mouse synanthropy and dispersal in the Near East and Europe: zooarchaeological review and perspectives. In Macholán M, Baird SJE, Munclinger P, Piálek J, editors. Evolution of the House Mouse. Cambridge, UK: Cambridge University Press, pp.65–93.
- 16.
Baird SJE, Macholán M (2012) What can the Mus musculus musculus/M. m. domesticus hybrid zone tell us about speciation? In Macholán M, Baird SJE, Munclinger P, Piálek J editors. Evolution of the House Mouse. Cambridge, UK: Cambridge University Press, pp.334–372.
- 17. Ďureje L, Macholán M, Baird SJE, Piálek J (2012) The mouse hybrid zone in Central Europe: from morphology to molecules. Folia Zoologica 61:308–318.
- 18. Duvaux L, Belkhir K, Boulesteix M, Boursot P (2011) Isolation and gene flow: inferring the speciation history of European house mice. Molecular Ecology 20:5248–5264.
- 19. Albrechtová J, Albrecht T, Baird SJE, Macholán M, Rudolfsen G, et al. (2012) Sperm-related phenotypes implicated in both maintenance and breakdown of a natural species barrier in the house mouse. Proceedings of the Royal Society London B 279:4803–4810.
- 20. Turner LM, Schwahn DJ, Harr B (2012) Reduced male fertility is common but highly variable in form and severity in a natural house mouse hybrid zone. Evolution 66:443–458.
- 21.
Festing MFV (1996) Origins and characteristics of inbred strains of mice. In: Lyon MF, Rastan S, Brown SDM, editors. Genetic Variants and Strains of the Laboratory Mousev Oxford: Oxford University Press. pp.1577–1596.
- 22. Braden AWH (1959) Strain differences in the morphology of the gametes of the mouse. Australian Journal of Biological Sciences 12:65–71.
- 23. Illisson L (1969) Spermatozoal head shape in two inbred strains of mice and their F1 and F2 progenies. Australian Journal of Biological Sciences 22:947–963.
- 24. Osadchuk L, Osadchuk A (2010) Genetic variability of spermatozoon production and morphology in laboratory mice. Bulletin of Experimental Biology and Medicine 149:739–742.
- 25. Yang HN, Wang JR, Didion JP, Buus RJ, Bell TA, et al. (2011) Subspecific origin and haplotype diversity in the laboratory mouse. Nature Genetics 43:648–655.
- 26. Firman RC, Simmons LW (2010) Sperm midpiece length predicts sperm swimming velocity in house mice. Biology Letters 6:513–516.
- 27. Rolland C, MacDonald DW, De Fraipont M, Berdoy M (2003) Free female choice in house mice: Leaving best for last. Behaviour 140:1371–1388.
- 28. Dean MD, Ardlie KG, Nachman MW (2006) The frequency of multiple paternity suggests that sperm competition is common in house mice (Mus domesticus). Molecular Ecology 15:4141–4151.
- 29. Firman RC, Simmons LW (2008) The frequency of multiple paternity predicts variation in testes size among island populations of house mice. Journal of Evolutionary Biology 21:1524–1533.
- 30. Božíková E, Munclinger P, Teeter C, Tucker PK, Macholán M, et al. (2005) Mitochondrial DNA in the hybrid zone between Mus musculus musculus and Mus musculus domesticus: a comparison of two transects. Biological Journal of the Linnean Society 84:363–378.
- 31. Munclinger P, Božíková E, Šugerková M, Piálek J, Macholán M (2002) Genetic variation in house mice (Mus, muridae, rodentia) from the Czech and Slovak republics. Folia Zoologica 51:81–92.
- 32. Munclinger P, Boursot P, Dod B (2003) B1 insertions as easy markers for mouse population studies. Mammalian Genome 14:359–366.
- 33. Macholán M, Munclinger P, Šugerková M, Dufková P, Bímová B, et al. (2007) Genetic analysis of autosomal and X-linked markers across a mouse hybrid zone. Evolution 61:746–771.
- 34. Macholán M, Baird SJE, Dufková P, Munclinger P, Vošlajerová Bímová B, et al. (2011) Assessing multilocus introgression patterns: a case study on the mouse X chromosome in Central Europe. Evolution 65:1428–1446.
- 35. Piálek J, Vyskočilová M, Bímová B, Havelková D, Piálková J, et al. (2008) Development of unique house mouse resources suitable for evolutionary studies of speciation. Journal of Heredity 99:34–44.
- 36. Gregorová S, Forejt J (2000) PWD/Ph and PWK/Ph inbred mouse strains of Mus m. musculus subspecies—a valuable resource of phenotypic variations and genomic polymorphisms. Folia Biologica 46:31–41.
- 37. Beatty RA, Mukherje DP (1963) Spermatozoan characteristics in mice of different ages. Journal of Reproduction and Fertility 6:261–268.
- 38. Kleven O, Laskemoen T, Fossoy F, Robertson RJ, Lifjeld JT (2008) Intraspecific variation in sperm length is negatively related to sperm competition in passerine birds. Evolution 62:494–499.
- 39. Lundrigan BL, Jansa SA, Tucker PK (2002) Phylogenetic relationships in the genus Mus, based on paternally, maternally, and biparentally inherited characters. Systematic Biology 51:410–431.
- 40.
Suzuki H, Aplin KP (2012) Phylogeny and biogeography of the genus Mus in Eurasia. In Macholán M, Baird SJE, Munclinger P, Piálek J editors. Evolution of the House Mouse. Cambridge, UK: Cambridge University Press, pp.35–64.
- 41. Birkhead TR (2010) How stupid not to have thought of that: postcopulatory sexual selection. J Zool 281:78–93.
- 42. Anderson MJ, Dixson AF (2002) Motility and the midpiece in primates. Nature 416:496.
- 43. Malo AF, Gomendio M, Garde J, Lang-Lenton B, Soler AJ, et al. (2006) Sperm design and sperm function. Biol Lett 2:246–249.
- 44. Manser A, Lindholm AK, König B, Bagheri HC (2011) Polyandry and the decrease of a selfish genetic element in a wild house mouse population. Evolution 65:2435–2447.
- 45. Thonhauser KE, Thoss M, Musolf K, Klaus T, Penn DJ (2014) Multiple paternity in wild house mice (Mus musculus musculus): effects on offspring genetic diversity and body mass. Ecology and Evolution 4:200–209.
- 46. Dean MD, Nachman MW (2009) Faster fertilization rate in conspecific versus heterospecific matings in house mice. Evolution 63:20–28.
- 47. Immler S, Pitnick S, Parker GA, Durrant KL, Lüpold S, et al. (2011) Resolving variation in the reproductive tradeoff between sperm size and number. PNAS 108:5325–5330.
- 48. Montoto LG, Magana C, Tourmente M, Martín-Coello J, Crespo C, et al. (2011a) Sperm competition, sperm numbers and sperm quality in muroid rodents. PLoS One 6:e18173.
- 49. Napier RAN (1961) Fertility in the male rabbit. Journal of Reproduction and Fertility 2:273–289.
- 50. Beatty RA (1970) The genetics of the mammalian gamete. Biological Reviews 45:73–117.
- 51. Mossman J, Slate J, Humpries S, Birkhead T (2009) Sperm morphology and velocity are genetically codetermined in the zebra finch. Evolution 63:2730–2737.
- 52. Geraldes A, Basset P, Gibson B, Smith KL, Harr B, et al. (2008) Inferring the history of speciation in house mice from autosomal, X-linked, Y-linked and mitochondrial genes. Molecular Ecology 17:5349–5363.
- 53. White MA, Ane C, Dewey CN, Larget BR, Payseur BA (2009) Fine-scale phylogenetic discordance across the house mouse genome. PLOS Genetics 5:e1000729.
- 54. Keane TM, Goodstadt L, Danecek P, White MA, Wong K, et al. (2011) Mouse genomic variation and its effect on phenotypes and gene regulation. Nature 477:289–294.
- 55. Burgstaller JP, Johnston IG, Jones NS, Albrechtová J, Kolbe T, et al. (2014) mtDNA segregation in heteroplasmic tissues is common in vivo and modulated by haplotype differences and developmental stage. Cell Reports 7:2031–2041.