A meiotic driver alters sperm form and function in house mice: a possible example of spite

The ability to subvert independent assortment of chromosomes is found in many meiotic drivers, such as the t haplotype in house mice Mus musculus , in which the t -bearing chromosomal homolog is preferentially transmitted to offspring. This is explained by a poison-antidote system, in which developi...

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Veröffentlicht in:Chromosome research 2022-09, Vol.30 (2-3), p.151-164
Hauptverfasser: Winkler, Lennart, Lindholm, Anna K.
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Sprache:eng
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Zusammenfassung:The ability to subvert independent assortment of chromosomes is found in many meiotic drivers, such as the t haplotype in house mice Mus musculus , in which the t -bearing chromosomal homolog is preferentially transmitted to offspring. This is explained by a poison-antidote system, in which developing + and t sperm in testes of + / t males are exposed to ‘poison’ coded by t loci, from which t sperm are protected, allowing t sperm an overwhelming fertilisation advantage in monogamous matings. This system is thought to result in poorly and normally motile sperm subpopulations within + / t sperm, leaving t sperm unharmed. Conversely, we found that the fastest quartile of sperm from + / t males swam more slowly, both forwards and along their travel path, and had reduced straightness and linearity, compared to the fastest quartile of + / + sperm. Moreover, sperm from + / t males had shorter tails and narrower heads than + / + sperm, and these morphological differences covaried with motility differences. Finally, + / t traits did not show evidence of bimodal distributions. We conclude that the t haplotype drive results in lasting damage to the motility of both + and t developing sperm, although previous studies indicate that + must be more harmed than t sperm. This damage to all sperm may explain the low success of + / t males in sperm competition with + / + males, seen in earlier studies. We propose that the harm the t causes to itself could be termed ‘spiteful’, which may also be common to other gamete-harming meiotic drive systems.
ISSN:0967-3849
1573-6849
1573-6849
DOI:10.1007/s10577-022-09695-4