Center for Ecology and Evolutionary Biology, University of Oregon, Eugene, OR 97403, USA.
J Hered. 2010 Mar-Apr;101 Suppl 1(Suppl 1):S62-74. doi: 10.1093/jhered/esq003. Epub 2010 Mar 8.
Caenorhabditis elegans is an androdioecious nematode with both hermaphrodites and males. Although males can potentially play an important role in avoiding inbreeding and facilitating adaptation, their existence is evolutionarily problematic because they do not directly generate offspring in the way that hermaphrodites do. This review explores how genetic, population genomic, and experimental evolution approaches are being used to address the role of males and outcrossing within C. elegans. Although theory suggests that inbreeding depression and male mating ability should be the primary determinants of male frequency, this has yet to be convincingly confirmed experimentally. Genomic analysis of natural populations finds that outcrossing occurs at low, but not negligible levels, and that observed patterns of linkage disequilibrium consistent with strong selfing may instead be generated by natural selection against outcrossed progeny. Recent experimental evolution studies suggest that males can be maintained at fairly high levels if populations are initiated with sufficient genetic variation and/or subjected to strong natural selection via a change in the environment. For example, as reported here, populations adapting to novel laboratory rearing and temperature regimes maintain males at frequencies from 5% to 40%. Laboratory and field results still await full reconciliation, which may be facilitated by identifying the loci underlying among-strain differences in mating system dynamics.
秀丽隐杆线虫是一种雌雄同体的雌雄同体线虫,既有雌雄同体,也有雄性。尽管雄性可能在避免近亲繁殖和促进适应方面发挥重要作用,但它们的存在在进化上存在问题,因为它们不像雌雄同体那样直接产生后代。本综述探讨了遗传、群体基因组和实验进化方法如何用于解决雄性和雌雄同体在秀丽隐杆线虫中的作用。尽管理论表明,近亲繁殖衰退和雄性交配能力应该是雄性频率的主要决定因素,但这尚未得到令人信服的实验证实。对自然种群的基因组分析发现,异交发生在低水平,但并非可以忽略不计的水平,并且观察到的与强烈自交一致的连锁不平衡模式可能是由自然选择对异交后代的排斥产生的。最近的实验进化研究表明,如果种群具有足够的遗传变异和/或通过环境变化受到强烈的自然选择,则可以维持相当高的雄性水平。例如,正如这里所报道的,适应新的实验室饲养和温度条件的种群将雄性维持在 5%到 40%的频率。实验室和现场的结果仍有待完全协调,这可以通过确定交配系统动态中菌株间差异的基因座来实现。