School of Biological Sciences (A08), University of Sydney, Camperdown, NSW, 2006, Australia.
J Comp Physiol B. 2011 Jul;181(5):575-94. doi: 10.1007/s00360-011-0584-0. Epub 2011 May 15.
Squamate reptiles (lizards and snakes) offer a unique model system for testing hypotheses about the evolutionary transition from oviparity (egg-laying) to viviparity (live-bearing) in amniote vertebrates. The evolution of squamate viviparity has occurred remarkably frequently (>108 times) and has resulted in major changes in reproductive physiology. Such frequent changes in reproductive strategy pose two questions: (1) what are the molecular mechanisms responsible for the evolution of squamate viviparity? (2) Are these molecular mechanisms the same for separate origins of viviparity? Molecular approaches, such as RT-PCR, in situ hybridisation, Western blotting and immunofluorescence, have been invaluable for identifying genes and proteins that are involved in squamate placental development, materno-foetal immunotolerance, placental transport, placental angiogenesis, hormone synthesis and hormone receptor expression. However, the candidate-gene or -protein approach that has been used until now does not allow for de novo gene/protein discovery; results to date suggest that the reproductive physiologies of mammals and squamate reptiles are very similar, but this conclusion may simply be due to a limited capacity to study the subset of genes and proteins that are unique to reptiles. Progress has also been slowed by the lack of appropriate molecular and genomic resources for squamate reptiles. The advent of next-generation sequencing provides a relatively inexpensive way to conduct rapid high-throughput sequencing of genomes and transcriptomes. We discuss the potential use of next-generation sequencing technologies to analyse differences in gene expression between oviparous and viviparous squamates, provide important sequence information for reptiles, and generate testable hypotheses for the evolution of viviparity.
蜥蜴和蛇类等有鳞目爬行动物为测试羊膜脊椎动物从卵生(产卵)到胎生(活体生产)的进化转变假说提供了一个独特的模式系统。有鳞目动物胎生的进化发生得非常频繁(超过 108 次),并导致了生殖生理学的重大变化。生殖策略的这种频繁变化提出了两个问题:(1)是什么分子机制导致了有鳞目动物胎生的进化?(2)这些分子机制对于胎生的不同起源是否相同?RT-PCR、原位杂交、Western 印迹和免疫荧光等分子方法对于鉴定参与有鳞目胎盘发育、母胎免疫耐受、胎盘转运、胎盘血管生成、激素合成和激素受体表达的基因和蛋白质非常有价值。然而,到目前为止一直使用的候选基因或蛋白质方法不允许新基因/蛋白质的发现;迄今为止的结果表明,哺乳动物和有鳞目爬行动物的生殖生理学非常相似,但这一结论可能仅仅是由于研究爬行动物特有的基因和蛋白质子集的能力有限。由于缺乏有鳞目爬行动物的适当分子和基因组资源,进展也受到了阻碍。下一代测序技术的出现为快速高通量测序基因组和转录组提供了一种相对便宜的方法。我们讨论了下一代测序技术在分析卵生和胎生有鳞目动物之间基因表达差异、为爬行动物提供重要的序列信息以及为胎生的进化生成可测试假说方面的潜在用途。