Lawrie David S, Petrov Dmitri A
Department of Genetics, Stanford University, Stanford, CA, USA; Department of Biology, Stanford University, Stanford, CA, USA.
Department of Biology, Stanford University, Stanford, CA, USA.
Trends Genet. 2014 Apr;30(4):133-9. doi: 10.1016/j.tig.2014.02.002. Epub 2014 Mar 20.
The availability of sequenced genomes from multiple related organisms allows the detection and localization of functional genomic elements based on the idea that such elements evolve more slowly than neutral sequences. Although such comparative genomics methods have proven useful in discovering functional elements and ascertaining levels of functional constraint in the genome as a whole, here we outline limitations intrinsic to this approach that cannot be overcome by sequencing more species. We argue that it is essential to supplement comparative genomics with ultra-deep sampling of populations from closely related species to enable substantially more powerful genomic scans for functional elements. The convergence of sequencing technology and population genetics theory has made such projects feasible and has exciting implications for functional genomics.
多个相关生物体的测序基因组的可得性,使得基于功能基因组元件比中性序列进化更慢这一理念来检测和定位这些元件成为可能。尽管这种比较基因组学方法已被证明在发现功能元件以及确定整个基因组中的功能限制水平方面很有用,但在这里我们概述了这种方法固有的局限性,这些局限性无法通过对更多物种进行测序来克服。我们认为,用来自密切相关物种的群体的超深度抽样来补充比较基因组学至关重要,以便能够对功能元件进行实质上更强大的基因组扫描。测序技术与群体遗传学理论的融合使此类项目变得可行,并对功能基因组学具有令人兴奋的意义。