Cameron R Andrew, Chow Suk Hen, Berney Kevin, Chiu Tsz-Yeung, Yuan Qiu-Autumn, Krämer Alexander, Helguero Argelia, Ransick Andrew, Yun Mirong, Davidson Eric H
Division of Biology and Center for Computational Regulatory Genomics of the Beckman Institute, California Institute of Technology, Pasadena, CA 91125, USA.
Proc Natl Acad Sci U S A. 2005 Aug 16;102(33):11769-74. doi: 10.1073/pnas.0505291102. Epub 2005 Aug 8.
The DNA of functional cis-regulatory modules displays extensive sequence conservation in comparisons of genomes from modestly distant species. Patches of sequence that are several hundred base pairs in length within these modules are often seen to be 80-95% identical, although the flanking sequence cannot even be aligned. However, it is unlikely that base pairs located between the transcription factor target sites of cis-regulatory modules have sequence-dependent function, and the mechanism that constrains evolutionary change within cis-regulatory modules is incompletely understood. We chose five functionally characterized cis-regulatory modules from the Strongylocentrotus purpuratus (sea urchin) genome and obtained orthologous regulatory and flanking sequences from a bacterial artificial chromosome genome library of a congener, Strongylocentrotus franciscanus. As expected, single-nucleotide substitutions and small indels occur freely at many positions within the regulatory modules of these two species, as they do outside the regulatory modules. However, large indels (>20 bp) are statistically almost absent within the regulatory modules, although they are common in flanking intergenic or intronic sequence. The result helps to explain the patterns of evolutionary sequence divergence characteristic of cis-regulatory DNA.
在对亲缘关系稍远的物种的基因组进行比较时,功能性顺式调控模块的DNA表现出广泛的序列保守性。在这些模块中,长度为几百个碱基对的序列片段常常显示出80%至95%的同一性,尽管其侧翼序列甚至无法比对。然而,位于顺式调控模块的转录因子靶位点之间的碱基对不太可能具有序列依赖性功能,并且限制顺式调控模块内进化变化的机制尚未完全明了。我们从紫球海胆基因组中选择了五个功能已明确的顺式调控模块,并从同属的加州海胆的细菌人工染色体基因组文库中获得了直系同源的调控序列和侧翼序列。不出所料,这两个物种的调控模块内的许多位置自由地发生单核苷酸替换和小的插入缺失,就像在调控模块之外一样。然而,调控模块内统计上几乎不存在大的插入缺失(>20 bp),尽管它们在侧翼基因间序列或内含子序列中很常见。这一结果有助于解释顺式调控DNA的进化序列分歧特征模式。