Evans Patrick D, Vallender Eric J, Lahn Bruce T
Howard Hughes Medical Institute, Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
Gene. 2006 Jun 21;375:75-9. doi: 10.1016/j.gene.2006.02.019. Epub 2006 Mar 14.
Primary microcephaly is a developmental defect of the brain characterized by severely reduced brain size but an absence of other overt abnormalities. Mutations in several loci have been linked to primary microcephaly. The underlying genes for two of these were recently identified as CDK5RAP2 and CENPJ. Here, we focus on CDK5RAP2 and show that the protein evolutionary rate of this gene is significantly higher in primates than rodents or carnivores. We further show that the evolutionary rate within primates is particularly high in the human and chimpanzee terminal branches. Thus, the pattern of molecular evolution seen in CDK5RAP2 appears to parallel, at least approximately, that seen in two other previously identified primary microcephaly genes, microcephalin and ASPM. We also briefly discuss CENPJ, which similarly exhibits higher rate of protein evolution in primates as compared to rodents and carnivores. Together, the evolutionary patterns of all four presently known primary microcephaly genes are consistent with the hypothesis that genes regulating brain size during development might also play a role in brain evolution in primates and especially humans.
原发性小头畸形是一种大脑发育缺陷,其特征是脑容量严重减小,但无其他明显异常。多个基因座的突变与原发性小头畸形有关。其中两个基因座的相关基因最近被鉴定为CDK5RAP2和CENPJ。在此,我们聚焦于CDK5RAP2,并表明该基因在灵长类动物中的蛋白质进化速率显著高于啮齿动物或食肉动物。我们进一步表明,在灵长类动物中,人类和黑猩猩分支末端的进化速率尤其高。因此,CDK5RAP2中观察到的分子进化模式似乎至少大致与另外两个先前鉴定的原发性小头畸形基因——小头畸形基因(MCPH1)和异常纺锤体样微管相关蛋白(ASPM)中观察到的模式相似。我们还简要讨论了CENPJ,与啮齿动物和食肉动物相比,它在灵长类动物中同样表现出较高的蛋白质进化速率。总之,所有四个目前已知的原发性小头畸形基因的进化模式都与以下假设一致:在发育过程中调节脑容量的基因可能在灵长类动物尤其是人类的大脑进化中也发挥作用。