Vinogradov Alexander E, Anatskaya Olga V
Institute of Cytology, Russian Academy of Sciences, Tikhoretsky Avenue 4, St. Petersburg 194064, Russia.
Nucleic Acids Res. 2007;35(19):6350-6. doi: 10.1093/nar/gkm723. Epub 2007 Sep 18.
We present a molecular and cellular phenomenon underlying the intriguing increase in phenotypic organizational complexity. For the same set of human-mouse orthologous genes (11 534 gene pairs) and homologous tissues (32 tissue pairs), human shows a greater fraction of tissue-specific genes and a greater ratio of the total expression of tissue-specific genes to housekeeping genes in each studied tissue, which suggests a generally higher level of evolutionary cell differentiation (specialization). This phenomenon is spectacularly more pronounced in those human tissues that are more directly involved in the increase of complexity, longevity and body size (i.e. it is reflected on the organismal level as well). Genes with a change in expression breadth show a greater human-mouse divergence of promoter regions and encoded proteins (i.e. the functional genomics data are supported by the structural analysis). Human also shows the higher expression of translation machinery. The upstream untranslated regions (5'UTRs) of human mRNAs are longer than mouse 5'UTRs (even after correction for the difference in genome sizes) and contain more uAUG codons, which suggest a more complex regulation at the translational level in human cells (and agrees well with the augmented cell specialization).
我们展示了一种分子和细胞现象,它是表型组织复杂性有趣增加的基础。对于同一组人鼠直系同源基因(11534 个基因对)和同源组织(32 个组织对),在每个研究的组织中,人类显示出更高比例的组织特异性基因,以及组织特异性基因总表达量与管家基因总表达量的更高比例,这表明进化细胞分化(特化)的总体水平更高。这种现象在那些更直接参与复杂性、寿命和体型增加的人类组织中更为显著(即在生物体水平上也有所体现)。表达广度发生变化的基因在启动子区域和编码蛋白方面显示出更大的人鼠差异(即功能基因组学数据得到结构分析的支持)。人类还显示出翻译机制的更高表达。人类 mRNA 的上游非翻译区(5'UTRs)比小鼠的 5'UTRs 更长(即使在校正基因组大小差异之后),并且包含更多的 uAUG 密码子,这表明人类细胞在翻译水平上存在更复杂的调控(并且与增强的细胞特化非常吻合)。