Zhang Jianzhi, Dyer Kimberly D, Rosenberg Helene F
Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Nucleic Acids Res. 2002 Mar 1;30(5):1169-75. doi: 10.1093/nar/30.5.1169.
We report the identification and characterization of the gene encoding the eighth and final human ribonuclease (RNase) of the highly diversified RNase A superfamily. The RNase 8 gene is linked to seven other RNase A superfamily genes on chromosome 14. It is expressed prominently in the placenta, but is not detected in any other tissues examined. Phylogenetic analysis suggests that RNase 7 is the closest relative of RNase 8 and that the pair likely resulted from a recent gene duplication event in primates. Further analysis reveals that the RNase 8 gene has incorporated non-silent mutations at an elevated rate (1.3 x 10(-9) substitutions/site/year) and that orthologous RNase 8 genes from 6 of 10 primate species examined have been deactivated by frameshifting deletions or point mutations at crucial structural or catalytic residues. The ribonucleolytic activity of recombinant human RNase 8 is among the lowest of members of this superfamily and it exhibits neither antiviral nor antibacterial activities characteristic of some other RNase A ribonucleases. The rapid evolution, species-limited deactivation and tissue-specific expression of RNase 8 suggest a unique physiological function and reiterates the evolutionary plasticity of the RNase A superfamily.
我们报告了高度多样化的核糖核酸酶A超家族中第八种也是最后一种人类核糖核酸酶(RNase)编码基因的鉴定与特性分析。核糖核酸酶8基因与14号染色体上的其他七个核糖核酸酶A超家族基因相连。它在胎盘中显著表达,但在检测的任何其他组织中均未检测到。系统发育分析表明,核糖核酸酶7是核糖核酸酶8的最亲近亲属,这一对基因可能源于灵长类动物近期的基因复制事件。进一步分析显示,核糖核酸酶8基因以较高的速率(1.3×10⁻⁹替换/位点/年)纳入了非同义突变,并且在所检测的10种灵长类动物中的6种的直系同源核糖核酸酶8基因已因关键结构或催化残基处的移码缺失或点突变而失活。重组人核糖核酸酶8的核糖核酸水解活性在该超家族成员中是最低的,并且它既不表现出其他一些核糖核酸酶A核糖核酸酶所具有的抗病毒活性,也不表现出抗菌活性。核糖核酸酶8的快速进化、物种限制失活和组织特异性表达表明其具有独特的生理功能,并再次强调了核糖核酸酶A超家族的进化可塑性。