Skalka A M
Fox Chase Cancer Center, Institute for Cancer Research, Philadelphia, PA 19111.
Gene. 1993 Dec 15;135(1-2):175-82. doi: 10.1016/0378-1119(93)90063-9.
Phylogenetic comparisons of retroviral IN (integrase) protein sequences have revealed homologies that extend to the retrotransposon and bacterial transposase families and have provided evidence for at least two functional domains. The N-terminal region is characterized by a Zn-finger-like array which is conserved in retrotransposons. The central region is defined by a D,D(35)E amino acid constellation which is conserved through the retrotransposons and several bacterial IS element transposases. Mutagenesis studies and biochemical analysis of the isolated central D,D(35)E domain support our original suggestion that this region contains the catalytic center of these proteins which must all share a similar enzymatic mechanism. These, and other recent findings suggest unexpected relationships between diverse pathways of nucleic acid metabolism in eukaryotes and prokaryotes.
逆转录病毒整合酶(IN)蛋白序列的系统发育比较揭示了其与逆转座子和细菌转座酶家族的同源性,并为至少两个功能域提供了证据。N 端区域的特征是一个类似锌指的阵列,在逆转座子中保守。中央区域由 D,D(35)E 氨基酸序列组成,在逆转座子和几种细菌 IS 元件转座酶中保守。对分离出的中央 D,D(35)E 结构域的诱变研究和生化分析支持了我们最初的观点,即该区域包含这些蛋白质的催化中心,它们必定都共享相似的酶促机制。这些以及其他近期发现表明,真核生物和原核生物中核酸代谢的不同途径之间存在意想不到的关系。