Yue D, Maizels N, Weiner A M
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520-8114, USA.
RNA. 1996 Sep;2(9):895-908.
We describe the purification, cloning, and characterization of the CCA-adding enzyme [ATP(CTP):tRNA nucleotidyl transferase] from the thermophilic archaebacterium, Sulfolobus shibatae. Characterization of an archaeal CCA-adding enzyme provides formal proof that the CCA-adding activity is present in all three contemporary kingdoms. Antibodies raised against recombinant, expressed Sulfolobus CCA-adding enzyme reacted specifically with the 48-kDa protein and fully depleted all CCA-adding activity from S. shibatae crude extract. Thus, the cloned cca gene encodes the only CCA-adding activity in S. shibatae. Remarkably, the archaeal CCA-adding enzyme exhibits no strong homology to either the eubacterial or eukaryotic CCA-adding enzymes. Nonetheless, it does possess the active site signature G[SG][LIVMFY]xR[GQ]x5,6D[LIVM][CLIVMFY]3-5 of the nucleotidyltransferase superfamily identified by Holm and Sander (1995, Trends Biochem Sci 20:345-347) and sequence comparisons show that all known CCA-adding enzymes and poly(A) polymerases are contained within this superfamily. Moreover, we propose that the superfamily can now be divided into two (and possibly three) subfamilies: class I, which contains the archaeal CCA-adding enzyme, eukaryotic poly(A) polymerases, and DNA polymerase beta; class II, which contains eubacterial and eukaryotic CCA-adding enzymes, and eubacterial poly(A) polymerases; and possibly a third class containing eubacterial polynucleotide phosphorylases. One implication of these data is that there may have been intraconversion of CCA-adding and poly(A) polymerase activities early in evolution.
我们描述了从嗜热古细菌柴田硫化叶菌(Sulfolobus shibatae)中纯化、克隆并鉴定CCA添加酶[ATP(CTP):tRNA核苷酸转移酶]的过程。对古细菌CCA添加酶的鉴定提供了正式证据,证明CCA添加活性存在于所有三个现代生物界中。针对重组表达的硫化叶菌CCA添加酶产生的抗体与48 kDa的蛋白质发生特异性反应,并完全耗尽了柴田硫化叶菌粗提物中的所有CCA添加活性。因此,克隆的cca基因编码柴田硫化叶菌中唯一的CCA添加活性。值得注意的是,古细菌CCA添加酶与真细菌或真核生物的CCA添加酶均无强烈的同源性。尽管如此,它确实具有由霍尔姆和桑德(1995年,《生物化学趋势》20:345 - 347)鉴定的核苷酸转移酶超家族的活性位点特征G[SG][LIVMFY]xR[GQ]x5,6D[LIVM][CLIVMFY]3 - 5,序列比较表明所有已知的CCA添加酶和聚腺苷酸聚合酶都包含在这个超家族中。此外,我们提出这个超家族现在可以分为两个(可能是三个)亚家族:I类,包含古细菌CCA添加酶、真核生物聚腺苷酸聚合酶和DNA聚合酶β;II类,包含真细菌和真核生物的CCA添加酶以及真细菌聚腺苷酸聚合酶;可能还有第三类包含真细菌多核苷酸磷酸化酶。这些数据的一个含义是,在进化早期可能存在CCA添加和聚腺苷酸聚合酶活性的相互转化。