Acker J, Murroni O, Mattei M G, Kedinger C, Vigneron M
Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), Illkirch, Strasbourg, France.
Genomics. 1996 Feb 15;32(1):86-90. doi: 10.1006/geno.1996.0079.
The gene (POLR2L) encoding a 7.6-kDa subunit (hRPB7.6) of human RNA polymerase has been cloned. It compromises two exons, 116 and 227 bp, respectively, interspaced with an intron of about 2.1 kb. This gene, whose localization has been assigned to the short arm of chromosome 11 (position 11p15), is transcribed in HeLa cells as one major messenger RNA, which encodes a 67-residue polypeptide (7645 Da) that shares strong homologies with the corresponding subunits of other eukaryotic and archaeal RNA polymerase subunits. Like its yeast counterpart (ABC10 beta, encoded by the RPB10 gene), the hRPB7.6 subunit may be shared by all three classes of human nuclear RNA polymerase. Cysteine residues characteristic of an atypical zinc-binding domain are conserved in the homologous sequences of all six species analyzed. A small, related RNA polymerase subunit from vaccinia virus exhibits an identical set of cysteines, suggesting that these residues may be contribute to a crucial function in the multimeric RNA polymerases.
编码人RNA聚合酶7.6 kDa亚基(hRPB7.6)的基因(POLR2L)已被克隆。它由两个外显子组成,分别为116 bp和227 bp,中间间隔一个约2.1 kb的内含子。该基因的定位已确定在11号染色体短臂(位置11p15),在HeLa细胞中作为一种主要信使RNA进行转录,其编码一个67个残基的多肽(7645 Da),与其他真核生物和古细菌RNA聚合酶的相应亚基具有高度同源性。与酵母对应物(由RPB10基因编码的ABC10β)一样,hRPB7.6亚基可能为人类所有三类核RNA聚合酶所共有。在所有分析的六个物种的同源序列中,非典型锌结合结构域特有的半胱氨酸残基是保守的。来自痘苗病毒的一个小的相关RNA聚合酶亚基表现出相同的一组半胱氨酸,表明这些残基可能对多聚体RNA聚合酶的关键功能有贡献。