Spakovskiĭ G V, Lebedenko E N
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.
Bioorg Khim. 1998 Nov;24(11):877-80.
Full-length copies of cDNA of the hRPC11 gene encoding the smallest specific subunit of nuclear RNA polymerase III were identified among human transcripts with the use of the RT-PCR technique. The cloning of the first orthologue of the subunit RPC11 from a multicellular organism and the comparison of subunit hRPC11 of Homo sapiens (108 aa; M(r), 12.3 kDa; pI 8.05) deduced from the cDNA primary structure with the homologous components of RNA polymerase III from Saccharomyces cerevisiae and Schizosaccharomyces pombe revealed the most important functional domains: a Zn-binding motif of the classic type (CxxCx16-17CxxC) at the N-terminal region, and two extended regions of homology (KEVDDVLGG and RSADEPM) in the central and C-terminal parts of the molecule, respectively. The C-terminus of the RPC11 subunits is highly homologous to the unique zinc ribbon of the elongation factor TFIIS, which suggests a role for this subunit in the elongation or termination of RNA synthesis.
利用逆转录聚合酶链反应(RT-PCR)技术,在人类转录本中鉴定出了编码核RNA聚合酶III最小特异性亚基的hRPC11基因的全长cDNA拷贝。从多细胞生物中克隆出该亚基RPC11的首个直系同源物,并将从cDNA一级结构推导的智人亚基hRPC11(108个氨基酸;分子量12.3 kDa;等电点8.05)与酿酒酵母和粟酒裂殖酵母RNA聚合酶III的同源成分进行比较,揭示了最重要的功能域:N端区域的经典型锌结合基序(CxxCx16 - 17CxxC),以及分子中部和C端部分的两个延伸同源区域(KEVDDVLGG和RSADEPM)。RPC11亚基的C端与延伸因子TFIIS的独特锌带高度同源,这表明该亚基在RNA合成的延伸或终止中发挥作用。