Moriya H, Kasai H, Isono K
Department of Biology, Faculty of Science, Kobe University, Japan.
Nucleic Acids Res. 1995 Feb 25;23(4):595-8. doi: 10.1093/nar/23.4.595.
During the course of systematic nucleotide sequence analysis of the terC region of E.coli K-12 by using the ordered lambda phage clones, we found the presence of a gene, termed hrpA, that showed a high degree of sequence similarity to the PRP2, PRP16 and PRP22 genes of Saccharomyces cerevisiae. The products of these yeast genes are known to play their roles in mRNA splicing, and belong to a group of proteins collectively called the DEAH family. The hrpA gene is the first example of a DEAH family gene in prokaryotes. The N-terminal region of the protein it encodes contains conserved sequence stretches characteristic of an RNA helicase. Its molecular mass is calculated to be 146 kDa. Previously, a 135 kDa protein was identified by Moir et al. [J. Bacteriol. (1992) 174, 2102-2110] in this region which is most likely identical to that encoded by hrpA. The C-terminal region of the hrpA gene product seems to contain an RNA binding motif weakly resembling that of ribosomal protein S1 of E.coli. Disruption of the hrpA gene suggested that it is not essential for the growth of E.coli.
在使用有序λ噬菌体克隆对大肠杆菌K-12的terC区域进行系统核苷酸序列分析的过程中,我们发现了一个名为hrpA的基因,它与酿酒酵母的PRP2、PRP16和PRP22基因具有高度的序列相似性。已知这些酵母基因的产物在mRNA剪接中发挥作用,并且属于一组统称为DEAH家族的蛋白质。hrpA基因是原核生物中DEAH家族基因的首个实例。它所编码蛋白质的N端区域包含RNA解旋酶特有的保守序列片段。其分子量经计算为146 kDa。此前,Moir等人[《细菌学杂志》(1992年)174, 2102 - 2110]在该区域鉴定出一种135 kDa的蛋白质,它极有可能与hrpA所编码的蛋白质相同。hrpA基因产物的C端区域似乎包含一个与大肠杆菌核糖体蛋白S1的RNA结合基序微弱相似的基序。hrpA基因的破坏表明它对大肠杆菌的生长并非必需。