Cao G J, Pogliano J, Sarkar N
Boston Biomedical Research Institute, MA 02114, USA.
Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11580-5. doi: 10.1073/pnas.93.21.11580.
We had earlier identified the pcnB locus as the gene for the major Escherichia coli poly(A) polymerase (PAP I). In this report, we describe the disruption and identification of a candidate gene for a second poly(A) polymerase (PAP II) by an experimental strategy which was based on the assumption that the viability of E. coli depends on the presence of either PAP I or PAP II. The coding region thus identified is the open reading frame f310, located at about 87 min on the E. coli chromosome. The following lines of evidence support f310 as the gene for PAP II: (i) the deduced peptide encoded by f310 has a molecular weight of 36,300, similar to the molecular weight of 35,000 estimated by gel filtration of PAP II; (ii) the deduced f310 product is a relatively hydrophobic polypeptide with a pI of 9.4, consistent with the properties of partially purified PAP II; (iii) overexpression of f310 leads to the formation of inclusion bodies whose solubilization and renaturation yields poly(A) polymerase activity that corresponds to a 35-kDa protein as shown by enzyme blotting; and (iv) expression of a f310 fusion construct with hexahistidine at the N-terminus of the coding region allowed purification of a poly(A) polymerase fraction whose major component is a 36-kDa protein. E. coli PAP II has no significant sequence homology either to PAP I or to the viral and eukaryotic poly(A) polymerases, suggesting that the bacterial poly(A) polymerases have evolved independently. An interesting feature of the PAP II sequence is the presence of sets of two paired cysteine and histidine residues that resemble the RNA binding motifs seen in some other proteins.
我们之前已确定pcnB基因座是大肠杆菌主要聚腺苷酸聚合酶(PAP I)的基因。在本报告中,我们描述了通过一种实验策略对第二种聚腺苷酸聚合酶(PAP II)的候选基因进行的破坏和鉴定,该策略基于大肠杆菌的生存能力取决于PAP I或PAP II的存在这一假设。由此确定的编码区是开放阅读框f310,位于大肠杆菌染色体上约87分钟处。以下几方面证据支持f310是PAP II的基因:(i)f310编码的推导肽分子量为36,300,与通过PAP II凝胶过滤估计的35,000分子量相似;(ii)推导的f310产物是一种相对疏水的多肽,pI为9.4,与部分纯化的PAP II的特性一致;(iii)f310的过表达导致包涵体形成,其溶解和复性产生聚腺苷酸聚合酶活性,如酶印迹所示,该活性对应于一种35 kDa的蛋白质;(iv)在编码区N端带有六组氨酸的f310融合构建体的表达使得能够纯化一种聚腺苷酸聚合酶组分,其主要成分是一种36 kDa的蛋白质。大肠杆菌PAP II与PAP I以及病毒和真核聚腺苷酸聚合酶均无明显的序列同源性,这表明细菌聚腺苷酸聚合酶是独立进化的。PAP II序列的一个有趣特征是存在两组成对的半胱氨酸和组氨酸残基,类似于在其他一些蛋白质中看到的RNA结合基序。