Laboratory of Bacterial Genetics, Centre for DNA Fingerprinting and Diagnostics, Hyderabad 500039, India.
Graduate Studies, Manipal Academy of Higher Education, Manipal 576104, India.
Nucleic Acids Res. 2020 Jan 24;48(2):847-861. doi: 10.1093/nar/gkz1152.
RNase E is a 472-kDa homo-tetrameric essential endoribonuclease involved in RNA processing and turnover in Escherichia coli. In its N-terminal half (NTH) is the catalytic active site, as also a substrate 5'-sensor pocket that renders enzyme activity maximal on 5'-monophosphorylated RNAs. The protein's non-catalytic C-terminal half (CTH) harbours RNA-binding motifs and serves as scaffold for a multiprotein degradosome complex, but is dispensable for viability. Here, we provide evidence that a full-length hetero-tetramer, composed of a mixture of wild-type and (recessive lethal) active-site mutant subunits, exhibits identical activity in vivo as the wild-type homo-tetramer itself ('recessive resurrection'). When all of the cognate polypeptides lacked the CTH, the active-site mutant subunits were dominant negative. A pair of C-terminally truncated polypeptides, which were individually inactive because of additional mutations in their active site and 5'-sensor pocket respectively, exhibited catalytic function in combination, both in vivo and in vitro (i.e. intragenic or allelic complementation). Our results indicate that adjacent subunits within an oligomer are separately responsible for 5'-sensing and cleavage, and that RNA binding facilitates oligomerization. We propose also that the CTH mediates a rate-determining initial step for enzyme function, which is likely the binding and channelling of substrate for NTH's endonucleolytic action.
RNase E 是一种 472 kDa 的同四聚体内切核糖核酸酶,参与大肠杆菌中 RNA 的加工和周转。其 N 端(NTH)包含催化活性位点,以及一个底物 5'传感器口袋,使酶在 5'单磷酸化 RNA 上具有最大活性。该蛋白的非催化 C 端(CTH)含有 RNA 结合基序,作为多蛋白降解体复合物的支架,但对生存能力是可有可无的。在这里,我们提供的证据表明,由野生型和(隐性致死)活性位点突变亚基混合组成的全长异四聚体,在体内表现出与野生型同四聚体本身相同的活性(“隐性复活”)。当所有同源多肽都缺乏 CTH 时,活性位点突变亚基表现出显性负效应。一对 C 端截断的多肽,由于其活性位点和 5'传感器口袋中的额外突变,分别丧失了活性,但在组合中表现出催化功能,无论是在体内还是体外(即基因内或等位基因互补)。我们的结果表明,寡聚体中的相邻亚基分别负责 5'感应和切割,并且 RNA 结合有助于寡聚体的形成。我们还提出,CTH 介导了酶功能的限速初始步骤,可能是 NTH 的内切核酸酶作用的底物结合和通道化。