Chang Ssu-Jean, Hsieh Shih-Yang, Yuan Hanna S, Chak Kin-Fu
Institute of Biochemistry, National Yang Ming University, Shih-Pai, Taipei 11221, Taiwan, ROC.
Biochem Biophys Res Commun. 2002 Dec 13;299(4):613-20. doi: 10.1016/s0006-291x(02)02704-3.
Posttranscriptional control of the bactericidal ColE7 operon has been implicated by a feedback endonucleolytic cleavage of its own mRNA. The cleavage site has been located at the coding region of ceiE7, the second cistron of the ColE7 cea-cei-cel polycistronic transcript. Interestingly, Im7 protein, the translation product of ceiE7, is required for the specific cleavage. It was found that both sequence (GAUCUGAUU) flanking the cleavage site and the putative T1 stem-loop structure distal to the coding region of ceiE7 gene play a critical role for the specific cleavage of ceiE7-mRNA. Furthermore, we have verified that a di-nucleotide GG sequence located at the topmost position of the loop region of the putative stem-loop structure is essential for the specific cleavage of ceiE7-mRNA. Thus, our data reveal the existence of a novel mRNA degradative machinery for the regulation of the expression of ColE7 operon.
杀菌性ColE7操纵子的转录后调控与其自身mRNA的反馈性内切核酸酶切割有关。切割位点位于ColE7 cea-cei-cel多顺反子转录本第二个顺反子ceiE7的编码区。有趣的是,ceiE7的翻译产物Im7蛋白是特异性切割所必需的。研究发现,切割位点两侧的序列(GAUCUGAUU)以及ceiE7基因编码区远端的假定T1茎环结构对ceiE7-mRNA的特异性切割起着关键作用。此外,我们已经证实,位于假定茎环结构环区最顶端位置的二核苷酸GG序列对ceiE7-mRNA的特异性切割至关重要。因此,我们的数据揭示了一种用于调控ColE7操纵子表达的新型mRNA降解机制的存在。