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首页> 外文期刊>Journal of Molecular Biology >PROGRAMMED CELL DEATH BY HOK/SOK OF PLASMID R1 - PROCESSING AT THE HOK MRNA 3'-END TRIGGERS STRUCTURAL REARRANGEMENTS THAT ALLOW TRANSLATION AND ANTISENSE RNA BINDING
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PROGRAMMED CELL DEATH BY HOK/SOK OF PLASMID R1 - PROCESSING AT THE HOK MRNA 3'-END TRIGGERS STRUCTURAL REARRANGEMENTS THAT ALLOW TRANSLATION AND ANTISENSE RNA BINDING

机译:通过质粒/质粒的R / Hok编程的细胞死亡-在Hok的MRNA 3'-末端触发结构重组中进行处理,从而允许翻译和反义RNA结合

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The hok/sok locus of plasmid R1 mediates plasmid stabilization by killing of plasmid-free cells. The locus specifies two RNAs, hok mRNA and Sok antisense RNA. The post-segregational killing mediated by hok/sok is governed by a complicated control mechanism that involves both post-transcriptional inhibition of translation by Sok-RNA and activation of hok translation by mRNA 3' processing. Sok-RNA inhibits translation of a reading frame (mok) that overlaps with hok, and translation of hok is coupled to translation of mok. In the inactive full-length hok mRNA, the translational activator element at the mRNA 5'-end (tac) is sequestered by the fold-back-inhibitory element located at the mRNA 3'-end (fbi). The 5' to 3' pairing locks the RNA in an inert configuration in which the SDmok and Sok-RNA target regions are sequestered. Here we show that the 3' processing leads to major structural rearrangements in the mRNA 5'-end. The structure of the refolded RNA explains activation of translation and antisense RNA binding. The refolded RNA contains an antisense RNA target stem-loop that presents the target nucleotides in a single-stranded conformation. The stem of the target hairpin contains SDmok and AUG(mok) in a paired configuration. Using toeprinting analysis, we show that this pairing keeps SDmok in an accessible configuration. Furthermore, a mutational analysis shows that an internal loop in the target stem is prerequisite for efficient translation and antisense RNA binding. (C) 1997 Academic Press Limited. [References: 33]
机译:质粒R1的hok / sok基因座通过杀死无质粒的细胞来介导质粒稳定。该基因座指定了两个RNA,即hok mRNA和Sok反义RNA。由hok / sok介导的分离后杀伤由复杂的控制机制控制,该机制涉及转录后抑制Sok-RNA的翻译和激活mRNA的3'加工引起的hok翻译。 Sok-RNA抑制与hok重叠的阅读框(mok)的翻译,并且hok的翻译与mok的翻译偶联。在无活性的全长hok mRNA中,位于mRNA 5'末端(tac)的翻译激活因子被位于mRNA 3'末端(fbi)的折返抑制元件所隔离。 5'至3'配对将RNA锁定为惰性构型,其中SDmok和Sok-RNA靶区域被隔离。在这里,我们显示3'加工导致mRNA 5'端的主要结构重排。重新折叠的RNA的结构解释了翻译和反义RNA结合的激活。重新折叠的RNA包含反义RNA靶茎环,以单链构象呈递靶核苷酸。目标发夹的茎包含成对配置的SDmok和AUG(mok)。通过使用脚印分析,我们证明了该配对使SDmok保持在可访问的配置中。此外,突变分析表明目标茎中的内部环是有效翻译和反义RNA结合的前提。 (C)1997 Academic Press Limited。 [参考:33]

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