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首页> 外文期刊>Journal of bacteriology >The Lysis-Lysogeny Decision of Bacteriophage 933W: a 933W Repressor-Mediated Long-Distance Loop Has No Role in Regulating 933W PRM Activity
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The Lysis-Lysogeny Decision of Bacteriophage 933W: a 933W Repressor-Mediated Long-Distance Loop Has No Role in Regulating 933W PRM Activity

机译:噬菌体933W的裂解-溶原性决定:933W阻遏物介导的远距离回路没有调节933W PRM活动的作用。

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Our data show that unlike bacteriophage λ, repressor bound at OL of bacteriophage 933W has no role in regulation of 933W repressor occupancy of 933W OR3 or the transcriptional activity of 933W PRM. This finding suggests that a cooperative long-range loop between repressor tetramers bound at OR and OL does not form in bacteriophage 933W. Nonetheless, 933W forms lysogens, and 933W prophage display a threshold response to UV induction similar to related lambdoid phages. Hence, the long-range loop thought to be important for constructing a threshold response in lambdoid bacteriophages is dispensable. The lack of a loop requires bacteriophage 933W to use a novel strategy in regulating its lysis-lysogeny decisions. As part of this strategy, the difference between the repressor concentrations needed to bind OR2 and activate 933W PRM transcription or bind OR3 and repress transcription from PRM is <2-fold. Consequently, PRM is never fully activated, reaching only ~25% of the maximum possible level of repressor-dependent activation before repressor-mediated repression occurs. The 933W repressor also apparently does not bind cooperatively to the individual sites in OR and OL. This scenario explains how, in the absence of DNA looping, bacteriophage 933W displays a threshold effect in response to DNA damage and suggests how 933W lysogens behave as “hair triggers” with spontaneous induction occurring to a greater extent in this phage than in other lambdoid phages.
机译:我们的数据表明,与噬菌体λ不同,结合在噬菌体933W的O L 上的阻遏物对933W O R 3的933W阻遏物占有率或933W的转录活性没有调节作用P RM 。该发现表明在噬菌体933W中未结合在O R 和O L 处的阻遏物四聚体之间的协作性远程环。但是,933W会形成溶原原,而933W的噬菌体显示出对UV诱导的阈值响应,类似于相关的lambdoid噬菌体。因此,对于在lambdoid噬菌体中构建阈值响应至关重要的远程循环是可有可无的。缺少环需要噬菌体933W在调节其裂解-溶原性决定时使用新策略。作为此策略的一部分,结合O R 2和激活933W P RM 转录或结合O R 3所需的阻遏物浓度之间的差异并抑制P RM 的转录<2倍。因此,P RM 从未被完全激活,仅达到阻遏物介导的阻遏作用发生之前的最大可能水平(约25%)。 933W阻遏物显然也不能与O R 和O L 中的单个位点协同结合。这种情况说明了在没有DNA环的情况下,噬菌体933W如何显示对DNA损伤的阈值效应,并提出了933W溶原菌如何作为“发源”而在该噬菌体中比在其他lambdoid噬菌体中发生自发诱导的程度更高。 。

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