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噬菌体Mu com基因似乎指定了mom基因表达所需的一种翻译因子。

The bacteriophage Mu com gene appears to specify a translation factor required for mom gene expression.

作者信息

Hattman S, Ives J, Wall L, Marić S

机构信息

Department of Biology, University of Rochester, NY 14627.

出版信息

Gene. 1987;55(2-3):345-51. doi: 10.1016/0378-1119(87)90295-2.

Abstract

Expression of the bacteriophage Mu mom gene is subject to a variety of regulatory controls. Both the host Dam DNA-adenine methylase and the phage Mu C protein are required for mom gene transcription. In addition, the Mu com gene product is required for production of the mom protein. Because the com and mom genes overlap on the same mRNA transcript (with com being located proximal to the 5' end), it is likely that Com function is exerted after transcription initiation. To study the role of Com, two segments of Mu were cloned in both orientations (+ and -) into the HindIII site of the galactokinase expression vector, pKG1800; the HindIII site is located between the galK structural gene and its promoter. In (+) plasmids, the Mu DNA inserts were transcribed from the gal promoter in the same orientation as in the phage genome; (-) plasmids had the Mu DNA inserted in the reverse orientation. Each Mu insert contained the same segment of the mom gene from the 3' terminus, but differed in the extent of com gene included at the 5' terminus; one contained a truncated com gene and the other a complete com gene, as well as upstream Mu regulatory sequences. The results are summarized as follows: (1) both (-) plasmids produced only about 10% as much galactokinase activity following fucose induction as the parental vector, pKG1800; (2) plasmid pGTVH(+), with an intact com gene produced about 30% as much galactokinase as pKG1800; (3) plasmid pMTVH(+), with a truncated com gene, produced only about 10% as much enzyme as pKG1800.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

噬菌体Mu的mom基因表达受到多种调控。mom基因转录需要宿主Dam DNA - 腺嘌呤甲基化酶和噬菌体Mu C蛋白。此外,Mu com基因产物是产生mom蛋白所必需的。由于com和mom基因在同一mRNA转录本上重叠(com位于5'端近端),Com功能可能在转录起始后发挥作用。为了研究Com的作用,将Mu的两个片段以两种方向(+和 - )克隆到半乳糖激酶表达载体pKG1800的HindIII位点;HindIII位点位于galK结构基因及其启动子之间。在(+)质粒中,Mu DNA插入片段从gal启动子以与噬菌体基因组相同的方向转录;( - )质粒中的Mu DNA以相反方向插入。每个Mu插入片段都包含来自3'末端的相同mom基因片段,但在5'末端包含的com基因范围不同;一个包含截短的com基因,另一个包含完整的com基因以及上游Mu调控序列。结果总结如下:(1)两种( - )质粒在岩藻糖诱导后产生的半乳糖激酶活性仅为亲本载体pKG1800的约10%;(2)具有完整com基因的质粒pGTVH(+)产生的半乳糖激酶约为pKG1800的30%;(3)具有截短com基因的质粒pMTVH(+)产生的酶仅为pKG1800的约10%。(摘要截断于250字)

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