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枯草芽孢杆菌中DNA复制终止子的作用定义及极性

Definition and polarity of action of DNA replication terminators in Bacillus subtilis.

作者信息

Smith M T, Wake R G

机构信息

Department of Biochemistry, University of Sydney, N.S.W., Australia.

出版信息

J Mol Biol. 1992 Oct 5;227(3):648-57. doi: 10.1016/0022-2836(92)90214-5.

Abstract

The first stage in termination of chromosome replication in Bacillus subtilis involves arrest of the clockwise fork at the inverted repeat region (IRR), comprising the opposed IRI and IRII sequences, adjacent to the upstream region of the rtp gene, which encodes the replication terminator protein RTP. RTP binds to IRI and IRII. The ability of the IRR and its components to function as terminators, in conjunction with RTP, and their polarity of action have now been tested by the use of plasmids replicating in B. subtilis as unidirectional theta structures and into which potential terminator sequences were inserted in alternate orientations relative to fork movement. When the complete IRR was inserted into such plasmids and the new plasmids transferred into a B. subtilis strain overproducing RTP, it was able to block movement of a replication fork approaching from either direction. IRI and IRII were shown to function as polar terminators, each blocking movement of a fork when it approached from one particular direction but not the other. Furthermore, the polarity of action was in accordance with the IRR being able to operate as a replication fork trap. Thus, a fork approaching the IRR would pass through the first terminator encountered (IRI or IRII) and be halted by the second. The previously observed nonfunctioning of a particular orientation of chromosomal IRR as a fork arrest site probably reflects a limiting level of RTP in the cell. Interestingly, a 21 base-pair core sequence spanning a single RTP binding site within IRI (the 47 base-pair IRI contains 2 binding sites) was unable to arrest a fork approaching from either direction in the plasmid system. This suggests that both binding sites within an IR must be filled in order to function as an arrest site. It is possible that co-operative interaction between adjacent dimers within IRI or IRII provides the necessary conformation for causing fork arrest.

摘要

枯草芽孢杆菌染色体复制终止的第一阶段涉及顺时针方向的复制叉在反向重复区域(IRR)处停滞,该区域由相对的IRI和IRII序列组成,毗邻rtp基因的上游区域,rtp基因编码复制终止蛋白RTP。RTP与IRI和IRII结合。IRR及其组件作为终止子与RTP协同发挥作用的能力,以及它们的作用极性,现已通过使用在枯草芽孢杆菌中以单向θ结构复制的质粒进行了测试,并且相对于叉的移动以交替方向插入了潜在的终止子序列。当将完整的IRR插入此类质粒并将新质粒转移到过量产生RTP的枯草芽孢杆菌菌株中时,它能够阻止从任一方向接近的复制叉的移动。IRI和IRII被证明可作为极性终止子,当叉从一个特定方向接近时,它们各自阻止叉的移动,但从另一个方向接近时则不然。此外,作用极性与IRR能够作为复制叉陷阱发挥作用一致。因此,接近IRR的叉会穿过遇到的第一个终止子(IRI或IRII),并被第二个终止子阻止。先前观察到的染色体IRR的特定方向作为叉停滞位点不起作用,可能反映了细胞中RTP的有限水平。有趣的是,跨越IRI内单个RTP结合位点的21个碱基对的核心序列(47个碱基对的IRI包含2个结合位点)在质粒系统中无法阻止从任一方向接近的叉。这表明IR内的两个结合位点都必须被占据才能作为停滞位点发挥作用。IRI或IRII内相邻二聚体之间的协同相互作用可能为导致叉停滞提供必要的构象。

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