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枯草芽孢杆菌中terC处复制叉停滞的DNA序列要求。

DNA sequence requirements for replication fork arrest at terC in Bacillus subtilis.

作者信息

Smith M T, Wake R G

机构信息

Department of Biochemistry, University of Sydney, New South Wales, Australia.

出版信息

J Bacteriol. 1988 Sep;170(9):4083-90. doi: 10.1128/jb.170.9.4083-4090.1988.

Abstract

The replication terminus, terC, of Bacillus subtilis is the chromosomal site at which movement of the clockwise replication fork is blocked. The effect of deletion or modification of DNA sequences on either side of terC (defined by the sequence location of the arrested clockwise fork junction) has been investigated. Deletion of sequences ahead of terC to within 250 base pairs (bp) had no effect on fork arrest, whereas removal of a further 130 bp abolished it. The 250-bp segment immediately ahead of terC encompassed the previously identified inverted repeat region as well as potential promoters for the transcription of an adjoining open reading frame (ORF). Deletion of DNA from the other side of terC up to 80 bp from it also abolished fork arrest. This deletion removed the bulk of the ORF. Disruption of this ORF by the insertion of 4 bp also abolished fork arrest. A model for clockwise fork arrest at terC, implicating both the inverted repeat region and the protein product of the ORF, is proposed.

摘要

枯草芽孢杆菌的复制终止位点terC是顺时针复制叉移动被阻断的染色体位点。已研究了terC两侧(由停滞的顺时针叉连接点的序列位置定义)DNA序列的缺失或修饰的影响。将terC之前的序列缺失至250个碱基对(bp)内对叉停滞没有影响,而进一步去除130 bp则消除了叉停滞。terC之前紧邻的250 bp片段包含先前鉴定的反向重复区域以及相邻开放阅读框(ORF)转录的潜在启动子。从terC另一侧删除直至距其80 bp的DNA也消除了叉停滞。该缺失去除了大部分ORF。通过插入4 bp破坏该ORF也消除了叉停滞。提出了一个terC处顺时针叉停滞的模型,涉及反向重复区域和ORF的蛋白质产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ef/211412/64a814860e46/jbacter00187-0306-a.jpg

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