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噬菌体SP01末端重复序列中指定转录终止和暂停的区域。

Regions specifying transcriptional termination and pausing in the bacteriophage SP01 terminal repeat.

作者信息

Brennan S M, Geiduschek E P

出版信息

Nucleic Acids Res. 1983 Jun 25;11(12):4157-75. doi: 10.1093/nar/11.12.4157.

DOI:10.1093/nar/11.12.4157
PMID:6408611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC326031/
Abstract

We have determined the nucleotide sequences of four termination sites recognized by Bacillus subtilis RNA polymerase. These sites are located in the terminally repeated segment of the bacteriophage SP01 genome, where most early phage transcription occurs. The SP01 terminators have structures that are similar to those recognized by Escherichia coli RNA polymerase, containing a region of dyad symmetry followed by a stretch of HMU residues in the noncoding DNA strand (HMU is substituted for T in SP01 DNA). We note that in a terminator that is only 60% efficient in vitro, there is a greater distance between these two conserved elements that exists in more efficient terminators. We also find that RNA polymerase molecules which elongate a transcript through a partial terminator often pause at this site.

摘要

我们已经确定了枯草芽孢杆菌RNA聚合酶识别的四个终止位点的核苷酸序列。这些位点位于噬菌体SP01基因组的末端重复片段中,早期噬菌体转录大多在此处发生。SP01终止子具有与大肠杆菌RNA聚合酶识别的终止子相似的结构,包含一个二重对称区域,随后是非编码DNA链中的一段HMU残基(在SP01 DNA中,HMU替代了T)。我们注意到,在一个体外效率仅为60%的终止子中,这两个保守元件之间的距离比效率更高的终止子中的距离更大。我们还发现,通过部分终止子延伸转录本的RNA聚合酶分子经常在此位点暂停。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/8a5dfcb3547f/nar00357-0318-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/bbd700906b11/nar00357-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/164201bd0d92/nar00357-0313-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/5e9436d38d2d/nar00357-0316-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/8a5dfcb3547f/nar00357-0318-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/bbd700906b11/nar00357-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/164201bd0d92/nar00357-0313-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/5e9436d38d2d/nar00357-0316-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd06/326031/8a5dfcb3547f/nar00357-0318-a.jpg

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本文引用的文献

1
Pyrimidine-specific chemical reactions useful for DNA sequencing.用于DNA测序的嘧啶特异性化学反应。
Nucleic Acids Res. 1980 Oct 24;8(20):4613-9. doi: 10.1093/nar/8.20.4613.
2
Transcription of mouse rRNA genes by RNA polymerase I: in vitro and in vivo initiation and processing sites.RNA聚合酶I对小鼠rRNA基因的转录:体外和体内的起始及加工位点
Cell. 1981 Nov;27(1 Pt 2):165-74. doi: 10.1016/0092-8674(81)90370-6.
3
Termination of transcription and its regulation in the tryptophan operon of E. coli.大肠杆菌色氨酸操纵子中的转录终止及其调控。
Mol Gen Genet. 1989 Apr;216(2-3):364-71. doi: 10.1007/BF00334377.
Cell. 1981 Apr;24(1):10-23. doi: 10.1016/0092-8674(81)90496-7.
4
Spacer mutations in the lac ps promoter.乳糖操纵子启动子中的间隔突变
Proc Natl Acad Sci U S A. 1982 Feb;79(4):1069-72. doi: 10.1073/pnas.79.4.1069.
5
Changes in the association between Bacillus subtilis RNA polymerase core and two specificity-determining subunits during transcription.枯草芽孢杆菌RNA聚合酶核心与两个特异性决定亚基在转录过程中的关联变化。
Biochemistry. 1981 Nov 10;20(23):6564-9. doi: 10.1021/bi00526a007.
6
A lac promoter with a changed distance between -10 and -35 regions.一种在-10区和-35区之间距离发生改变的乳糖启动子。
Nucleic Acids Res. 1982 Feb 11;10(3):903-12. doi: 10.1093/nar/10.3.903.
7
Conserved nucleotide sequences in temporally controlled bacteriophage promoters.时间控制型噬菌体启动子中的保守核苷酸序列。
J Mol Biol. 1981 Oct 25;152(2):247-65. doi: 10.1016/0022-2836(81)90242-4.
8
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Virology. 1981 Jul 30;112(2):572-88. doi: 10.1016/0042-6822(81)90303-2.
9
A restriction map of the bacteriophage T4 genome.噬菌体T4基因组的限制酶切图谱。
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10
Sequencing end-labeled DNA with base-specific chemical cleavages.通过碱基特异性化学切割对末端标记的DNA进行测序。
Methods Enzymol. 1980;65(1):499-560. doi: 10.1016/s0076-6879(80)65059-9.