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嗜热自养甲烷杆菌RNA聚合酶基因的克隆与物理图谱绘制,以及与其他产甲烷古细菌RNA聚合酶基因的同源性和基因顺序比较。

Cloning and physical mapping of RNA polymerase genes from Methanobacterium thermoautotrophicum and comparison of homologies and gene orders with those of RNA polymerase genes from other methanogenic archaebacteria.

作者信息

Schallenberg J, Moes M, Truss M, Reiser W, Thomm M, Stetter K O, Klein A

机构信息

Molekulargenetik, Fachbereich Biologie, Philipps-Universität, Marburg/Lahn, Federal Republic of Germany.

出版信息

J Bacteriol. 1988 May;170(5):2247-53. doi: 10.1128/jb.170.5.2247-2253.1988.

DOI:10.1128/jb.170.5.2247-2253.1988
PMID:2834336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC211114/
Abstract

The structural genes encoding the four largest subunits of RNA polymerase, A, B', B", and C, were physically mapped in Methanobacterium thermoautotrophicum Winter. The genes formed a cluster in the order B", B', A, C and had a common orientation. DNA hybridization experiments yielded different degrees of homology between RNA polymerase gene sequences of different species of Methanobacterium and Methanococcus voltae. No homology was detectable between Methanobacterium thermoautotrophicum and Methanosarcina barkeri. From Southern hybridization experiments in which probes of the four genes from Methanobacterium thermoautotrophicum Winter and restriction digests of the genomic DNAs of the different methanogens were used, a common gene order of the RNA polymerase genes could be deduced.

摘要

编码RNA聚合酶四个最大亚基A、B'、B''和C的结构基因在嗜热自养甲烷杆菌温特株中进行了物理定位。这些基因按B''、B'、A、C的顺序形成一个簇,且具有共同的方向。DNA杂交实验显示,不同种的甲烷杆菌和沃氏甲烷球菌的RNA聚合酶基因序列之间存在不同程度的同源性。嗜热自养甲烷杆菌和巴氏甲烷八叠球菌之间未检测到同源性。通过Southern杂交实验,使用嗜热自养甲烷杆菌温特株的四个基因探针和不同产甲烷菌基因组DNA的限制性酶切片段,可以推断出RNA聚合酶基因的共同基因顺序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b81/211114/04a376bd3cc4/jbacter00183-0257-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b81/211114/4f8255f66f5a/jbacter00183-0254-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b81/211114/2c1d5faf5ebc/jbacter00183-0256-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b81/211114/04a376bd3cc4/jbacter00183-0257-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b81/211114/4f8255f66f5a/jbacter00183-0254-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b81/211114/2c1d5faf5ebc/jbacter00183-0256-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b81/211114/04a376bd3cc4/jbacter00183-0257-a.jpg

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引用本文的文献

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2
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3
Cyanobacterial RNA polymerase genes rpoC1 and rpoC2 correspond to rpoC of Escherichia coli.蓝藻RNA聚合酶基因rpoC1和rpoC2与大肠杆菌的rpoC相对应。

本文引用的文献

1
Structural homology between different archaebacterial DNA-dependent RNA polymerases analyzed by immunological comparison of their components.通过对不同古细菌 DNA 依赖性 RNA 聚合酶成分的免疫比较分析其结构同源性。
EMBO J. 1983;2(5):751-5. doi: 10.1002/j.1460-2075.1983.tb01495.x.
2
Archaebacteria and eukaryotes possess DNA-dependent RNA polymerases of a common type.古细菌和真核生物拥有共同类型的依赖DNA的RNA聚合酶。
EMBO J. 1983;2(8):1291-4. doi: 10.1002/j.1460-2075.1983.tb01583.x.
3
Regulation of biosynthesis of the DNA-dependent RNA polymerase in Escherichia coli.
J Bacteriol. 1989 Apr;171(4):1967-73. doi: 10.1128/jb.171.4.1967-1973.1989.
4
Specific transcription of cloned Methanobacterium thermoautotrophicum transcription units by homologous RNA polymerase in vitro.克隆的嗜热自养甲烷杆菌转录单元在体外被同源RNA聚合酶特异性转录。
Nucleic Acids Res. 1990 Mar 25;18(6):1441-6. doi: 10.1093/nar/18.6.1441.
大肠杆菌中依赖DNA的RNA聚合酶生物合成的调控
Curr Top Cell Regul. 1980;17:89-136. doi: 10.1016/b978-0-12-152817-1.50008-0.
4
Genome complexity of methanogenic bacteria.产甲烷菌的基因组复杂性。
J Bacteriol. 1984 May;158(2):628-31. doi: 10.1128/jb.158.2.628-631.1984.
5
The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.pUC质粒,一种源自M13mp7的用于插入诱变和使用合成通用引物进行测序的系统。
Gene. 1982 Oct;19(3):259-68. doi: 10.1016/0378-1119(82)90015-4.
6
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.
7
Efficient isolation of genes by using antibody probes.使用抗体探针高效分离基因。
Proc Natl Acad Sci U S A. 1983 Mar;80(5):1194-8. doi: 10.1073/pnas.80.5.1194.
8
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
9
Characterization of foot-and-mouth disease virus gene products with antisera against bacterially synthesized fusion proteins.用针对细菌合成融合蛋白的抗血清对口蹄疫病毒基因产物进行特性鉴定。
J Virol. 1986 Mar;57(3):983-91. doi: 10.1128/JVI.57.3.983-991.1986.
10
Detection of specific sequences among DNA fragments separated by gel electrophoresis.在通过凝胶电泳分离的DNA片段中检测特定序列。
J Mol Biol. 1975 Nov 5;98(3):503-17. doi: 10.1016/s0022-2836(75)80083-0.