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编码核糖体蛋白S1的大肠杆菌rpsA基因的DNA序列。

The DNA sequence of the gene rpsA of Escherichia coli coding for ribosomal protein S1.

作者信息

Schnier J, Isono K

出版信息

Nucleic Acids Res. 1982 Mar 25;10(6):1857-65. doi: 10.1093/nar/10.6.1857.

DOI:10.1093/nar/10.6.1857
PMID:6281725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC320576/
Abstract

The DNA sequence of the gene rpsA as well as of its neighboring regions has been determined using the dideoxyribonucleotide method. It was found that there is an "open-reading-frame" of 350 bp which precedes the gene rpsA. Furthermore, an extensive internal repeats of nucleotide sequence have been found in this gene.

摘要

已使用双脱氧核苷酸法测定了rpsA基因及其相邻区域的DNA序列。结果发现，在rpsA基因之前存在一个350bp的“开放阅读框”。此外，在该基因中还发现了广泛的核苷酸序列内部重复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce78/320576/5aa5a60c8d28/nar00375-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce78/320576/5aa5a60c8d28/nar00375-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce78/320576/5aa5a60c8d28/nar00375-0037-a.jpg

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本文引用的文献

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Nucleic Acids Res. 1980 Aug 25;8(16):3673-94. doi: 10.1093/nar/8.16.3673.
2
The major ribosome binding site of Escherichia coli ribosomal protein S1 is located in its N-terminal segment.大肠杆菌核糖体蛋白S1的主要核糖体结合位点位于其N端片段。
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Computer programs to analyze DNA and amino acid sequence data.用于分析DNA和氨基酸序列数据的计算机程序。
大肠杆菌smbA突变的多拷贝抑制基因mssA和mssB
Mol Gen Genet. 1994 Apr;243(1):9-16. doi: 10.1007/BF00283870.
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A subunit of an archaeal DNA-dependent RNA polymerase contains the S1 motif.古细菌依赖DNA的RNA聚合酶的一个亚基包含S1基序。
Nucleic Acids Res. 1994 Feb 25;22(4):694. doi: 10.1093/nar/22.4.694.
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Structure and expression of the gene encoding ribosomal protein S1 from the cyanobacterium Synechococcus sp. strain PCC 6301: striking sequence similarity to the chloroplast ribosomal protein CS1.
Mol Gen Genet. 1995 Jan 20;246(2):142-7. doi: 10.1007/BF00294676.
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Transcriptional organization of the rpsA operon of Escherichia coli.大肠杆菌rpsA操纵子的转录组织
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Appl Environ Microbiol. 1983 Jul;46(1):37-43. doi: 10.1128/aem.46.1.37-43.1983.
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Linkage map of Escherichia coli K-12, edition 7.大肠杆菌K-12连锁图谱，第7版。
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Determination of the promoter strength in the mixed transcription system. II. Promoters of ribosomal RNA, ribosomal protein S1 and recA protein operons from Escherichia coli.混合转录系统中启动子强度的测定。II. 大肠杆菌核糖体RNA、核糖体蛋白S1和recA蛋白操纵子的启动子
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Nucleic Acids Res. 1983 Apr 25;11(8):2237-55. doi: 10.1093/nar/11.8.2237.
Nucleic Acids Res. 1982 Jan 11;10(1):85-9. doi: 10.1093/nar/10.1.85.
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Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing.利用单链噬菌体克隆辅助快速DNA测序。
J Mol Biol. 1980 Oct 25;143(2):161-78. doi: 10.1016/0022-2836(80)90196-5.
5
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A rapid enzymatic DNA sequencing technique: determination of sequence alterations in early simian virus 40 temperature sensitive and deletion mutants.一种快速酶促DNA测序技术：猿猴病毒40早期温度敏感型和缺失突变体序列改变的测定
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