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大肠杆菌K-12的ilvGMEDA基因簇编码的多个转录本。

Multiple transcripts encoded by the ilvGMEDA gene cluster of Escherichia coli K-12.

作者信息

Huang F, Coppola G, Calhoun D H

机构信息

Department of Chemistry, City College of New York, New York 10031.

出版信息

J Bacteriol. 1992 Aug;174(15):4871-7. doi: 10.1128/jb.174.15.4871-4877.1992.

DOI:10.1128/jb.174.15.4871-4877.1992
PMID:1629149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC206297/
Abstract

We report here that, using Northern (RNA) blots, we identified two relatively stable transcripts of 4.6 and 1.1 kb that correspond to the products of the ilvEDA and ilvE genes and two relatively unstable transcripts of 6.7 and 3.6 kb that correspond to the products of the ilvGMEDA and ilvDA genes. The transcripts were identified by the use of eight probes derived from segments of the ilvGMEDA cluster. In addition, we used two strains with deletions of ilvG or ilvDA and observed the expected decrease in transcript size in Northern blots. Primer extension with reverse transcriptase generated a 169-nucleotide product corresponding to a 5' end within the ilvED intercistronic region, 37 nucleotides from the AUG codon of the ilvD gene. This primer extension product presumably indicates the 5' end of the ilvDA transcript that we detected in Northern blots. The stability of the transcripts was monitored, and RNase E was found to play a major role in ilv transcript degradation. Transcript levels varied in response to growth in the presence of the end product amino acids and in response to the presence of the polar frameshift site in ilvG. Although there have been speculations about the identities and numbers of transcripts derived from the ilvGMEDA cluster on the basis of the identification of some of the sites of transcription initiation and termination, this is the first report of the use of Northern blots to determine the actual sizes and distribution of mRNAs present in vivo.

摘要

我们在此报告,通过Northern(RNA)印迹法,我们鉴定出了两种相对稳定的转录本,分别为4.6 kb和1.1 kb,它们对应于ilvEDA和ilvE基因的产物,以及两种相对不稳定的转录本,分别为6.7 kb和3.6 kb,它们对应于ilvGMEDA和ilvDA基因的产物。这些转录本是通过使用源自ilvGMEDA簇片段的8种探针鉴定出来的。此外,我们使用了ilvG或ilvDA缺失的两种菌株,并在Northern印迹中观察到转录本大小出现了预期的减小。用逆转录酶进行引物延伸产生了一个169个核苷酸的产物,其对应于ilvED基因间区域内的一个5'端,距离ilvD基因的AUG密码子37个核苷酸。这个引物延伸产物大概表明了我们在Northern印迹中检测到的ilvDA转录本的5'端。我们监测了转录本的稳定性,发现RNase E在ilv转录本降解中起主要作用。转录本水平会因终产物氨基酸存在时的生长情况以及ilvG中极性移码位点的存在而发生变化。尽管基于转录起始和终止位点的部分鉴定,人们对源自ilvGMEDA簇的转录本的身份和数量进行了推测,但这是首次使用Northern印迹法来确定体内存在的mRNA的实际大小和分布的报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/ac458a5afb1b/jbacter00081-0021-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/ff6bc47bceb8/jbacter00081-0020-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/8a63a95c8714/jbacter00081-0020-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/219d5ea589c8/jbacter00081-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/ac458a5afb1b/jbacter00081-0021-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/ff6bc47bceb8/jbacter00081-0020-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/8a63a95c8714/jbacter00081-0020-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/219d5ea589c8/jbacter00081-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adf/206297/ac458a5afb1b/jbacter00081-0021-b.jpg

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本文引用的文献

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Genetics. 1954 Jul;39(4):440-52. doi: 10.1093/genetics/39.4.440.
2
Organization and regulation of the ilvGEDA operon in Salmonella typhimurium LT2.鼠伤寒沙门氏菌LT2中ilvGEDA操纵子的组织与调控
J Bacteriol. 1981 Feb;145(2):984-9. doi: 10.1128/jb.145.2.984-989.1981.
3
Physical and genetic localization of ilv regulatory sites in lambda ilv bacteriophages.λilv噬菌体中ilv调控位点的物理定位和遗传定位
嗜柠檬酸明串珠菌citCDEF基因座的遗传组织以及mae和clyR基因的鉴定
J Bacteriol. 1999 Jul;181(14):4411-6. doi: 10.1128/JB.181.14.4411-4416.1999.
4
Elements involved in catabolite repression and substrate induction of the lactose operon in Lactobacillus casei.干酪乳杆菌中乳糖操纵子的分解代谢物阻遏和底物诱导所涉及的元件。
J Bacteriol. 1999 Jul;181(13):3928-34. doi: 10.1128/JB.181.13.3928-3934.1999.
5
Linkage map of Escherichia coli K-12, edition 10: the traditional map.大肠杆菌K-12连锁图谱,第10版:传统图谱。
Microbiol Mol Biol Rev. 1998 Sep;62(3):814-984. doi: 10.1128/MMBR.62.3.814-984.1998.
6
Multiple transcriptional control of the Lactococcus lactis trp operon.乳酸乳球菌色氨酸操纵子的多重转录调控
J Bacteriol. 1998 Jun;180(12):3174-80. doi: 10.1128/JB.180.12.3174-3180.1998.
7
Rgg is a positive transcriptional regulator of the Streptococcus gordonii gtfG gene.Rgg是戈登链球菌gtfG基因的一种正向转录调节因子。
J Bacteriol. 1996 Oct;178(19):5826-30. doi: 10.1128/jb.178.19.5826-5830.1996.
8
Isoleucine synthesis in Corynebacterium glutamicum: molecular analysis of the ilvB-ilvN-ilvC operon.谷氨酸棒杆菌中异亮氨酸的合成:ilvB-ilvN-ilvC操纵子的分子分析
J Bacteriol. 1993 Sep;175(17):5595-603. doi: 10.1128/jb.175.17.5595-5603.1993.
9
Functions of the gene products of Escherichia coli.大肠杆菌基因产物的功能。
Microbiol Rev. 1993 Dec;57(4):862-952. doi: 10.1128/mr.57.4.862-952.1993.
J Bacteriol. 1982 Mar;149(3):1071-81. doi: 10.1128/jb.149.3.1071-1081.1982.
4
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5
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6
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J Bacteriol. 1973 Apr;114(1):195-207. doi: 10.1128/jb.114.1.195-207.1973.
7
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8
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9
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10
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J Bacteriol. 1985 May;162(2):598-606. doi: 10.1128/jb.162.2.598-606.1985.