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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.

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/ff6bc47bceb8/jbacter00081-0020-a.jpg

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