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Cloning of the altered mRNA stability (ams) gene of Escherichia coli K-12.

作者信息

Claverie-Martin F, Diaz-Torres M R, Yancey S D, Kushner S R

机构信息

Department of Genetics, University of Georgia, Athens 30602.

出版信息

J Bacteriol. 1989 Oct;171(10):5479-86. doi: 10.1128/jb.171.10.5479-5486.1989.

DOI:10.1128/jb.171.10.5479-5486.1989
PMID:2477358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC210387/
Abstract

A temperature-sensitive mutation in the ams gene of Escherichia coli causes an increase in the chemical half-life of pulse-labeled RNA at the nonpermissive temperature. Using lambda clones containing DNA fragments from the 23- to 24-min region on the E. coli chromosome, we have isolated a 5.8-kilobase DNA fragment which, when present in a low-copy-number plasmid, complements the conditional lethality and increased mRNA stability associated with the ams-1 mutation. The approximate initiation site and the direction of transcription of the ams gene were determined from the size of truncated polypeptides produced by Tn1000 insertions and Bal 31 deletions. Overexpression of the ams locus by using a T7 RNA polymerase-promoter system permitted the identification of an ams-encoded polypeptide of 110 kilodaltons.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebca/210387/939416a20869/jbacter00176-0258-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebca/210387/d7d115f01b4a/jbacter00176-0257-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebca/210387/f83fd7b594e2/jbacter00176-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebca/210387/939416a20869/jbacter00176-0258-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebca/210387/d7d115f01b4a/jbacter00176-0257-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebca/210387/f83fd7b594e2/jbacter00176-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebca/210387/939416a20869/jbacter00176-0258-b.jpg

相似文献

1
Cloning of the altered mRNA stability (ams) gene of Escherichia coli K-12.
J Bacteriol. 1989 Oct;171(10):5479-86. doi: 10.1128/jb.171.10.5479-5486.1989.
2
The gene specifying RNase E (rne) and a gene affecting mRNA stability (ams) are the same gene.编码核糖核酸酶E的基因(rne)与一个影响信使核糖核酸稳定性的基因(ams)是同一个基因。
Mol Microbiol. 1991 Apr;5(4):851-5. doi: 10.1111/j.1365-2958.1991.tb00758.x.
3
RNase E, an endoribonuclease, has a general role in the chemical decay of Escherichia coli mRNA: evidence that rne and ams are the same genetic locus.核糖核酸酶E是一种内切核糖核酸酶,在大肠杆菌信使核糖核酸的化学降解中起普遍作用:rne和ams是同一基因座的证据。
Mol Microbiol. 1990 Dec;4(12):2127-35. doi: 10.1111/j.1365-2958.1990.tb00574.x.
4
Identification of polypeptides encoded by an Escherichia coli locus (hflA) that governs the lysis-lysogeny decision of bacteriophage lambda.鉴定由大肠杆菌基因座(hflA)编码的多肽,该基因座控制噬菌体λ的裂解-溶原决定。
J Bacteriol. 1987 Sep;169(9):4076-85. doi: 10.1128/jb.169.9.4076-4085.1987.
5
Genetic analysis of Escherichia coli urease genes: evidence for two distinct loci.
J Bacteriol. 1990 Dec;172(12):7138-44. doi: 10.1128/jb.172.12.7138-7144.1990.
6
The Ams (altered mRNA stability) protein and ribonuclease E are encoded by the same structural gene of Escherichia coli.Ams(mRNA稳定性改变)蛋白和核糖核酸酶E由大肠杆菌的同一个结构基因编码。
Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):1-5. doi: 10.1073/pnas.88.1.1.
7
Genetic studies of cleavage-initiated mRNA decay and processing of ribosomal 9S RNA show that the Escherichia coli ams and rne loci are the same.对切割起始的mRNA衰变和核糖体9S RNA加工的遗传学研究表明,大肠杆菌的ams和rne基因座是相同的。
Mol Microbiol. 1991 Apr;5(4):857-64. doi: 10.1111/j.1365-2958.1991.tb00759.x.
8
Cloning and expression in Escherichia coli of tryptophan genes from Streptomyces griseus IMRU 3570.
FEMS Microbiol Lett. 1990 Mar 1;56(1-2):201-5. doi: 10.1016/0378-1097(90)90151-f.
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Analysis of the altered mRNA stability (ams) gene from Escherichia coli. Nucleotide sequence, transcriptional analysis, and homology of its product to MRP3, a mitochondrial ribosomal protein from Neurospora crassa.大肠杆菌中改变的mRNA稳定性(ams)基因分析。核苷酸序列、转录分析及其产物与粗糙脉孢菌线粒体核糖体蛋白MRP3的同源性。
J Biol Chem. 1991 Feb 15;266(5):2843-51.
10
Cloning and characterization of the aerobic sn-glycerol-3-phosphate dehydrogenase structural gene glpD of Escherichia coli K-12.大肠杆菌K-12需氧型sn-甘油-3-磷酸脱氢酶结构基因glpD的克隆与特性分析
J Bacteriol. 1987 Feb;169(2):507-13. doi: 10.1128/jb.169.2.507-513.1987.

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Single amino acid changes in the predicted RNase H domain of Escherichia coli RNase G lead to complementation of RNase E deletion mutants.大肠杆菌 RNase G 的预测 RNase H 结构域中的单个氨基酸变化导致 RNase E 缺失突变体的互补。
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3

本文引用的文献

1
Cytoplasmic dot hybridization. Simple analysis of relative mRNA levels in multiple small cell or tissue samples.细胞质斑点杂交。对多个小细胞或组织样本中相对mRNA水平的简单分析。
J Biol Chem. 1982 Aug 10;257(15):8569-72.
2
Analysis of gene control signals by DNA fusion and cloning in Escherichia coli.通过在大肠杆菌中进行DNA融合和克隆分析基因控制信号。
J Mol Biol. 1980 Apr;138(2):179-207. doi: 10.1016/0022-2836(80)90283-1.
3
Replacement of the fip gene of Escherichia coli by an inactive gene cloned on a plasmid.用克隆在质粒上的无活性基因替换大肠杆菌的fip基因。
Intragenic suppressors of temperature-sensitive rne mutations lead to the dissociation of RNase E activity on mRNA and tRNA substrates in Escherichia coli.
温度敏感型rne突变的基因内抑制子导致大肠杆菌中核糖核酸酶E在信使核糖核酸和转运核糖核酸底物上的活性解离。
Nucleic Acids Res. 2008 Sep;36(16):5306-18. doi: 10.1093/nar/gkn476. Epub 2008 Aug 8.
4
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.
5
Escherichia coli mrsC is an allele of hflB, encoding a membrane-associated ATPase and protease that is required for mRNA decay.大肠杆菌mrsC是hflB的一个等位基因,编码一种与膜相关的ATP酶和蛋白酶,mRNA降解需要该酶。
J Bacteriol. 1998 Apr;180(7):1929-38. doi: 10.1128/JB.180.7.1929-1938.1998.
6
RNase E activity is conferred by a single polypeptide: overexpression, purification, and properties of the ams/rne/hmp1 gene product.核糖核酸酶E的活性由单一多肽赋予:ams/rne/hmp1基因产物的过表达、纯化及特性
Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):9006-10. doi: 10.1073/pnas.90.19.9006.
7
Functional interaction of heat shock protein GroEL with an RNase E-like activity in Escherichia coli.大肠杆菌中热休克蛋白GroEL与一种RNase E样活性的功能相互作用。
Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):277-81. doi: 10.1073/pnas.90.1.277.
8
ard-1: a human gene that reverses the effects of temperature-sensitive and deletion mutations in the Escherichia coli rne gene and encodes an activity producing RNase E-like cleavages.ard-1:一种人类基因,可逆转大肠杆菌rne基因中温度敏感型和缺失突变的影响,并编码产生类似核糖核酸酶E切割活性的物质。
Proc Natl Acad Sci U S A. 1994 Oct 25;91(22):10591-5. doi: 10.1073/pnas.91.22.10591.
9
Cleavages in the 5' region of the ompA and bla mRNA control stability: studies with an E. coli mutant altering mRNA stability and a novel endoribonuclease.ompA和bla mRNA 5'区域的切割控制稳定性:对改变mRNA稳定性的大肠杆菌突变体和一种新型核糖核酸内切酶的研究。
EMBO J. 1990 Sep;9(9):2731-41. doi: 10.1002/j.1460-2075.1990.tb07460.x.
10
Specific endonucleolytic cleavage of the mRNA for ribosomal protein S20 of Escherichia coli requires the product of the ams gene in vivo and in vitro.大肠杆菌核糖体蛋白S20的信使核糖核酸(mRNA)的特异性核酸内切酶切割在体内和体外都需要ams基因的产物。
J Bacteriol. 1991 Apr;173(8):2488-97. doi: 10.1128/jb.173.8.2488-2497.1991.
J Bacteriol. 1984 Sep;159(3):1034-9. doi: 10.1128/jb.159.3.1034-1039.1984.
4
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.
5
Versatile low-copy-number plasmid vectors for cloning in Escherichia coli.用于在大肠杆菌中克隆的通用低拷贝数质粒载体。
Gene. 1982 Jun;18(3):335-41. doi: 10.1016/0378-1119(82)90172-x.
6
Novel bacteriophage lambda cloning vector.新型噬菌体λ克隆载体。
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5172-6. doi: 10.1073/pnas.77.9.5172.
7
Hybridization of denatured RNA transferred or dotted nitrocellulose paper.转移或点样在硝酸纤维素膜上的变性RNA的杂交。
Methods Enzymol. 1983;100:255-66. doi: 10.1016/0076-6879(83)00060-9.
8
Chromosomal location of a gene for chemical longevity of messenger ribonculeic acid in a temperature-sensitive mutant of Escherichia coli.大肠杆菌温度敏感突变体中信使核糖核酸化学寿命相关基因的染色体定位。
J Bacteriol. 1980 Apr;142(1):325-6. doi: 10.1128/jb.142.1.325-326.1980.
9
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.
10
Bacterial mutants which block phage assembly.阻断噬菌体组装的细菌突变体。
J Supramol Struct. 1974;2(2-4):349-59. doi: 10.1002/jss.400020224.