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影响大肠杆菌噬菌体λ的cII基因mRNA翻译效率的突变。

Mutations that affect the efficiency of translation of mRNA for the cII gene of coliphage lambda.

作者信息

Dul E, Mahoney M E, Wulff D L

出版信息

Genetics. 1987 Apr;115(4):585-90. doi: 10.1093/genetics/115.4.585.

DOI:10.1093/genetics/115.4.585
PMID:2953647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1203089/
Abstract

Starting with the lambda pRE-strain lambda ctr1 cy3008, which forms clear plaques, we have isolated two mutant strains, lambda dya2 ctr1 cy3008 and lambda dya3 ctr1 cy3008, that form plaques with very slightly turbid centers. The dya2 and dya3 mutations lie in the region of overlap between the PRE promoter and the ribosome recognition region of the cII gene, and have nucleotide alterations at positions -1 and +5 of pRE, and alterations in cII mRNA at -16 and -21 nucleotides before the initial AUG codon of the gene. Both mutations destabilize a stem structure that may be formed by cII mRNA, and dya2 also changes the sequence on cII mRNA that is complementary to the 3'-end of 16 S rRNA from 5'-UAAGGA-3' to 5'-UGAGGA-3'. --The dya2 and dya3 mutations, along with the ctr1 mutation, which destabilizes either of two alternate stem structures which may be formed by cII mRNA (these being more stable stem structures than the one affected by dya2 and dya3), were tested for their ability to reverse two cII-mutations that are characterized by inefficient translation of cII mRNA. These are cII3088, an A----G mutation four bases before the initial AUG codon, and cII3059, a GUU----GAU (Val2----Asp) second codon mutation. It was found that ctr1 completely reverses the translation defects of these two mutations, while dya2 partially reverses these translation defects. The dya3 mutation has no effect on translation efficiency under any condition tested.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

从形成清亮噬菌斑的λ pRE菌株λ ctr1 cy3008开始,我们分离出了两种突变菌株,λ dya2 ctr1 cy3008和λ dya3 ctr1 cy3008,它们形成的噬菌斑中心仅有轻微浑浊。dya2和dya3突变位于PRE启动子与cII基因核糖体识别区域的重叠区域,在pRE的 -1和 +5位置有核苷酸改变,在该基因起始AUG密码子之前的 -16和 -21核苷酸处cII mRNA有改变。这两种突变都使可能由cII mRNA形成的茎环结构不稳定,并且dya2还将cII mRNA上与16 S rRNA 3'端互补的序列从5'-UAAGGA-3'变为5'-UGAGGA-3'。——dya2和dya3突变,连同ctr1突变(其使可能由cII mRNA形成的两种交替茎环结构中的一种不稳定,这两种茎环结构比受dya2和dya3影响的更稳定),被测试了它们逆转两种以cII mRNA翻译效率低下为特征的cII突变的能力。这两种突变是cII3088,在起始AUG密码子前四个碱基处的A→G突变,以及cII3059,第二个密码子的GUU→GAU(Val2→Asp)突变。发现ctr1完全逆转了这两种突变的翻译缺陷,而dya2部分逆转了这些翻译缺陷。在任何测试条件下,dya3突变对翻译效率均无影响。(摘要截短至250字)

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3
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本文引用的文献

1
Characterization of translational initiation sites in E. coli.大肠杆菌中转录起始位点的表征
Nucleic Acids Res. 1982 May 11;10(9):2971-96. doi: 10.1093/nar/10.9.2971.
2
Promoter for the establishment of repressor synthesis in bacteriophage lambda.噬菌体λ中阻遏物合成建立的启动子。
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3191-5. doi: 10.1073/pnas.77.6.3191.
3
Control of transcription termination: a rho-dependent termination site in bacteriophage lambda.转录终止的调控:噬菌体λ中的一个ρ因子依赖性终止位点
J Mol Biol. 1980 Apr;138(2):231-54. doi: 10.1016/0022-2836(80)90285-5.
4
Structure and function of the cy control region of bacteriophage lambda.噬菌体λ的cy控制区的结构与功能
J Mol Biol. 1980 Apr;138(2):209-30. doi: 10.1016/0022-2836(80)90284-3.
5
lacZ translation initiation mutations.β-半乳糖苷酶翻译起始突变
J Mol Biol. 1984 Aug 25;177(4):663-83. doi: 10.1016/0022-2836(84)90043-3.
6
E. coli RNA polymerase interacts homologously with two different promoters.大肠杆菌RNA聚合酶与两种不同的启动子进行同源性相互作用。
Cell. 1980 Jun;20(2):269-81. doi: 10.1016/0092-8674(80)90613-3.
7
CII-dependent activation of the pRE promoter of coliphage lambda fused to the Escherichia coli galK gene.与大肠杆菌galK基因融合的λ噬菌体pRE启动子的CII依赖性激活。
Gene. 1984 Dec;32(1-2):141-50. doi: 10.1016/0378-1119(84)90042-8.
8
Mutations that alter the DNA binding site for the bacteriophage lambda cII protein and affect the translation efficiency of the cII gene.改变噬菌体λ cII蛋白DNA结合位点并影响cII基因翻译效率的突变。
J Mol Biol. 1984 Dec 25;180(4):865-80. doi: 10.1016/0022-2836(84)90261-4.
9
Mutational analysis of a regulatory region in bacteriophage lambda that has overlapping signals for the initiation of transcription and translation.对噬菌体λ中一个调控区域的突变分析,该区域具有转录和翻译起始的重叠信号。
Proc Natl Acad Sci U S A. 1984 Jan;81(2):555-9. doi: 10.1073/pnas.81.2.555.
10
The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites.大肠杆菌16S核糖体RNA的3'末端序列:与无义三联体及核糖体结合位点的互补性
Proc Natl Acad Sci U S A. 1974 Apr;71(4):1342-6. doi: 10.1073/pnas.71.4.1342.