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突变改变的核糖体蛋白L7/L12的一级结构及其对细胞生长和翻译准确性的影响。

Primary structures of mutationally altered ribosomal protein L7/L12 and their effects on cellular growth and translational accuracy.

作者信息

Kirsebom L A, Amons R, Isaksson L A

出版信息

Eur J Biochem. 1986 May 2;156(3):669-75. doi: 10.1111/j.1432-1033.1986.tb09630.x.

DOI:10.1111/j.1432-1033.1986.tb09630.x
PMID:3516698
Abstract

The amino acid sequences of mutationally altered ribosomal protein L7/L12 from four different rplL mutants of Escherichia coli were determined and correlated with some features of the mutant ribosomes. Two of the rplL mutations are deletions around position 40, which give rise to a shortened hinge region between the two domains of L7/L12. The other two mutants harbor point mutations at position 74 (Gly----Asp) or at position 82 (Glu----Lys), which are in or close to an evolutionarily conserved sequence in the C-terminal domain. The two latter mutations are associated with decreased rates of growth and translational elongation. All four mutants show increased nonsense codon read-through in vivo. Ribosomes from one of the deletion mutants show clearly increased missense error rates in vitro.

摘要

测定了来自大肠杆菌四个不同rplL突变体的经突变改变的核糖体蛋白L7/L12的氨基酸序列,并将其与突变核糖体的一些特征相关联。其中两个rplL突变是40位左右的缺失,这导致L7/L12两个结构域之间的铰链区缩短。另外两个突变体在74位(甘氨酸→天冬氨酸)或82位(谷氨酸→赖氨酸)存在点突变,这些位置位于C端结构域中一个进化保守序列内或附近。后两个突变与生长速率和翻译延伸速率降低有关。所有四个突变体在体内均表现出无义密码子通读增加。其中一个缺失突变体的核糖体在体外显示出明显增加的错义错误率。

相似文献

1
Primary structures of mutationally altered ribosomal protein L7/L12 and their effects on cellular growth and translational accuracy.突变改变的核糖体蛋白L7/L12的一级结构及其对细胞生长和翻译准确性的影响。
Eur J Biochem. 1986 May 2;156(3):669-75. doi: 10.1111/j.1432-1033.1986.tb09630.x.
2
Involvement of ribosomal protein L7/L12 in control of translational accuracy.核糖体蛋白L7/L12参与翻译准确性的调控。
Proc Natl Acad Sci U S A. 1985 Feb;82(3):717-21. doi: 10.1073/pnas.82.3.717.
3
Mutations in ribosomal proteins L7/L12 perturb EF-G and EF-Tu functions.核糖体蛋白L7/L12中的突变会扰乱EF-G和EF-Tu的功能。
Biochimie. 1988 May;70(5):611-8. doi: 10.1016/0300-9084(88)90244-1.
4
Genetic implication for an interaction between release factor one and ribosomal protein L7/L12 in vivo.体内释放因子1与核糖体蛋白L7/L12之间相互作用的遗传学意义。
J Mol Biol. 1994 Oct 7;242(5):614-8. doi: 10.1006/jmbi.1994.1611.
5
Characterization of the region on protein L7/L12 involved in binding to ribosomal particles.对蛋白质L7/L12上与核糖体颗粒结合区域的特性描述。
Eur J Biochem. 1982 Nov 15;128(2-3):371-5. doi: 10.1111/j.1432-1033.1982.tb06974.x.
6
Deletion of C-terminal residues of Escherichia coli ribosomal protein L10 causes the loss of binding of one L7/L12 dimer: ribosomes with one L7/L12 dimer are active.删除大肠杆菌核糖体蛋白L10的C末端残基会导致一个L7/L12二聚体结合的丧失:含有一个L7/L12二聚体的核糖体具有活性。
Biochemistry. 2000 Apr 11;39(14):4075-81. doi: 10.1021/bi992621e.
7
A point mutation in ribosomal protein L7/L12 reduces its ability to form a compact dimer structure and to assemble into the GTPase center.核糖体蛋白L7/L12中的一个点突变降低了其形成紧密二聚体结构并组装到GTP酶中心的能力。
Biochemistry. 2003 Apr 29;42(16):4691-8. doi: 10.1021/bi027087g.
8
Escherichia coli ribosomal protein L10 is rapidly degraded when synthesized in excess of ribosomal protein L7/L12.当大肠杆菌核糖体蛋白L10的合成量超过核糖体蛋白L7/L12时,它会迅速降解。
J Bacteriol. 1990 Jan;172(1):431-6. doi: 10.1128/jb.172.1.431-436.1990.
9
Ribosomal protein L7/L12 is required for GTPase translation factors EF-G, RF3, and IF2 to bind in their GTP state to 70S ribosomes.核糖体蛋白L7/L12是GTP酶翻译因子EF-G、RF3和IF2以其GTP状态结合到70S核糖体所必需的。
FEBS J. 2017 Jun;284(11):1631-1643. doi: 10.1111/febs.14067. Epub 2017 Apr 10.
10
Mistranslation in twelve Escherichia coli ribosomal proteins. Cysteine misincorporation at neutral amino acid residues other than tryptophan.十二种大肠杆菌核糖体蛋白中的错误翻译。色氨酸以外的中性氨基酸残基处的半胱氨酸错误掺入。
Eur J Biochem. 1987 Nov 16;169(1):59-64. doi: 10.1111/j.1432-1033.1987.tb13580.x.

引用本文的文献

1
Alterations in the ribosomal protein bL12 of E. coli affecting the initiation, elongation and termination of protein synthesis.大肠杆菌核糖体蛋白 bL12 的改变影响蛋白质合成的起始、延伸和终止。
Biochimie. 2020 Aug;175:173-180. doi: 10.1016/j.biochi.2020.06.006. Epub 2020 Jun 20.
2
Alterations in ribosomal protein L19 that decrease the fidelity of translation.核糖体蛋白L19的改变会降低翻译的保真度。
Biochimie. 2016 Sep-Oct;128-129:122-6. doi: 10.1016/j.biochi.2016.07.015. Epub 2016 Jul 28.
3
Control of phosphate release from elongation factor G by ribosomal protein L7/12.
核糖体蛋白L7/12对延伸因子G释放磷酸盐的控制。
EMBO J. 2005 Dec 21;24(24):4316-23. doi: 10.1038/sj.emboj.7600884. Epub 2005 Nov 17.
4
Multiple defects in translation associated with altered ribosomal protein L4.与核糖体蛋白L4改变相关的翻译中的多种缺陷。
Nucleic Acids Res. 2004 Oct 27;32(19):5750-6. doi: 10.1093/nar/gkh913. Print 2004.
5
Functional interactions in vivo between suppressor tRNA and mutationally altered ribosomal protein S4.体内抑制性tRNA与突变型核糖体蛋白S4之间的功能相互作用。
Mol Gen Genet. 1986 Nov;205(2):240-7. doi: 10.1007/BF00430434.
6
Transfer ribonucleic acid-mediated suppression of termination codons in Escherichia coli.转移核糖核酸介导的大肠杆菌终止密码子抑制作用。
Microbiol Rev. 1988 Sep;52(3):354-74. doi: 10.1128/mr.52.3.354-374.1988.
7
Errors and alternatives in reading the universal genetic code.通用遗传密码解读中的错误与变体
Microbiol Rev. 1989 Sep;53(3):273-98. doi: 10.1128/mr.53.3.273-298.1989.
8
Ribosomal protein L7/L12 has a helix-turn-helix motif similar to that found in DNA-binding regulatory proteins.核糖体蛋白L7/L12具有一种螺旋-转角-螺旋基序,类似于在DNA结合调节蛋白中发现的基序。
Nucleic Acids Res. 1989 May 25;17(10):3757-62. doi: 10.1093/nar/17.10.3757.
9
Single-base mutations at position 2661 of Escherichia coli 23S rRNA increase efficiency of translational proofreading.大肠杆菌23S rRNA第2661位的单碱基突变提高了翻译校对效率。
J Bacteriol. 1992 Dec;174(24):7896-901. doi: 10.1128/jb.174.24.7896-7901.1992.