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High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells.

作者信息

Ching E, Attardi G

出版信息

Biochemistry. 1982 Jun 22;21(13):3188-95. doi: 10.1021/bi00256a024.

DOI:10.1021/bi00256a024
PMID:6285960
Abstract
摘要

相似文献

1
High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells.HeLa细胞线粒体翻译产物的高分辨率电泳分离及部分特性分析
Biochemistry. 1982 Jun 22;21(13):3188-95. doi: 10.1021/bi00256a024.
2
Identification of discrete electrophoretic components among the products of mitochondrial protein synthesis in HeLa cells.在HeLa细胞线粒体蛋白质合成产物中鉴定离散的电泳成分。
J Mol Biol. 1975 Aug 5;96(2):291-306. doi: 10.1016/0022-2836(75)90349-6.
3
Metabolic properties of the products of mitochondrial protein synthesis in HeLa cells.HeLa细胞中线粒体蛋白质合成产物的代谢特性
J Biol Chem. 1977 Mar 10;252(5):1702-11.
4
Antibodies against synthetic peptides reveal that the unidentified reading frame A6L, overlapping the ATPase 6 gene, is expressed in human mitochondria.针对合成肽的抗体表明，与ATPase 6基因重叠的未鉴定读码框A6L在人线粒体中表达。
Cell. 1983 Apr;32(4):1269-77. doi: 10.1016/0092-8674(83)90308-2.
5
Variant forms of mitochondrial translation products in yeast: evidence for location of determinants on mitochondrial DNA.酵母中线粒体翻译产物的变体形式：线粒体DNA上决定因素位置的证据。
Proc Natl Acad Sci U S A. 1976 Apr;73(4):1083-6. doi: 10.1073/pnas.73.4.1083.
6
In vivo labeling and analysis of human mitochondrial translation products.人线粒体翻译产物的体内标记与分析
Methods Enzymol. 1996;264:197-211. doi: 10.1016/s0076-6879(96)64020-8.
7
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.将与疾病相关的线粒体DNA缺失导入缺乏线粒体DNA的HeLa细胞会导致线粒体功能障碍。
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10614-8. doi: 10.1073/pnas.88.23.10614.
8
The biosynthesis of mitochondrial cytochromes.线粒体细胞色素的生物合成。
Subcell Biochem. 1974 Dec;3(4):275-309.
9
Biogenesis of mitochondrial proteins in HeLa cells.
Methods Enzymol. 1979;56:66-79. doi: 10.1016/0076-6879(79)56010-8.
10
Ribosome recycling defects modify the balance between the synthesis and assembly of specific subunits of the oxidative phosphorylation complexes in yeast mitochondria.核糖体循环缺陷改变了酵母线粒体中氧化磷酸化复合物特定亚基的合成与组装之间的平衡。
Nucleic Acids Res. 2016 Jul 8;44(12):5785-97. doi: 10.1093/nar/gkw490. Epub 2016 Jun 1.

引用本文的文献

1
Mitochondrial genetic control of assembly and function of complex I in mammalian cells.哺乳动物细胞中复合物I组装和功能的线粒体遗传控制
J Bioenerg Biomembr. 2001 Jun;33(3):251-7. doi: 10.1023/a:1010791204961.
2
Polymorphic sites and the mechanism of evolution in human mitochondrial DNA.人类线粒体DNA中的多态性位点与进化机制。
Genetics. 1984 Mar;106(3):479-99. doi: 10.1093/genetics/106.3.479.
3
Identification of the polypeptides encoded in the ATPase 6 gene and in the unassigned reading frames 1 and 3 of human mtDNA.鉴定人类线粒体DNA中ATPase 6基因以及未分配阅读框1和3所编码的多肽。
Proc Natl Acad Sci U S A. 1983 Sep;80(18):5535-9. doi: 10.1073/pnas.80.18.5535.
4
Polymorphisms of mitochondrially encoded proteins.
Am J Hum Genet. 1986 Feb;38(2):159-69.
5
Transcription and translation of mitochondrial DNA in interspecific somatic cell hybrids.
Mol Cell Biol. 1986 Jun;6(6):1951-7. doi: 10.1128/mcb.6.6.1951-1957.1986.
6
Computer prediction of peptide maps: assignment of polypeptides to human and mouse mitochondrial DNA genes by analysis of two-dimensional-proteolytic digest gels.
Am J Hum Genet. 1986 Apr;38(4):461-81.
7
Identification of the polypeptides encoded in the unassigned reading frames 2, 4, 4L, and 5 of human mitochondrial DNA.人类线粒体DNA未分配阅读框2、4、4L和5中编码的多肽的鉴定。
Proc Natl Acad Sci U S A. 1986 Mar;83(6):1563-7. doi: 10.1073/pnas.83.6.1563.
8
Internal frameshifts within the mitochondrial genes for cytochrome oxidase subunit II and maxicircle unidentified reading frame 3 of Leishmania tarentolae are corrected by RNA editing: evidence for translation of the edited cytochrome oxidase subunit II mRNA.利什曼原虫细胞色素氧化酶亚基II和大环未知阅读框3的线粒体基因内的内部移码通过RNA编辑得到校正：编辑后的细胞色素氧化酶亚基II mRNA可翻译的证据。
Proc Natl Acad Sci U S A. 1989 Aug;86(16):6220-4. doi: 10.1073/pnas.86.16.6220.
9
The role of mitochondrial DNA in Huntington's disease.线粒体DNA在亨廷顿舞蹈症中的作用。
J Mol Neurosci. 1989;1(2):129-36. doi: 10.1007/BF02896896.
10
Familial mitochondrial complex I deficiency with an abnormal mitochondrial encoded protein.伴有异常线粒体编码蛋白的家族性线粒体复合体I缺乏症。
J Inherit Metab Dis. 1989;12 Suppl 2:355-7. doi: 10.1007/BF03335421.