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酵母线粒体DNA中“断裂基因” cob 的表达。核突变特异性地阻断了其初级转录本中不同内含子的切除。

Expression of the "split gene" cob in yeast mtDNA. Nuclear mutations specifically block the excision of different introns from its primary transcript.

作者信息

Pillar T, Lang B F, Steinberger I, Vogt B, Kaudewitz F

出版信息

J Biol Chem. 1983 Jul 10;258(13):7954-9.

PMID:6345534
Abstract

Five nuclear mutants falling into five different complementation groups are shown to block the maturation of long form mitochondrial cob RNA at five different processing steps. At the same time they prevent complete processing of the oxi 3 RNA, thus exhibiting the same phenotype as mitochondrial box mutants (cyt b- and oxi 3-). The different nuclear factors in question have varying ranges of specificity for the removal of introns from cob RNA, from only one to at the most three introns. Two mutated nuclear elements are shown to be specific for the processing of introns present only in the long form cob gene. One such mutation shows, as expected, no deleterious effect on the processing of the short form cob RNA exchanged into the mutant via cytoduction. The role of nuclear coded factors in the possible translation or activity of introncoded products ("maturases") is discussed for two mutants. Striking parallels are found between diverse polypeptide products, presumably translated from accumulated cob RNA intermediates, in pet- and mit- mutants blocked in the excision of the same intron.

摘要

五个属于五个不同互补群的核突变体被证明在五个不同的加工步骤中阻断长形式线粒体cob RNA的成熟。同时,它们阻止了oxi 3 RNA的完全加工,因此表现出线粒体box突变体(细胞色素b -和oxi 3 -)相同的表型。所讨论的不同核因子对从cob RNA中去除内含子具有不同范围的特异性,从仅一个到最多三个内含子。两个突变的核元件被证明对仅存在于长形式cob基因中的内含子的加工具有特异性。正如预期的那样,一种这样的突变对通过细胞导入交换到突变体中的短形式cob RNA的加工没有有害影响。针对两个突变体讨论了核编码因子在内含子编码产物(“成熟酶”)可能的翻译或活性中的作用。在阻断相同内含子切除的pet -和mit -突变体中,在可能从积累的cob RNA中间体翻译的不同多肽产物之间发现了惊人的相似之处。

相似文献

1
Expression of the "split gene" cob in yeast mtDNA. Nuclear mutations specifically block the excision of different introns from its primary transcript.酵母线粒体DNA中“断裂基因” cob 的表达。核突变特异性地阻断了其初级转录本中不同内含子的切除。
J Biol Chem. 1983 Jul 10;258(13):7954-9.
2
Pathways of transcript splicing in yeast mitochondria. Mutations in intervening sequences of the split gene COB reveal a requirement for intervening sequence-encoded products.酵母线粒体中转录剪接的途径。分裂基因COB的间隔序列中的突变揭示了对间隔序列编码产物的需求。
J Biol Chem. 1981 Jul 25;256(14):7610-9.
3
Mutations affecting RNA splicing and the interaction of gene expression of the yeast mitochondrial loci cob and oxi-3.影响酵母线粒体基因座cob和oxi - 3的RNA剪接及基因表达相互作用的突变
Cell. 1980 May;20(1):173-83. doi: 10.1016/0092-8674(80)90245-7.
4
Functional domains in introns. RNA processing intermediates in cis- and trans-acting mutants in the penultimate intron of the mitochondrial gene for cytochrome b.内含子中的功能结构域。细胞色素b线粒体基因倒数第二个内含子顺式和反式作用突变体中的RNA加工中间体。
J Biol Chem. 1983 Feb 10;258(3):1991-9.
5
Two yeast nuclear genes, CBS1 and CBS2, are required for translation of mitochondrial transcripts bearing the 5'-untranslated COB leader.两个酵母核基因CBS1和CBS2是带有5'-非翻译COB前导序列的线粒体转录本翻译所必需的。
Curr Genet. 1986;11(1):41-5. doi: 10.1007/BF00389424.
6
Molecular basis of the 'box effect', A maturase deficiency leading to the absence of splicing of two introns located in two split genes of yeast mitochondrial DNA.“盒效应”的分子基础,一种成熟酶缺陷导致酵母线粒体DNA两个分裂基因中两个内含子缺失剪接。
Eur J Biochem. 1984 Oct 1;144(1):85-93. doi: 10.1111/j.1432-1033.1984.tb08434.x.
7
Leakiness of termination codons in mitochondrial mutants of the yeast Saccharomyces cerevisiae.酿酒酵母线粒体突变体中终止密码子的通读现象。
Mol Gen Genet. 1984;198(2):62-8. doi: 10.1007/BF00328702.
8
Deletions in the cob gene of yeast mtDNA and their phenotypic effect.酵母线粒体DNA中cob基因的缺失及其表型效应。
Curr Genet. 1985;10(4):283-90. doi: 10.1007/BF00365624.
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COX24 codes for a mitochondrial protein required for processing of the COX1 transcript.COX24编码一种处理COX1转录本所需的线粒体蛋白。
J Biol Chem. 2006 Feb 10;281(6):3743-51. doi: 10.1074/jbc.M510778200. Epub 2005 Dec 8.
10
Cloning of a nuclear gene MRS1 involved in the excision of a single group I intron (bI3) from the mitochondrial COB transcript in S. cerevisiae.克隆酿酒酵母中参与从线粒体COB转录本切除单个I组内含子(bI3)的核基因MRS1。
Curr Genet. 1986;11(3):185-91. doi: 10.1007/BF00420605.

引用本文的文献

1
In vivo analysis of sequences required for translation of cytochrome b transcripts in yeast mitochondria.酵母线粒体中细胞色素b转录本翻译所需序列的体内分析。
Mol Cell Biol. 1995 Feb;15(2):780-9. doi: 10.1128/MCB.15.2.780.
2
Leakiness of termination codons in mitochondrial mutants of the yeast Saccharomyces cerevisiae.酿酒酵母线粒体突变体中终止密码子的通读现象。
Mol Gen Genet. 1984;198(2):62-8. doi: 10.1007/BF00328702.
3
Molecular cloning and genetic mapping of the PET494 gene of Saccharomyces cerevisiae.酿酒酵母PET494基因的分子克隆与遗传定位
Mol Gen Genet. 1984;195(1-2):275-80. doi: 10.1007/BF00332759.
4
Mitochondrial suppression of a yeast nuclear mutation which affects the translation of the mitochondrial apocytochrome b transcript.线粒体对酵母核突变的抑制作用,该核突变影响线粒体脱辅基细胞色素b转录本的翻译。
Curr Genet. 1985;9(8):641-8. doi: 10.1007/BF00449816.
5
Mitochondrial protein synthesis is required for maintenance of intact mitochondrial genomes in Saccharomyces cerevisiae.线粒体蛋白质合成对于酿酒酵母中完整线粒体基因组的维持是必需的。
EMBO J. 1985 Aug;4(8):2087-92. doi: 10.1002/j.1460-2075.1985.tb03896.x.
6
Two yeast nuclear genes, CBS1 and CBS2, are required for translation of mitochondrial transcripts bearing the 5'-untranslated COB leader.两个酵母核基因CBS1和CBS2是带有5'-非翻译COB前导序列的线粒体转录本翻译所必需的。
Curr Genet. 1986;11(1):41-5. doi: 10.1007/BF00389424.
7
Product of Saccharomyces cerevisiae nuclear gene PET494 activates translation of a specific mitochondrial mRNA.酿酒酵母核基因PET494的产物可激活特定线粒体mRNA的翻译。
Mol Cell Biol. 1986 Nov;6(11):3694-703. doi: 10.1128/mcb.6.11.3694-3703.1986.
8
Yeast nuclear gene CBS2, required for translational activation of cytochrome b, encodes a basic protein of 45 kDa.酵母核基因CBS2是细胞色素b翻译激活所必需的,它编码一种45 kDa的碱性蛋白。
Mol Gen Genet. 1988 Oct;214(2):263-70. doi: 10.1007/BF00337720.
9
Autocatalytic activities of intron 5 of the cob gene of yeast mitochondria.酵母线粒体cob基因内含子5的自催化活性
Mol Cell Biol. 1988 Jun;8(6):2562-71. doi: 10.1128/mcb.8.6.2562-2571.1988.
10
Three suppressor mutations which cure a mitochondrial RNA maturase deficiency occur at the same codon in the open reading frame of the nuclear NAM2 gene.三种可治愈线粒体RNA成熟酶缺陷的抑制突变发生在核NAM2基因开放阅读框的同一密码子处。
EMBO J. 1987 Mar;6(3):713-21. doi: 10.1002/j.1460-2075.1987.tb04812.x.