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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。

Functional domains in introns. RNA processing intermediates in cis- and trans-acting mutants in the penultimate intron of the mitochondrial gene for cytochrome b.

作者信息

Lamb M R, Anziano P Q, Glaus K R, Hanson D K, Klapper H J, Perlman P S, Mahler H R

出版信息

J Biol Chem. 1983 Feb 10;258(3):1991-9.

PMID:6296117
Abstract

The penultimate intron of the split mitochondrial gene (cob) for apocytochrome b of Saccharomyces cerevisiae is of particular interest; it contains a long unassigned reading frame, is present in both long form (six exons) and short form (three exons) of the gene, and a product expressed from it is required for the removal of its transcript and that of an intron in the transcript of the oxi3 gene. Complementation analysis shows mutants in this intron to be either cis-dominant or transrecessive. Cis-dominant mutants are located in the first third (approximately 350 base pairs) of the open and near the 3'-end of the closed reading frame, while trans-recessive mutants are scattered throughout the remaining two-thirds (approximately 750 base pairs) of the open frame. Mutants in both classes exhibit the same pattern of splicing defects in their transcripts, but for different reasons. Those in the trans-recessive class lack a functional maturase (probably a protein of Mr = 27,000) encoded wholly within the 3'-terminal segment of the intron, and for this reason also fail to express oxi3. In contrast, cis-dominant mutants are incapable of providing the splicing complex with a substrate of appropriate 2 degrees structure. They also accumulate a novel transcript, 1900 nucleotides long, which contains the intron fused to the downstream (3') exons. This may reflect an inability of the splicing complex to complete the normal sequence of cleavage of the intron at its downstream junction and the ligation of the two exonic moieties.

摘要

酿酒酵母脱辅基细胞色素b的线粒体分裂基因(cob)的倒数第二个内含子特别引人关注;它包含一个长的未指定阅读框,存在于该基因的长形式(六个外显子)和短形式(三个外显子)中,并且其转录本以及oxi3基因转录本中的一个内含子的去除需要由它表达的产物。互补分析表明,该内含子中的突变体要么是顺式显性的,要么是反式隐性的。顺式显性突变体位于开放阅读框的前三分之一(约350个碱基对)且靠近封闭阅读框的3'端,而反式隐性突变体则分散在开放阅读框其余的三分之二(约750个碱基对)中。两类突变体在其转录本中表现出相同的剪接缺陷模式,但原因不同。反式隐性类中的突变体缺乏完全在内含子3'末端区段编码的功能性成熟酶(可能是一个分子量为27,000的蛋白质),因此也无法表达oxi3。相反,顺式显性突变体无法为剪接复合体提供具有适当二级结构的底物。它们还积累了一种新的转录本,长度为1900个核苷酸,其中包含与下游(3')外显子融合的内含子。这可能反映了剪接复合体无法完成内含子在其下游连接处的正常切割序列以及两个外显子部分的连接。

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