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AAR2,一种在酿酒酵母细胞类型控制中参与MATa1顺反子前体mRNA剪接的基因。

AAR2, a gene for splicing pre-mRNA of the MATa1 cistron in cell type control of Saccharomyces cerevisiae.

作者信息

Nakazawa N, Harashima S, Oshima Y

机构信息

Department of Biotechnology, Faculty of Engineering, Osaka University, Japan.

出版信息

Mol Cell Biol. 1991 Nov;11(11):5693-700. doi: 10.1128/mcb.11.11.5693-5700.1991.

Abstract

We have isolated a class of mutants, aar2, showing the alpha mating type due to a defect in a1-alpha 2 repression but with alpha 2 repression activity from a nonmater strain of Saccharomyces cerevisiae expressing both a and alpha mating-type information in duplicate. Cells of the aar2 mutant and the aar2 disruptant also show a growth defect. A DNA fragment complementing the aar2 mutation contains an open reading frame consisting of 355 amino acid codons. Northern hybridization showed that cells of the aar2 mutant and disruptant contained alpha 1 and alpha 2 transcripts of the MAT alpha gene (or HML alpha in sir3 cells), but their a1 transcript of MATa (or HMRa in sir3 cells) migrated more slowly than that of the wild-type cells on gel electrophoresis and gave a diffused band. Primer extension analysis showed that the aar2 mutant and disruptant have a defect in splicing two short introns of the a1 pre-mRNA but not in splicing pre-mRNA of ACT1. The alpha mating type, but not the slow-growing phenotype, of the aar2 mutant was suppressed by introduction of an intronless MATa1 DNA. Thus, the AAR2 gene is involved in splicing pre-mRNA of the a1 cistron and other genes that are important for cell growth. The AAR2 locus was mapped on chromosome II beside the SSA3 locus, with a 276-bp space, but was not allelic to either PRP5 or PRP6, which are both located on chromosome II and function in splicing pre-mRNA of ACT1.

摘要

我们从酿酒酵母的一个非亲株中分离出了一类突变体aar2,该菌株在重复表达a和α交配型信息时,由于a1-α2抑制缺陷而表现出α交配型,但具有α2抑制活性。aar2突变体和aar2缺失体的细胞也表现出生长缺陷。一个能互补aar2突变的DNA片段包含一个由355个氨基酸密码子组成的开放阅读框。Northern杂交显示,aar2突变体和缺失体的细胞含有MATα基因(或sir3细胞中的HMLα)的α1和α2转录本,但它们的MATa(或sir3细胞中的HMRa)的a1转录本在凝胶电泳上的迁移速度比野生型细胞的慢,并且呈现出弥散条带。引物延伸分析表明,aar2突变体和缺失体在剪接a1前体mRNA的两个短内含子时存在缺陷,但在剪接ACT1的前体mRNA时没有缺陷。通过导入无内含子的MATa1 DNA可抑制aar2突变体的α交配型,但不能抑制其生长缓慢的表型。因此,AAR2基因参与a1顺反子的前体mRNA剪接以及其他对细胞生长重要的基因的剪接。AAR2基因座位于II号染色体上SSA3基因座旁边,间隔276 bp,但与同样位于II号染色体上且在剪接ACT1前体mRNA中起作用的PRP5或PRP6均不等位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1710/361940/c36e706e8e2d/molcellb00035-0321-a.jpg

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