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酵母线粒体DNA中富含G + C的移动簇的假定靶位点:单个元件和串联阵列。

Putative target sites for mobile G + C rich clusters in yeast mitochondrial DNA: single elements and tandem arrays.

作者信息

Weiller G, Schueller C M, Schweyen R J

机构信息

Institut für Genetik und Mikrobiologie, Universität München, Federal Republic of Germany.

出版信息

Mol Gen Genet. 1989 Aug;218(2):272-83. doi: 10.1007/BF00331278.

Abstract

GC clusters constitute the major repetitive elements in the mitochondrial (mt) genome of the yeast Saccharomyces cerevisiae. Many of these clusters are optional and thus contribute much to the polymorphism of yeast mtDNAs. We have made a systematic search for polymorphic sites by comparing mtDNA sequences of various yeast strains. Most of the 26 di- or polymorphic sites found differ by the presence or absence of a GC cluster of the majority class, here referred to as the M class, which terminate with an AGGAG motif. Comparison of sequences with and without the GC clusters reveal that elements of the subclasses M1 and M2 are inserted 3' to a TAG, flanked by A + T rich sequences. M3 elements, in contrast, only occur in tandem arrays of two to four GC clusters; they are consistently inserted 3' to the AGGAG terminal sequence of a preexisting cluster. The TAG or the terminal AGGAG, therefore, are regarded as being part of the target sites for M1 and M2 or M3 elements, respectively. The dinucleotide AG is in common to both target sites; it also occurs at the 3' terminus (AGGAG). This suggests its duplication during GC cluster insertion. This notion is supported by the observation that GC clusters of the minor classes G and V similarily repeat at their 3' terminus a GT or an AA dinucleotide, respectively, from their putative target sites.

摘要

GC簇构成了酿酒酵母线粒体(mt)基因组中的主要重复元件。这些簇中的许多是可有可无的,因此对酵母线粒体DNA的多态性有很大贡献。我们通过比较各种酵母菌株的线粒体DNA序列,系统地搜索了多态性位点。发现的26个双态或多态性位点中的大多数,其差异在于是否存在多数类型的GC簇,这里称为M类,其以AGGAG基序结尾。对有和没有GC簇的序列进行比较发现,M1和M2亚类的元件插入到TAG的3'端,两侧是富含A + T的序列。相比之下,M3元件仅以两到四个GC簇的串联阵列形式出现;它们始终插入到预先存在的簇的AGGAG末端序列的3'端。因此,TAG或末端AGGAG分别被视为M1和M2或M3元件靶位点的一部分。双核苷酸AG在两个靶位点中都有;它也出现在3'末端(AGGAG)。这表明它在GC簇插入过程中发生了重复。这一观点得到了以下观察结果的支持:较小的G类和V类GC簇分别在其3'末端重复来自其假定靶位点的GT或AA双核苷酸。

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