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粗糙脉孢菌莫里斯维尔和瓦尔库德线粒体质粒中大片段缺失的分析

Analysis of large deletions in the Mauriceville and Varkud mitochondrial plasmids of Neurospora.

作者信息

Akins R A, Lambowitz A M

机构信息

Department of Molecular Genetics, Ohio State University, Columbus 43210.

出版信息

Curr Genet. 1990 Nov;18(4):365-9. doi: 10.1007/BF00318218.

Abstract

The Mauriceville and Varkud mitochondrial plasmids are closely related, closed-circular DNAs (3.6 and 3.7 kb, respectively) that have characteristics of mtDNA introns and retroid elements. Both plasmids contain a 710 amino acid open reading frame (ORF) that encodes an 81 kDa protein having reverse transcriptase activity. Here, we analyzed two mutant plasmids, V5-36 and M3-24, that have undergone relatively large deletions (approximately 0.35 and 0.5 kb, respectively). Both deletions occur downstream of the long ORF in a non-coding region of the plasmids that contains a direct repeat of 160 bp and a cluster of five PstI-palindromes, a repetitive sequence element in Neurospora mtDNA. In V5-36, the deletion end points are at the bases of two hairpin structures that are centered around PstI-palindromes and flank the deleted region. In M3-24, the deletion junction contains an extra T-residue that is not encoded in the plasmid. In both plasmids, the deletion end points do not correspond to homologous or directly repeated sequences of more than one nucleotide, whose pairing could account for the deletion junction. The characteristics of the deletion end points can be accounted for either by illegitimate recombination, possibly following double strand breaks at cruciform structures, or by interruption of reverse transcription followed by reinitiation downstream. The finding that the deletions encompass the 160 bp direct repeat and all five PstI-palindromes indicates that neither are required for propagation of the plasmids and supports the hypothesis that PstI-palindromes are selfish DNA elements that inserted into a nonessential region of the plasmid.

摘要

莫里斯维尔和瓦尔库德线粒体质粒是密切相关的闭环DNA(分别为3.6和3.7 kb),具有线粒体DNA内含子和类反转录病毒元件的特征。两种质粒都包含一个710个氨基酸的开放阅读框(ORF),该阅读框编码一种具有逆转录酶活性的81 kDa蛋白质。在这里,我们分析了两个突变质粒V5 - 36和M3 - 24,它们分别经历了相对较大的缺失(分别约为0.35和0.5 kb)。这两个缺失都发生在质粒非编码区的长ORF下游,该非编码区包含一个160 bp的直接重复序列和一组五个PstI回文序列,这是粗糙脉孢菌线粒体DNA中的一种重复序列元件。在V5 - 36中,缺失端点位于两个发夹结构的碱基处,这两个发夹结构以PstI回文序列为中心,位于缺失区域的两侧。在M3 - 24中,缺失连接处包含一个额外的T残基,该残基在质粒中没有编码。在这两种质粒中,缺失端点都不对应于超过一个核苷酸的同源或直接重复序列,其配对可以解释缺失连接处。缺失端点的特征可以通过非法重组来解释,可能是在十字形结构处发生双链断裂之后,或者是通过逆转录的中断随后在下游重新起始来解释。缺失包含160 bp直接重复序列和所有五个PstI回文序列的发现表明,这些对于质粒的复制都不是必需的,并支持了PstI回文序列是插入到质粒非必需区域的自私DNA元件这一假说。

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