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丽蝇(Phormia regina)的线粒体DNA:限制性分析和基因定位

Mitochondrial DNA of the blowfly Phormia regina: restriction analysis and gene localization.

作者信息

Goldenthal M J, McKenna K A, Joslyn D J

机构信息

Department of Biology, Rutgers University, Camden, New Jersey 08102.

出版信息

Biochem Genet. 1991 Feb;29(1-2):1-11. doi: 10.1007/BF00578235.

Abstract

A study of an invertebrate mitochondrial genome, that of the blowfly Phormia regina, has been initiated to compare its structural and functional relatedness to other metazoan mitochondrial genomes. A restriction map of mitochondrial DNA (mtDNA) isolated from sucrose gradient-purified mitochondria has been established using a combination of single and double restriction endonuclease digestions and hybridizations with isolated mtDNA fragments, revealing a genome size of 17.5 kilobases (kb). A number of mitochondrial genes including those encoding the 12 S and 16 S ribosomal RNA, the cytochrome c oxidase I subunit (COI) and an unidentified open reading frame (URF2) have been located on the Phormia mtDNA by Southern blot analysis using as probes both isolated mtDNA fragments and oligonucleotides derived from the sequences of previously characterized genes from rat and Drosophila yakuba mtDNAs. These data indicate that for those regions examined, the mitochondrial genome organization of blowfly mtDNA is the same as that of Drosophila yakuba, the order being COI-URF2-12 S-16 S. These data also report the presence of an A + T-rich region, located as a 2.5-kb region between the URF2 and the 12 S rRNA genes, and its amplification by the polymerase chain reaction is described.

摘要

一项关于无脊椎动物线粒体基因组(即丽蝇伏蝇的线粒体基因组)的研究已经启动,目的是比较其与其他后生动物线粒体基因组在结构和功能上的相关性。通过单酶切和双酶切以及与分离的线粒体DNA片段杂交相结合的方法,构建了从蔗糖梯度纯化的线粒体中分离出的线粒体DNA(mtDNA)的限制酶图谱,结果显示基因组大小为17.5千碱基(kb)。利用分离的线粒体DNA片段和从大鼠及雅库布果蝇线粒体DNA中先前已鉴定基因的序列衍生而来的寡核苷酸作为探针,通过Southern印迹分析,在丽蝇线粒体DNA上定位了多个线粒体基因,包括编码12S和16S核糖体RNA、细胞色素c氧化酶I亚基(COI)以及一个未鉴定的开放阅读框(URF2)的基因。这些数据表明,在所检测的区域中,丽蝇线粒体DNA的线粒体基因组组织与雅库布果蝇相同,顺序为COI - URF2 - 12S - 16S。这些数据还报告了一个富含A + T的区域的存在,该区域位于URF2和12S rRNA基因之间,大小为2.5 kb,并描述了通过聚合酶链反应对其进行扩增的情况。

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