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从海德果蝇Y染色体灯刷环“细丝”显微切割得到的微小P元件长末端重复序列的特征分析。

Characterization of the long terminal repeats of micropia elements microdissected from the Y-chromosomal lampbrush loops "threads" of Drosophila hydei.

作者信息

Lankenau D H, Huijser P, Hennig W

机构信息

Department of Molecular and Developmental Genetics, University of Nijmegen, The Netherlands.

出版信息

J Mol Biol. 1989 Oct 5;209(3):493-7. doi: 10.1016/0022-2836(89)90013-2.

Abstract

Four micropia elements from Drosophila melanogaster and D. hydei have been analysed by sequencing. Two elements, from D. hydei, micropia-DhMiF8 and -DhMiF2, were recovered by cloning microdissected Y-chromosomal lampbrush loops "threads". This method allows isolation of repetitive sequences from defined chromosomal positions, but recovery of large and overlapping inserts is difficult. In case of the Y-chromosomal micropia elements it was not possible to define the endpoints of their long terminal repeat sequences precisely. Comparison of these locus-defined micropia elements to complete micropia elements isolated from D. melanogaster allowed identification of micropia-DhMiF8 and micropia-DhMiF2 long terminal repeats (LTRs). LTR sequences from the two Drosophila species are not conserved except for a few short sequences found at comparable positions that are believed to have functional significance. In contrast, the Leu-tRNA primer binding site and plus strand primer binding site are conserved between D. melanogaster and D. hydei.

摘要

通过测序分析了黑腹果蝇和海德氏果蝇的四个微小病毒元件。从海德氏果蝇中获得了两个元件,微小病毒-DhMiF8和-DhMiF2,它们是通过克隆显微切割的Y染色体灯刷环“细丝”回收的。这种方法允许从特定染色体位置分离重复序列,但难以回收大的和重叠的插入片段。对于Y染色体微小病毒元件,无法精确确定其长末端重复序列的端点。将这些位点定义的微小病毒元件与从黑腹果蝇中分离出的完整微小病毒元件进行比较,从而鉴定出微小病毒-DhMiF8和微小病毒-DhMiF2的长末端重复序列(LTR)。除了在可比位置发现的一些被认为具有功能意义的短序列外,这两种果蝇物种的LTR序列并不保守。相比之下,黑腹果蝇和海德氏果蝇之间的亮氨酸-tRNA引物结合位点和正链引物结合位点是保守的。

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