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触角足显性同源异形表型的分子分析。

Molecular analysis of the dominant homeotic Antennapedia phenotype.

机构信息

Department of Cell Biology, Biozentrum, University of Basel, Klingelbergstrasse 70, CH-4056 Basel, Switzerland.

出版信息

EMBO J. 1987 Jan;6(1):201-6. doi: 10.1002/j.1460-2075.1987.tb04739.x.

Abstract

Most of the dominant alleles of the homeotic gene Antennapedia (Antp) which show a transformation of antennae into legs are associated with large chromosomal inversions. To determine the molecular mechanisms underlying the dominant phenotype, one of the strongest Antp alleles (Antp) was studied in more detail. The mutant chromosome has been cloned and the structure of the inversion has been identified. The inversion breaks two genes apart: the Antp gene and a previously unidentified gene, tentatively called responsible for dominant phenotype (rfd), located at 84D1-2. The two genes are transcribed in opposite directions and the breakpoints lie within introns of both genes. Through the inversion event, a reciprocal exchange of the first exons including promoters occurred leading to the production of new transcripts. The transcripts containing the entire Antp protein coding region which have been fused to the promoter of the rfd gene are lost in revertants of the dominant phenotype indicating a correlation between this fusion gene and the dominant phenotype. The molecular structure of inversion Antp suggests that the dominant phenotype arises via ectopic expression of the normal Antp protein due to a gene fusion event.

摘要

大多数具有触角转变成腿的显性等位基因 Antennapedia(Antp)与大的染色体倒位有关。为了确定显性表型的分子机制,对最强的 Antp 等位基因(Antp)之一进行了更详细的研究。已经克隆了突变染色体,并且鉴定了倒位的结构。该倒位将两个基因分开:Antp 基因和一个先前未识别的基因,暂时称为负责显性表型的基因(rfd),位于 84D1-2。这两个基因以相反的方向转录,断裂点位于两个基因的内含子内。通过倒位事件,发生了第一个外显子的相互交换,包括启动子,导致新转录物的产生。含有整个 Antp 蛋白编码区的转录本与 rfd 基因的启动子融合,在显性表型的回复突变体中丢失,表明这种融合基因与显性表型之间存在相关性。倒位 Antp 的分子结构表明,由于基因融合事件,正常 Antp 蛋白的异位表达导致了显性表型的出现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ac/553377/9d39f42bcd6f/emboj00241-0199-a.jpg

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