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基因组DNA的基因内串联重复是导致黑腹果蝇f3N突变的原因。

An intragenic tandem duplication of genomic DNA is responsible for the f3N mutation of Drosophila melanogaster.

作者信息

Ishimaru S, Green M M, Saigo K

机构信息

Department of Biophysics and Biochemistry, School of Science, University of Tokyo, Japan.

出版信息

Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2999-3003. doi: 10.1073/pnas.92.7.2999.

Abstract

Among the numerous X chromosome-linked forked bristle (f) mutations described in Drosophila melanogaster, one designated f3N exhibits the unusual property of reverting spontaneously to wild type at an inordinate frequency, a frequency that can be increased with x-ray irradiation. In contrast to the f mutants described thus far, all of which are associated with the insertion of mobile DNA elements, f3N is associated with an intragenic duplication of 2.8 kb of genomic DNA that resolves to the normal sequence when reversions occur. Consideration is given to intrachromosomal recombination as the mechanism of reversion and truncation of the forked protein as a cause for the mutant phenotype.

摘要

在黑腹果蝇中描述的众多X染色体连锁的叉刚毛(f)突变中,一个名为f3N的突变具有不同寻常的特性,即它会以极高的频率自发回复到野生型,而且X射线照射可以提高这种回复频率。与迄今描述的所有f突变体不同,迄今为止描述的所有f突变体都与移动DNA元件的插入有关,而f3N与2.8 kb基因组DNA的基因内重复有关,当发生回复突变时,该重复会恢复为正常序列。研究认为染色体内部重组是回复突变的机制,而叉刚毛蛋白的截短是突变表型的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5c1/42346/00ea9927bd26/pnas01485-0592-a.jpg

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