非编码变化导致近缘的纳氏寡节茧蜂属物种之间出现性别的翅膀大小差异。

Non-coding changes cause sex-specific wing size differences between closely related species of Nasonia.

机构信息

Department of Biology, University of Rochester, Rochester, New York, USA.

出版信息

PLoS Genet. 2010 Jan 15;6(1):e1000821. doi: 10.1371/journal.pgen.1000821.

Abstract

The genetic basis of morphological differences among species is still poorly understood. We investigated the genetic basis of sex-specific differences in wing size between two closely related species of Nasonia by positional cloning a major male-specific locus, wing-size1 (ws1). Male wing size increases by 45% through cell size and cell number changes when the ws1 allele from N. giraulti is backcrossed into a N. vitripennis genetic background. A positional cloning approach was used to fine-scale map the ws1 locus to a 13.5 kilobase region. This region falls between prospero (a transcription factor involved in neurogenesis) and the master sex-determining gene doublesex. It contains the 5'-UTR and cis-regulatory domain of doublesex, and no coding sequence. Wing size reduction correlates with an increase in doublesex expression level that is specific to developing male wings. Our results indicate that non-coding changes are responsible for recent divergence in sex-specific morphology between two closely related species. We have not yet resolved whether wing size evolution at the ws1 locus is caused by regulatory alterations of dsx or prospero, or by another mechanism. This study demonstrates the feasibility of efficient positional cloning of quantitative trait loci (QTL) involved in a broad array of phenotypic differences among Nasonia species.

摘要

物种间形态差异的遗传基础仍知之甚少。我们通过定位克隆一个主要的雄性特异性位点 wing-size1 (ws1),研究了两个近缘种 Nasonia 中翅膀大小的性别特异性差异的遗传基础。当 N. giraulti 的 ws1 等位基因回交到 N. vitripennis 的遗传背景中时,雄蝇的翅膀大小通过细胞大小和细胞数量的变化增加了 45%。我们使用定位克隆方法将 ws1 基因座精细映射到 13.5 千碱基的区域。该区域位于 prospero(参与神经发生的转录因子)和主要性别决定基因 doublesex 之间。它包含 doublesex 的 5'-UTR 和顺式调控区,没有编码序列。翅膀大小的减小与 doublesex 表达水平的增加相关,这种增加是雄性翅膀特有的。我们的结果表明,非编码变化是两个近缘种之间性别特异性形态差异的近期分化的原因。我们尚未确定 ws1 基因座上的翅膀大小进化是由于 dsx 或 prospero 的调控改变,还是由另一种机制引起的。这项研究表明,在 Nasonia 物种之间广泛存在的表型差异中,高效定位克隆数量性状基因座(QTL)是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/360d/2799512/9739eed39d42/pgen.1000821.g001.jpg

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