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剑尾鱼属鱼类中DAB和DXB MHC II类基因座的不同选择模式。

Divergent patterns of selection on the DAB and DXB MHC class II loci in Xiphophorus fishes.

作者信息

Summers Kyle, Roney Kelly E, da Silva Jack, Capraro Gerald, Cuthbertson Brandon J, Kazianis Steven, Rosenthal Gil G, Ryan Michael J, McConnell Thomas J

机构信息

Department of Biology, East Carolina University, Greenville, NC 27858, USA.

出版信息

Genetica. 2009 Apr;135(3):379-90. doi: 10.1007/s10709-008-9284-4. Epub 2008 Jul 4.

Abstract

Two MHC class II loci, DAB (a classical class II locus) and DXB (putatively a non-classical class II locus), were sequenced in samples of individuals from two populations of swordtail fish, Xiphophorus multilineatus and X. pygmaeus. The DAB locus showed higher levels of genetic variation in the B1-encoding region, (putative binding region) than the DXB locus. We used two methods to investigate d(N)/d(S) ratios. The results from a maximum likelihood method based on phylogenetic relationships indicated positive selection on the B1 region of DAB (this method could not be used on DXB). Results from a coalescent-based method also showed evidence for positive selection in the B1 region of DAB, but only weak evidence for selection on the DXB. Further analyses indicated that recombination is an important source of variation in the B1 region of DAB, but has a relatively small effect on DXB. Overall, our results were consistent with the hypothesis that the DAB locus is under positive selection driven by antagonistic coevolution, and that the DXB locus plays the role of a non-classical MHC II locus. We also used simulations to investigate the presence of an elevated synonymous substitution rate in the binding region. The simulations revealed that the elevated rate could be caused by an interaction between positive selection and codon bias.

摘要

在剑尾鱼(Xiphophorus multilineatus和X. pygmaeus)两个种群的个体样本中,对两个MHC II类基因座DAB(一个经典的II类基因座)和DXB(推测为非经典的II类基因座)进行了测序。DAB基因座在B1编码区(推测的结合区)显示出比DXB基因座更高水平的遗传变异。我们使用两种方法来研究d(N)/d(S)比率。基于系统发育关系的最大似然法结果表明,DAB的B1区域受到正选择(该方法不能用于DXB)。基于合并的方法结果也显示DAB的B1区域有正选择的证据,但DXB上只有微弱的选择证据。进一步分析表明,重组是DAB的B1区域变异的重要来源,但对DXB的影响相对较小。总体而言,我们的结果与以下假设一致:DAB基因座受到拮抗协同进化驱动的正选择,而DXB基因座发挥非经典MHC II类基因座的作用。我们还使用模拟来研究结合区同义替换率升高的情况。模拟结果显示,升高的比率可能是由正选择和密码子偏好之间的相互作用引起的。

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