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本文引用的文献

1
Mega2: data-handling for facilitating genetic linkage and association analyses.Mega2:用于促进基因连锁和关联分析的数据处理
Bioinformatics. 2005 May 15;21(10):2556-7. doi: 10.1093/bioinformatics/bti364. Epub 2005 Mar 3.
2
Molecular evolution meets the genomics revolution.分子进化遇上基因组学革命。
Nat Genet. 2003 Mar;33 Suppl:255-65. doi: 10.1038/ng1088.
3
Splitting pairs: the diverging fates of duplicated genes.基因对的分化:重复基因的不同命运
Nat Rev Genet. 2002 Nov;3(11):827-37. doi: 10.1038/nrg928.
4
Simulation study of the reliability and robustness of the statistical methods for detecting positive selection at single amino acid sites.检测单个氨基酸位点正选择的统计方法的可靠性和稳健性的模拟研究
Mol Biol Evol. 2002 Nov;19(11):1865-9. doi: 10.1093/oxfordjournals.molbev.a004010.
5
Detecting recent positive selection in the human genome from haplotype structure.从单倍型结构检测人类基因组中近期的正选择。
Nature. 2002 Oct 24;419(6909):832-7. doi: 10.1038/nature01140. Epub 2002 Oct 9.
6
Orphan G protein-coupled receptors MrgA1 and MrgC11 are distinctively activated by RF-amide-related peptides through the Galpha q/11 pathway.孤儿G蛋白偶联受体MrgA1和MrgC11通过Gαq/11途径被RF酰胺相关肽特异性激活。
Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14740-5. doi: 10.1073/pnas.192565799. Epub 2002 Oct 23.
7
Duplication and adaptive evolution of the chalcone synthase genes of Dendranthema (Asteraceae).菊属(菊科)查尔酮合酶基因的复制与适应性进化
Mol Biol Evol. 2002 Oct;19(10):1752-9. doi: 10.1093/oxfordjournals.molbev.a003997.
8
Molecular evolution of FOXP2, a gene involved in speech and language.FOXP2基因的分子进化,该基因与言语和语言有关。
Nature. 2002 Aug 22;418(6900):869-72. doi: 10.1038/nature01025. Epub 2002 Aug 14.
9
Ratios of radical to conservative amino acid replacement are affected by mutational and compositional factors and may not be indicative of positive Darwinian selection.激进氨基酸替换与保守氨基酸替换的比率受突变和组成因素影响,可能并不表明存在正达尔文选择。
Mol Biol Evol. 2002 Jul;19(7):1022-5. doi: 10.1093/oxfordjournals.molbev.a004161.
10
Adaptive evolution of a duplicated pancreatic ribonuclease gene in a leaf-eating monkey.食叶猴中一个重复的胰腺核糖核酸酶基因的适应性进化。
Nat Genet. 2002 Apr;30(4):411-5. doi: 10.1038/ng852. Epub 2002 Mar 4.

MRG的适应性进化,MRG是一个与痛觉感受相关的神经元特异性基因家族。

Adaptive evolution of MRG, a neuron-specific gene family implicated in nociception.

作者信息

Choi Sun Shim, Lahn Bruce T

机构信息

Howard Hughes Medical Institute and Department of Human Genetics, University of Chicago, Chicago, Illinois 60637, USA.

出版信息

Genome Res. 2003 Oct;13(10):2252-9. doi: 10.1101/gr.1431603.

DOI:10.1101/gr.1431603
PMID:14525927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC403691/
Abstract

The MRG gene family (also known as SNSR) belongs to the G-protein-coupled receptor (GPCR) superfamily, is expressed specifically in nociceptive neurons, and is implicated in the modulation of nociception. Here, we show that Ka/Ks (the ratio between nonsynonymous and synonymous substitution rates) displays distinct profiles along the coding regions of MRG, with peaks (Ka/Ks>1) corresponding to extracellular domains, and valleys (Ka/Ks<1) corresponding to transmembrane and cytoplasmic domains. The extracellular domains are also characterized by a significant excess of radical amino acid changes. Statistical analysis shows that positive selection is by far the most suitable model to account for the nucleotide substitution patterns in MRG. Together, these results demonstrate that the extracellular domains of the MRG receptor family, which presumably partake in ligand binding, have experienced strong positive selection. Such selection is likely directed at altering the sensitivity and/or selectivity of nociceptive neurons to aversive stimuli. Thus, our finding suggests pain perception as an aspect of the nervous system that may have experienced a surprising level of adaptive evolution.

摘要

MRG基因家族(也称为SNSR)属于G蛋白偶联受体(GPCR)超家族,在伤害性神经元中特异性表达,并参与伤害感受的调节。在此,我们表明Ka/Ks(非同义替换率与同义替换率之比)在MRG的编码区域呈现出不同的分布特征,峰值(Ka/Ks>1)对应于细胞外结构域,谷值(Ka/Ks<1)对应于跨膜和细胞质结构域。细胞外结构域还具有明显过量的激进氨基酸变化。统计分析表明,正选择是迄今为止解释MRG中核苷酸替换模式的最合适模型。总之,这些结果表明,可能参与配体结合的MRG受体家族的细胞外结构域经历了强烈的正选择。这种选择可能旨在改变伤害性神经元对厌恶刺激的敏感性和/或选择性。因此,我们的发现表明疼痛感知是神经系统中可能经历了惊人程度适应性进化的一个方面。