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猕猴亚种间氨基酸序列直系同源物的进化距离:鉴定中国恒河猴中抗猴免疫缺陷病毒的候选基因。

Evolutionary distance of amino acid sequence orthologs across macaque subspecies: identifying candidate genes for SIV resistance in Chinese rhesus macaques.

作者信息

Ross Cody T, Roodgar Morteza, Smith David Glenn

机构信息

Department of Anthropology, University of California, Davis. Davis, United States of America; Molecular Anthropology Laboratory, University of California, Davis. Davis, United States of America.

Molecular Anthropology Laboratory, University of California, Davis. Davis, United States of America; California National Primate Research Center, University of California, Davis. Davis, United States of America; Graduate Group of Comparative Pathology, University of California, Davis. Davis, United States of America.

出版信息

PLoS One. 2015 Apr 17;10(4):e0123624. doi: 10.1371/journal.pone.0123624. eCollection 2015.

Abstract

We use the Reciprocal Smallest Distance (RSD) algorithm to identify amino acid sequence orthologs in the Chinese and Indian rhesus macaque draft sequences and estimate the evolutionary distance between such orthologs. We then use GOanna to map gene function annotations and human gene identifiers to the rhesus macaque amino acid sequences. We conclude methodologically by cross-tabulating a list of amino acid orthologs with large divergence scores with a list of genes known to be involved in SIV or HIV pathogenesis. We find that many of the amino acid sequences with large evolutionary divergence scores, as calculated by the RSD algorithm, have been shown to be related to HIV pathogenesis in previous laboratory studies. Four of the strongest candidate genes for SIVmac resistance in Chinese rhesus macaques identified in this study are CDK9, CXCL12, TRIM21, and TRIM32. Additionally, ANKRD30A, CTSZ, GORASP2, GTF2H1, IL13RA1, MUC16, NMDAR1, Notch1, NT5M, PDCD5, RAD50, and TM9SF2 were identified as possible candidates, among others. We failed to find many laboratory experiments contrasting the effects of Indian and Chinese orthologs at these sites on SIVmac pathogenesis, but future comparative studies might hold fertile ground for research into the biological mechanisms underlying innate resistance to SIVmac in Chinese rhesus macaques.

摘要

我们使用倒数最小距离(RSD)算法来识别中国恒河猴和印度恒河猴草图序列中的氨基酸序列直系同源物,并估计这些直系同源物之间的进化距离。然后,我们使用GOanna将基因功能注释和人类基因标识符映射到恒河猴氨基酸序列上。我们通过将具有大差异得分的氨基酸直系同源物列表与已知参与SIV或HIV发病机制的基因列表进行交叉制表,从方法学上得出结论。我们发现,根据RSD算法计算,许多具有大进化差异得分的氨基酸序列在先前的实验室研究中已被证明与HIV发病机制有关。本研究中确定的中国恒河猴中对SIVmac抗性最强的四个候选基因是CDK9、CXCL12、TRIM21和TRIM32。此外,ANKRD30A、CTSZ、GORASP2、GTF2H1、IL13RA1、MUC16、NMDAR1、Notch1、NT5M、PDCD5、RAD50和TM9SF2等也被确定为可能的候选基因。我们未能找到许多对比这些位点上印度和中国直系同源物对SIVmac发病机制影响的实验室实验,但未来的比较研究可能为研究中国恒河猴对SIVmac先天抗性背后的生物学机制提供丰富的研究素材。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5236/4401517/230822fd07ab/pone.0123624.g001.jpg

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