Conserved and Quickly Evolving Immunome Genes Have Different Evolutionary Paths

被引:2
|
作者
Ortutay, Csaba [2 ,3 ]
Vihinen, Mauno [1 ,2 ,3 ]
机构
[1] Lund Univ, Dept Expt Med Sci, SE-22184 Lund, Sweden
[2] BioMediTech, Tampere, Finland
[3] Univ Tampere, Inst Biomed Technol, FIN-33101 Tampere, Finland
关键词
human immune system; directed genes; conserved genes; animal disease models; MESSENGER-RNA CONCENTRATION; COPY NUMBER VARIATION; DROSOPHILA-MELANOGASTER; NLRP3; INFLAMMASOME; MUTATION DATABASE; CODON USAGE; LENGTH; PROTEINS; REGISTRY; LOCUS;
D O I
10.1002/humu.22125
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic, transcript, and protein level variations have important functional and evolutionary consequences. We performed systematic data collection and analysis of copy-number variations, single-nucleotide polymorphisms, disease-causing variations, messenger RNA splicing variants, and protein posttranslational modifications for the genes and proteins essential for human immune system. Information about polymorphic and evolutionarily fixed genetic variations was used to group immunome genes to the most conserved and the most quickly changing ones under directed selection during the recent immunome evolution. Gene Ontology terms related to adaptive immunity are associated with gene groups subject to recent directing selection. In addition, several other characteristics of the immunome genes and proteins in these two categories have statistically significant differences. The presented findings question the usability of directed mouse genes as models for human diseases and conditions and shed light on the fine tuning of human immunity and its diverse functions. HumMutat 33:1456-1463, 2012. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1456 / 1463
页数:8
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