Not born equal: Increased rate asymmetry in relocated and retrotransposed rodent gene duplicates

被引:79
作者
Cusack, Brian P. [1 ]
Wolfe, Kenneth H. [1 ]
机构
[1] Trinity Coll Dublin, Smurfit Inst Genet, Dublin, Ireland
关键词
retrotransposition; gene duplication; asymmetry;
D O I
10.1093/molbev/msl199
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Duplicated genes frequently evolve at different rates. This asymmetry is evidence of natural selection's ability to discriminate between the 2 copies, subjecting them to different levels of purifying selection or even permitting adaptive evolution of one or both copies. However, if gene duplication creates pairs of protein-coding sequences that are initially identical, this raises the question of how selection tells the 2 copies apart. Here, we investigated asymmetric sequence divergence of recently duplicated genes in rodents and related this to 2 possible sources of such asymmetry: gene relocation as a consequence of duplication and retrotransposition as a mechanism of gene duplication. We found that most young rodent duplicates that have been relocated were created by retrotransposition. The degree of rate asymmetry in gene pairs where one copy has been relocated (either by retrotransposition or DNA-based duplication) is greater than in pairs formed by local DNA-based duplication events. Furthermore, by considering the direction of transposition for distant duplicates, we found a consistent tendency for retrogenes to undergo accelerated protein evolution relative to their static paralogs, whereas DNA-based transpositions showed no such tendency. Finally, we demonstrate that the faster sequence evolution of retrogenes correlates with the profound alteration of their expression pattern that is precipitated by retrotransposition.
引用
收藏
页码:679 / 686
页数:8
相关论文
共 35 条
[21]   Correlation between sequence conservation and the genomic context after gene duplication [J].
Notebaart, RA ;
Huynen, MA ;
Teusink, B ;
Siezen, RJ ;
Snel, B .
NUCLEIC ACIDS RESEARCH, 2005, 33 (19) :6164-6171
[22]  
Pál C, 2001, GENETICS, V158, P927
[23]   Evolutionary origin and maintenance of coexpressed gene clusters in mammals [J].
Semon, Marie ;
Duret, Laurent .
MOLECULAR BIOLOGY AND EVOLUTION, 2006, 23 (09) :1715-1723
[24]   Clusters of co-expressed genes in mammalian genomes are conserved by natural selection [J].
Singer, GAC ;
Lloyd, AT ;
Huminiecki, LB ;
Wolfe, KH .
MOLECULAR BIOLOGY AND EVOLUTION, 2005, 22 (03) :767-775
[25]   TissueInfo: high-throughput identification of tissue expression profiles and specificity [J].
Skrabanek, L ;
Campagne, F .
NUCLEIC ACIDS RESEARCH, 2001, 29 (21)
[26]   RNA-MEDIATED GENE DUPLICATION - THE RAT PREPROINSULIN-I GENE IS A FUNCTIONAL RETROPOSON [J].
SOARES, MB ;
SCHON, E ;
HENDERSON, A ;
KARATHANASIS, SK ;
CATE, R ;
ZEITLIN, S ;
CHIRGWIN, J ;
EFSTRATIADIS, A .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (08) :2090-2103
[27]  
Spellman Paul T, 2002, J Biol, V1, P5, DOI 10.1186/1475-4924-1-5
[28]   Gene expression intensity shapes evolutionary rates of the proteins encoded by the vertebrate genome [J].
Subramanian, S ;
Kumar, S .
GENETICS, 2004, 168 (01) :373-381
[29]  
Susumu O., 1970, EVOLUTION GENE DUPLI
[30]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680