Selective Constraint on Copy Number Variation in Human Piwi-Interacting RNA Loci

被引:5
|
作者
Gould, David W.
Lukic, Sergio
Chen, Kevin C. [1 ]
机构
[1] Rutgers State Univ, BioMaPS Inst Quantitat Biol, Piscataway, NJ 08855 USA
来源
PLOS ONE | 2012年 / 7卷 / 10期
基金
美国国家卫生研究院;
关键词
PIRNA CLUSTERS; HUMAN GENOME; DROSOPHILA; ALIGNMENT; EVOLUTION; MICRORNAS;
D O I
10.1371/journal.pone.0046611
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Piwi-interacting RNAs (piRNAs) are a recently discovered class of small non-coding RNA found in animals. PiRNAs are primarily expressed in the germline where their best understood function is to repress transposable elements. Unlike previous studies that investigated the evolution of piRNA-generating loci at the level of nucleotide substitutions, here we studied the evolution of piRNA-generating loci at the level of copy number variation (i.e. duplications and deletions) using genome-wide copy number variation data from three human populations. Our analysis shows that at the level of copy number variation there is strong selective constraint and a very high mutation rate in human piRNA-generating loci. Our results differ from a model of positive selection on copy number variation in piRNA-generating loci previously proposed in rodents. We discuss possible reasons for this difference based on the transposable element insertion histories in the rodent and primate lineages.
引用
收藏
页数:6
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