Origin and evolution of a placental-specific microRNA family in the human genome

<p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are a class of short regulatory RNAs encoded in the genome of DNA viruses, some single cell organisms, plants and animals. With the rapid development of technology, more and more miRNAs are being discovered. Howeve...

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Main Authors: Gong Lejun, Lu Zhiyuan, Ding Yan, Jiang Dongke, Sun Xiao, Yuan Zhidong, Liu Hongde, Xie Jianming
Format: Article
Language:English
Published: BMC 2010-11-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/10/346
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author Gong Lejun
Lu Zhiyuan
Ding Yan
Jiang Dongke
Sun Xiao
Yuan Zhidong
Liu Hongde
Xie Jianming
author_facet Gong Lejun
Lu Zhiyuan
Ding Yan
Jiang Dongke
Sun Xiao
Yuan Zhidong
Liu Hongde
Xie Jianming
author_sort Gong Lejun
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are a class of short regulatory RNAs encoded in the genome of DNA viruses, some single cell organisms, plants and animals. With the rapid development of technology, more and more miRNAs are being discovered. However, the origin and evolution of most miRNAs remain obscure. Here we report the origin and evolution dynamics of a human miRNA family.</p> <p>Results</p> <p>We have shown that all members of the miR-1302 family are derived from MER53 elements. Although the conservation scores of the MER53-derived pre-miRNA sequences are low, we have identified 36 potential paralogs of MER53-derived miR-1302 genes in the human genome and 58 potential orthologs of the human miR-1302 family in placental mammals. We suggest that in placental species, this miRNA family has evolved following the birth-and-death model of evolution. Three possible mechanisms that can mediate miRNA duplication in evolutionary history have been proposed: the transposition of the MER53 element, segmental duplications and Alu-mediated recombination. Finally, we have found that the target genes of miR-1302 are over-represented in transportation, localization, and system development processes and in the positive regulation of cellular processes. Many of them are predicted to function in binding and transcription regulation.</p> <p>Conclusions</p> <p>The members of miR-1302 family that are derived from MER53 elements are placental-specific miRNAs. They emerged at the early stage of the recent 180 million years since eutherian mammals diverged from marsupials. Under the birth-and-death model, the miR-1302 genes have experienced a complex expansion with some members evolving by segmental duplications and some by Alu-mediated recombination events.</p>
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spelling doaj.art-65808a62dc424b8498813daa2dec7c3e2022-12-21T21:05:05ZengBMCBMC Evolutionary Biology1471-21482010-11-0110134610.1186/1471-2148-10-346Origin and evolution of a placental-specific microRNA family in the human genomeGong LejunLu ZhiyuanDing YanJiang DongkeSun XiaoYuan ZhidongLiu HongdeXie Jianming<p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are a class of short regulatory RNAs encoded in the genome of DNA viruses, some single cell organisms, plants and animals. With the rapid development of technology, more and more miRNAs are being discovered. However, the origin and evolution of most miRNAs remain obscure. Here we report the origin and evolution dynamics of a human miRNA family.</p> <p>Results</p> <p>We have shown that all members of the miR-1302 family are derived from MER53 elements. Although the conservation scores of the MER53-derived pre-miRNA sequences are low, we have identified 36 potential paralogs of MER53-derived miR-1302 genes in the human genome and 58 potential orthologs of the human miR-1302 family in placental mammals. We suggest that in placental species, this miRNA family has evolved following the birth-and-death model of evolution. Three possible mechanisms that can mediate miRNA duplication in evolutionary history have been proposed: the transposition of the MER53 element, segmental duplications and Alu-mediated recombination. Finally, we have found that the target genes of miR-1302 are over-represented in transportation, localization, and system development processes and in the positive regulation of cellular processes. Many of them are predicted to function in binding and transcription regulation.</p> <p>Conclusions</p> <p>The members of miR-1302 family that are derived from MER53 elements are placental-specific miRNAs. They emerged at the early stage of the recent 180 million years since eutherian mammals diverged from marsupials. Under the birth-and-death model, the miR-1302 genes have experienced a complex expansion with some members evolving by segmental duplications and some by Alu-mediated recombination events.</p>http://www.biomedcentral.com/1471-2148/10/346
spellingShingle Gong Lejun
Lu Zhiyuan
Ding Yan
Jiang Dongke
Sun Xiao
Yuan Zhidong
Liu Hongde
Xie Jianming
Origin and evolution of a placental-specific microRNA family in the human genome
BMC Evolutionary Biology
title Origin and evolution of a placental-specific microRNA family in the human genome
title_full Origin and evolution of a placental-specific microRNA family in the human genome
title_fullStr Origin and evolution of a placental-specific microRNA family in the human genome
title_full_unstemmed Origin and evolution of a placental-specific microRNA family in the human genome
title_short Origin and evolution of a placental-specific microRNA family in the human genome
title_sort origin and evolution of a placental specific microrna family in the human genome
url http://www.biomedcentral.com/1471-2148/10/346
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