Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?

<p>Abstract</p> <p>Background</p> <p>The Drosophila X-chromosome shows a significant underrepresentation of genes with male-biased gene expression (demasculinization). This trend is matched by retrogenes, which typically have a male biased gene expression pattern and sh...

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Main Authors: Metta Muralidhar, Schlötterer Christian
Format: Article
Language:English
Published: BMC 2010-04-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/10/114
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spelling doaj-9ab71cd243c24b52be1b1c6f3ba12b502021-09-02T04:35:10ZengBMCBMC Evolutionary Biology1471-21482010-04-0110111410.1186/1471-2148-10-114Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?Metta MuralidharSchlötterer Christian<p>Abstract</p> <p>Background</p> <p>The Drosophila X-chromosome shows a significant underrepresentation of genes with male-biased gene expression (demasculinization). This trend is matched by retrogenes, which typically have a male biased gene expression pattern and show a significant movement bias from X-chromosomes to autosomes. It is currently assumed that these patterns are best explained by selection, either mediated by male meiotic sex chromosome inactivation (MSCI) or sexually antagonistic forces. We scrutinized the evolutionary dynamics of retroposition by focusing on retrogenes for which the parental copy has degenerated.</p> <p>Results</p> <p>Consistent with a functional substitution of the degenerated gene by the retrogene, patterns of sequence evolution and gene expression were similar between retroposed and parental genes. Like previous studies, our set of retrogenes showed a significant movement off the X-chromosome. In contrast to data sets where retroposition caused gene duplication, the genes in our study showed primarily female-biased or unbiased gene expression.</p> <p>Conclusions</p> <p>Based on our results, the biased transposition pattern cannot be explained by MSCI and probably not by sexual antagonism. Rather, we propose that the movement away from the X-chromosome represents a general property of retroposition in Drosophila.</p> http://www.biomedcentral.com/1471-2148/10/114
collection DOAJ
language English
format Article
sources DOAJ
author Metta Muralidhar
Schlötterer Christian
spellingShingle Metta Muralidhar
Schlötterer Christian
Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?
BMC Evolutionary Biology
author_facet Metta Muralidhar
Schlötterer Christian
author_sort Metta Muralidhar
title Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?
title_short Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?
title_full Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?
title_fullStr Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?
title_full_unstemmed Non-random genomic integration - an intrinsic property of retrogenes in Drosophila?
title_sort non-random genomic integration - an intrinsic property of retrogenes in drosophila?
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2010-04-01
description <p>Abstract</p> <p>Background</p> <p>The Drosophila X-chromosome shows a significant underrepresentation of genes with male-biased gene expression (demasculinization). This trend is matched by retrogenes, which typically have a male biased gene expression pattern and show a significant movement bias from X-chromosomes to autosomes. It is currently assumed that these patterns are best explained by selection, either mediated by male meiotic sex chromosome inactivation (MSCI) or sexually antagonistic forces. We scrutinized the evolutionary dynamics of retroposition by focusing on retrogenes for which the parental copy has degenerated.</p> <p>Results</p> <p>Consistent with a functional substitution of the degenerated gene by the retrogene, patterns of sequence evolution and gene expression were similar between retroposed and parental genes. Like previous studies, our set of retrogenes showed a significant movement off the X-chromosome. In contrast to data sets where retroposition caused gene duplication, the genes in our study showed primarily female-biased or unbiased gene expression.</p> <p>Conclusions</p> <p>Based on our results, the biased transposition pattern cannot be explained by MSCI and probably not by sexual antagonism. Rather, we propose that the movement away from the X-chromosome represents a general property of retroposition in Drosophila.</p>
url http://www.biomedcentral.com/1471-2148/10/114
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