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Abundance of female-biased and paucity of male-biased somatically expressed genes on the mouse X-chromosome.

Authors :
Reinius, Bj�rn
Johansson, Martin M.
Radomska, Katarzyna J.
Morrow, Edward H.
Pandey, Gaurav K.
Kanduri, Chandrasekhar
Sandberg, Rickard
Williams, Robert W.
Jazin, Elena
Source :
BMC Genomics. 2012, Vol. 13 Issue 1, p607-624. 18p. 1 Color Photograph, 2 Charts, 5 Graphs.
Publication Year :
2012

Abstract

Background: Empirical evaluations of sexually dimorphic expression of genes on the mammalian X-chromosome are needed to understand the evolutionary forces and the gene-regulatory mechanisms controlling this chromosome. We performed a large-scale sex-bias expression analysis of genes on the X-chromosome in six different somatic tissues from mouse. Results: Our results show that the mouse X-chromosome is enriched with female-biased genes and depleted of male-biased genes. This suggests that feminisation as well as de-masculinisation of the X-chromosome has occurred in terms of gene expression in non-reproductive tissues. Several mechanisms may be responsible for the control of female-biased expression on chromosome X, and escape from X-inactivation is a main candidate. We confirmed escape in case of Tmem29 using RNA-FISH analysis. In addition, we identified novel female-biased non-coding transcripts located in the same female-biased cluster as the well-known coding X-inactivation escapee Kdm5c, likely transcribed from the transition-region between active and silenced domains. We also found that previously known escapees only partially explained the overrepresentation of female-biased X-genes, particularly for tissue-specific female-biased genes. Therefore, the gene set we have identified contains tissue-specific escapees and/or genes controlled by other sexually skewed regulatory mechanisms. Analysis of gene age showed that evolutionarily old X-genes (>100 myr, preceding the radiation of placental mammals) are more frequently female-biased than younger genes. Conclusion: Altogether, our results have implications for understanding both gene regulation and gene evolution of mammalian X-chromosomes, and suggest that the final result in terms of the X-gene composition (masculinisation versus feminisation) is a compromise between different evolutionary forces acting on reproductive and somatic tissues. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712164
Volume :
13
Issue :
1
Database :
Academic Search Index
Journal :
BMC Genomics
Publication Type :
Academic Journal
Accession number :
85711297
Full Text :
https://doi.org/10.1186/1471-2164-13-607