Abundance of female-biased and paucity of male-biased somatically expressed genes on the mouse X-chromosome [Elektronisk resurs]
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- Reinius, Björn (författare)
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Alternativt namn: Reinius, Björn
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Johansson, Martin (författare)
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Radomska, Katarzyna (författare)
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Morrow, Edward H (författare)
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Pandey, Gaurav Kumar (författare)
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Chandrasekhar, Kanduri (författare)
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Sandberg, Rickard (författare)
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Williams, Robert W (författare)
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Jazin, Elena (författare)
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Uppsala universitet Teknisk-naturvetenskapliga vetenskapsområdet (utgivare)
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Uppsala universitet Medicinska och farmaceutiska vetenskapsområdet (utgivare)
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Jazin Elena (medarbetare)
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Jazin Elena (medarbetare)
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Jazin Elena (medarbetare)
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Jazin Elena (medarbetare)
- 2012
- Engelska.
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Ingår i: BMC Genomics. - 1471-2164. ; 13, 607
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Sammanfattning
Ämnesord
Stäng
- 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.
Ämnesord
- Natural Sciences (hsv)
- Biological Sciences (hsv)
- Genetics (hsv)
- Naturvetenskap (hsv)
- Biologiska vetenskaper (hsv)
- Genetik (hsv)
- Genetics (uu)
- Genetik (uu)
- Biologi med inriktning mot zoologisk utvecklingsbiologi (uu)
- Biology with specialization in Animal Development (uu)
- Biology with specialization in Molecular Biology (uu)
- Biologi med inriktning mot molekylärbiologi (uu)
Indexterm och SAB-rubrik
- X-chromosome
- Sex chromosome; Somatic; Gene expression; Sexual antagonism; Sexual selection; Gender; Sex-bias; Female-bias; Male-bias; Sexual dimorphism; Dosage compensation; X-inactivation; Escape; Feminisation; Masculinisation; De-masculinisation; Microarray; Non-coding RNA; lncRNA; Tmem29; Kdm5c; Xist
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