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Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order

BACKGROUND: We generated the gene expression profile of the total testis from the adult C57BL/6J male mice using serial analysis of gene expression (SAGE). Two high-quality SAGE libraries containing a total of 76 854 tags were constructed. An extensive bioinformatic analysis and comparison of SAGE t...

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Autores principales: Divina, Petr, Vlček, Čestmír, Strnad, Petr, Pačes, Václav, Forejt, Jiří
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1079818/
https://www.ncbi.nlm.nih.gov/pubmed/15748293
http://dx.doi.org/10.1186/1471-2164-6-29
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author Divina, Petr
Vlček, Čestmír
Strnad, Petr
Pačes, Václav
Forejt, Jiří
author_facet Divina, Petr
Vlček, Čestmír
Strnad, Petr
Pačes, Václav
Forejt, Jiří
author_sort Divina, Petr
collection PubMed
description BACKGROUND: We generated the gene expression profile of the total testis from the adult C57BL/6J male mice using serial analysis of gene expression (SAGE). Two high-quality SAGE libraries containing a total of 76 854 tags were constructed. An extensive bioinformatic analysis and comparison of SAGE transcriptomes of the total testis, testicular somatic cells and other mouse tissues was performed and the theory of male-biased gene accumulation on the X chromosome was tested. RESULTS: We sorted out 829 genes predominantly expressed from the germinal part and 944 genes from the somatic part of the testis. The genes preferentially and specifically expressed in total testis and testicular somatic cells were identified by comparing the testis SAGE transcriptomes to the available transcriptomes of seven non-testis tissues. We uncovered chromosomal clusters of adjacent genes with preferential expression in total testis and testicular somatic cells by a genome-wide search and found that the clusters encompassed a significantly higher number of genes than expected by chance. We observed a significant 3.2-fold enrichment of the proportion of X-linked genes specific for testicular somatic cells, while the proportions of X-linked genes specific for total testis and for other tissues were comparable. In contrast to the tissue-specific genes, an under-representation of X-linked genes in the total testis transcriptome but not in the transcriptomes of testicular somatic cells and other tissues was detected. CONCLUSION: Our results provide new evidence in favor of the theory of male-biased genes accumulation on the X chromosome in testicular somatic cells and indicate the opposite action of the meiotic X-inactivation in testicular germ cells.
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spelling pubmed-10798182005-04-15 Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order Divina, Petr Vlček, Čestmír Strnad, Petr Pačes, Václav Forejt, Jiří BMC Genomics Research Article BACKGROUND: We generated the gene expression profile of the total testis from the adult C57BL/6J male mice using serial analysis of gene expression (SAGE). Two high-quality SAGE libraries containing a total of 76 854 tags were constructed. An extensive bioinformatic analysis and comparison of SAGE transcriptomes of the total testis, testicular somatic cells and other mouse tissues was performed and the theory of male-biased gene accumulation on the X chromosome was tested. RESULTS: We sorted out 829 genes predominantly expressed from the germinal part and 944 genes from the somatic part of the testis. The genes preferentially and specifically expressed in total testis and testicular somatic cells were identified by comparing the testis SAGE transcriptomes to the available transcriptomes of seven non-testis tissues. We uncovered chromosomal clusters of adjacent genes with preferential expression in total testis and testicular somatic cells by a genome-wide search and found that the clusters encompassed a significantly higher number of genes than expected by chance. We observed a significant 3.2-fold enrichment of the proportion of X-linked genes specific for testicular somatic cells, while the proportions of X-linked genes specific for total testis and for other tissues were comparable. In contrast to the tissue-specific genes, an under-representation of X-linked genes in the total testis transcriptome but not in the transcriptomes of testicular somatic cells and other tissues was detected. CONCLUSION: Our results provide new evidence in favor of the theory of male-biased genes accumulation on the X chromosome in testicular somatic cells and indicate the opposite action of the meiotic X-inactivation in testicular germ cells. BioMed Central 2005-03-05 /pmc/articles/PMC1079818/ /pubmed/15748293 http://dx.doi.org/10.1186/1471-2164-6-29 Text en Copyright © 2005 Divina et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Divina, Petr
Vlček, Čestmír
Strnad, Petr
Pačes, Václav
Forejt, Jiří
Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order
title Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order
title_full Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order
title_fullStr Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order
title_full_unstemmed Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order
title_short Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order
title_sort global transcriptome analysis of the c57bl/6j mouse testis by sage: evidence for nonrandom gene order
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1079818/
https://www.ncbi.nlm.nih.gov/pubmed/15748293
http://dx.doi.org/10.1186/1471-2164-6-29
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