A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients
<p>Abstract</p> <p>Background</p> <p>The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is present in at least 1 out of 4,500 female live births and is the second most common cause for primary amenorrhea. It is characterized by vaginal and uterine aplasia in an XX indiv...
| Main Authors: | , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2011-05-01
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| Series: | Orphanet Journal of Rare Diseases |
| Online Access: | http://www.ojrd.com/content/6/1/32 |
| _version_ | 1819045009451646976 |
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| author | Riess Olaf Schoenfisch Birgitt Schaeferhoff Karin Haebig Karina Poths Sven Walter Michael Barresi Gianmaria Rall Katharina Wallwiener Diethelm Bonin Michael Brucker Sara |
| author_facet | Riess Olaf Schoenfisch Birgitt Schaeferhoff Karin Haebig Karina Poths Sven Walter Michael Barresi Gianmaria Rall Katharina Wallwiener Diethelm Bonin Michael Brucker Sara |
| author_sort | Riess Olaf |
| collection | DOAJ |
| description | <p>Abstract</p> <p>Background</p> <p>The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is present in at least 1 out of 4,500 female live births and is the second most common cause for primary amenorrhea. It is characterized by vaginal and uterine aplasia in an XX individual with normal secondary characteristics. It has long been considered a sporadic anomaly, but familial clustering occurs. Several candidate genes have been studied although no single factor has yet been identified. Cases of discordant monozygotic twins suggest that the involvement of epigenetic factors is more likely.</p> <p>Methods</p> <p>Differences in gene expression and methylation patterns of uterine tissue between eight MRKH patients and eight controls were identified using whole-genome microarray analyses. Results obtained by expression and methylation arrays were confirmed by qRT-PCR and pyrosequencing.</p> <p>Results</p> <p>We delineated 293 differentially expressed and 194 differentially methylated genes of which nine overlap in both groups. These nine genes are mainly embryologically relevant for the development of the female genital tract.</p> <p>Conclusion</p> <p>Our study used, for the first time, a combined whole-genome expression and methylation approach to reveal the etiology of the MRKH syndrome. The findings suggest that either deficient estrogen receptors or the ectopic expression of certain <it>HOXA </it>genes might lead to abnormal development of the female reproductive tract. <it>In utero </it>exposure to endocrine disruptors or abnormally high maternal hormone levels might cause ectopic expression or anterior transformation of <it>HOXA </it>genes. It is, however, also possible that different factors influence the anti-Mullerian hormone promoter activity during embryological development causing regression of the Müllerian ducts. Thus, our data stimulate new research directions to decipher the pathogenic basis of MRKH syndrome.</p> |
| first_indexed | 2024-12-21T10:21:45Z |
| format | Article |
| id | doaj.art-d0deffcf829f41f396dcdfdf1cb21f9c |
| institution | Directory Open Access Journal |
| issn | 1750-1172 |
| language | English |
| last_indexed | 2024-12-21T10:21:45Z |
| publishDate | 2011-05-01 |
| publisher | BMC |
| record_format | Article |
| series | Orphanet Journal of Rare Diseases |
| spelling | doaj.art-d0deffcf829f41f396dcdfdf1cb21f9c2022-12-21T19:07:25ZengBMCOrphanet Journal of Rare Diseases1750-11722011-05-01613210.1186/1750-1172-6-32A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patientsRiess OlafSchoenfisch BirgittSchaeferhoff KarinHaebig KarinaPoths SvenWalter MichaelBarresi GianmariaRall KatharinaWallwiener DiethelmBonin MichaelBrucker Sara<p>Abstract</p> <p>Background</p> <p>The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is present in at least 1 out of 4,500 female live births and is the second most common cause for primary amenorrhea. It is characterized by vaginal and uterine aplasia in an XX individual with normal secondary characteristics. It has long been considered a sporadic anomaly, but familial clustering occurs. Several candidate genes have been studied although no single factor has yet been identified. Cases of discordant monozygotic twins suggest that the involvement of epigenetic factors is more likely.</p> <p>Methods</p> <p>Differences in gene expression and methylation patterns of uterine tissue between eight MRKH patients and eight controls were identified using whole-genome microarray analyses. Results obtained by expression and methylation arrays were confirmed by qRT-PCR and pyrosequencing.</p> <p>Results</p> <p>We delineated 293 differentially expressed and 194 differentially methylated genes of which nine overlap in both groups. These nine genes are mainly embryologically relevant for the development of the female genital tract.</p> <p>Conclusion</p> <p>Our study used, for the first time, a combined whole-genome expression and methylation approach to reveal the etiology of the MRKH syndrome. The findings suggest that either deficient estrogen receptors or the ectopic expression of certain <it>HOXA </it>genes might lead to abnormal development of the female reproductive tract. <it>In utero </it>exposure to endocrine disruptors or abnormally high maternal hormone levels might cause ectopic expression or anterior transformation of <it>HOXA </it>genes. It is, however, also possible that different factors influence the anti-Mullerian hormone promoter activity during embryological development causing regression of the Müllerian ducts. Thus, our data stimulate new research directions to decipher the pathogenic basis of MRKH syndrome.</p>http://www.ojrd.com/content/6/1/32 |
| spellingShingle | Riess Olaf Schoenfisch Birgitt Schaeferhoff Karin Haebig Karina Poths Sven Walter Michael Barresi Gianmaria Rall Katharina Wallwiener Diethelm Bonin Michael Brucker Sara A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients Orphanet Journal of Rare Diseases |
| title | A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients |
| title_full | A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients |
| title_fullStr | A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients |
| title_full_unstemmed | A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients |
| title_short | A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients |
| title_sort | combination of transcriptome and methylation analyses reveals embryologically relevant candidate genes in mrkh patients |
| url | http://www.ojrd.com/content/6/1/32 |
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