Literature DB >> 15657620

Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes.

Osman El-Maarri1, Muhieddine Seoud, Jean-Baptiste Rivière, Johannes Oldenburg, Jörn Walter, Guy Rouleau, Rima Slim.   

Abstract

In molar tissues from patients with recurrent biparental hydatidiform moles, we could previously demonstrate that differentially methylated regions (DMRs) of four imprinted genes are abnormally methylated on the maternal alleles. It remained unclear if this abnormal methylation originated de novo in the molar tissues or if it is even recognizable in the patient somatic tissues. To address this question, we investigated the DNA methylation of four imprinted genes in total blood from the two sister-patients. Here, we show that both patients retain normal methylation levels at the DMRs of the four genes in blood tissues. For two maternally expressed genes, we could use informative SNPs to follow the inheritance of the abnormally methylated maternal alleles in the molar tissues. We find that the transmitted abnormally methylated maternal alleles to the moles originated from the maternal grandmother and that the same alleles are not methylated in the patients. Our data suggest that the abnormal methylation in familial biparental molar tissues was acquired de novo in the patients'germline as a result of a false reprogramming or during the postzygotic development of the conceptuses that led to moles.

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Year:  2005        PMID: 15657620     DOI: 10.1038/sj.ejhg.5201353

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  4 in total

1.  Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation.

Authors:  Ugljesa Djuric; Osman El-Maarri; Barbara Lamb; Rork Kuick; Muheiddine Seoud; Philippe Coullin; Johannes Oldenburg; Samir Hanash; Rima Slim
Journal:  Hum Genet       Date:  2006-07-28       Impact factor: 4.132

2.  NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation.

Authors:  Sangeetha Mahadevan; Shu Wen; Ying-Wooi Wan; Hsiu-Huei Peng; Subhendu Otta; Zhandong Liu; Michelina Iacovino; Elisabeth M Mahen; Michael Kyba; Bekim Sadikovic; Ignatia B Van den Veyver
Journal:  Hum Mol Genet       Date:  2013-09-18       Impact factor: 6.150

3.  Diagnostic reproducibility of hydatidiform moles: ancillary techniques (p57 immunohistochemistry and molecular genotyping) improve morphologic diagnosis.

Authors:  Russell Vang; Mamta Gupta; Lee-Shu-Fune Wu; Anna V Yemelyanova; Robert J Kurman; Kathleen M Murphy; Cheryl Descipio; Brigitte M Ronnett
Journal:  Am J Surg Pathol       Date:  2012-03       Impact factor: 6.394

4.  The Diagnosis of Choriocarcinoma in Molar Pregnancies: A Revised Approach in Clinical Testing.

Authors:  Lisa Duffy; Liangtao Zhang; Karen Sheath; Donald R Love; Alice M George
Journal:  J Clin Med Res       Date:  2015-10-23
  4 in total

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