Literature DB >> 19879952

Genomic imprinting effects in a compromised in utero environment: implications for a healthy pregnancy.

A L Lim1, A C Ferguson-Smith.   

Abstract

Genomic imprinting in gametogenesis marks a subset of mammalian genes for parent-of-origin-dependent monoallelic expression in the offspring. In mice, the identification and manipulation of individual imprinted genes has shown that the diverse products of these genes are largely devoted to controlling pre- and postnatal growth. Human syndromes with parental origin effects have been characterized both at the phenotypic and genotypic levels, allowing further elucidation of the function and regulation of imprinted genes. Evidence suggests that a compromised in utero environment influences fetal growth through the modulation of epigenetic states. However it is not known whether imprinted genes, by their nature, might be more or less susceptible to such environmental influences. Here we review the progress made in addressing the influence of a compromised in utero environment on the behavior of imprinted genes. We also examine whether these environmental influences may have an impact on the later development of human disease. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19879952     DOI: 10.1016/j.semcdb.2009.10.008

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  18 in total

1.  Effects of endocrine disruptors on imprinted gene expression in the mouse embryo.

Authors:  Eun-Rim Kang; Khursheed Iqbal; Diana A Tran; Guillermo E Rivas; Purnima Singh; Gerd P Pfeifer; Piroska E Szabó
Journal:  Epigenetics       Date:  2011-07-01       Impact factor: 4.528

2.  Reproductive issues in anorexia nervosa.

Authors:  Elizabeth R Hoffman; Stephanie C Zerwas; Cynthia M Bulik
Journal:  Expert Rev Obstet Gynecol       Date:  2011-07

3.  Superovulation alters the expression of endometrial genes critical to tissue remodeling and placentation.

Authors:  Suneeta Senapati; Fan Wang; Teri Ord; Christos Coutifaris; Rui Feng; Monica Mainigi
Journal:  J Assist Reprod Genet       Date:  2018-06-29       Impact factor: 3.412

4.  Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques.

Authors:  Cristina Camprubí; Marta Pladevall; Mark Grossmann; Nicolás Garrido; Maria Carme Pons; Joan Blanco
Journal:  Epigenetics       Date:  2012-08-13       Impact factor: 4.528

5.  Methylation loss at H19 imprinted gene correlates with methylenetetrahydrofolate reductase gene promoter hypermethylation in semen samples from infertile males.

Authors:  John C Rotondo; Rita Selvatici; Maura Di Domenico; Roberto Marci; Fortunato Vesce; Mauro Tognon; Fernanda Martini
Journal:  Epigenetics       Date:  2013-07-24       Impact factor: 4.528

Review 6.  Brain function and chromatin plasticity.

Authors:  Catherine Dulac
Journal:  Nature       Date:  2010-06-10       Impact factor: 49.962

7.  Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic systems in mouse placenta.

Authors:  Anne Gabory; Laure Ferry; Isabelle Fajardy; Luc Jouneau; Jean-David Gothié; Alexandre Vigé; Cécile Fleur; Sylvain Mayeur; Catherine Gallou-Kabani; Marie-Sylvie Gross; Linda Attig; Anne Vambergue; Jean Lesage; Brigitte Reusens; Didier Vieau; Claude Remacle; Jean-Philippe Jais; Claudine Junien
Journal:  PLoS One       Date:  2012-11-05       Impact factor: 3.240

8.  DNA methylation patterns in cord blood DNA and body size in childhood.

Authors:  Caroline L Relton; Alexandra Groom; Beate St Pourcain; Adrian E Sayers; Daniel C Swan; Nicholas D Embleton; Mark S Pearce; Susan M Ring; Kate Northstone; Jon H Tobias; Joseph Trakalo; Andy R Ness; Seif O Shaheen; George Davey Smith
Journal:  PLoS One       Date:  2012-03-14       Impact factor: 3.240

9.  No Evidence for a Parent-of-Origin Specific Differentially Methylated Region Linked to RASGRF1.

Authors:  Punita Navnitlal Pitamber; Zané Lombard; Michèle Ramsay
Journal:  Front Genet       Date:  2012-03-28       Impact factor: 4.599

10.  Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.

Authors:  Anne Rieusset; Fabienne Schaller; Unga Unmehopa; Valery Matarazzo; Françoise Watrin; Matthias Linke; Beatrice Georges; Jocelyn Bischof; Femke Dijkstra; Monique Bloemsma; Severine Corby; François J Michel; Rachel Wevrick; Ulrich Zechner; Dick Swaab; Keith Dudley; Laurent Bezin; Françoise Muscatelli
Journal:  PLoS Genet       Date:  2013-09-05       Impact factor: 5.917

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