Literature DB >> 27235113

Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans.

Marta Sanchez-Delgado1, Andrea Riccio2, Thomas Eggermann3, Eamonn R Maher4, Pablo Lapunzina5, Deborah Mackay6, David Monk7.   

Abstract

Eight syndromes are associated with the loss of methylation at specific imprinted loci. There has been increasing evidence that these methylation defects in patients are not isolated events occurring at a given disease-associated locus but that some of these patients may have multi-locus imprinting disturbances (MLID) affecting additional imprinted regions. With the recent advances in technology, methylation profiling has revealed that imprinted loci represent only a small fraction of the methylation differences observed between the gametes. To figure out how imprinting anomalies occur at multiple imprinted domains, we have to understand the interplay between DNA methylation and histone modifications in the process of selective imprint protection during pre-implantation reprogramming, which, if disrupted, leads to these complex imprinting disorders (IDs).
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  NLRPs; ZFP57; germline methylation; imprinting; multi-locus imprinting disturbances

Mesh:

Year:  2016        PMID: 27235113     DOI: 10.1016/j.tig.2016.05.001

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  31 in total

Review 1.  Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains.

Authors:  David Monk; Joannella Morales; Johan T den Dunnen; Silvia Russo; Franck Court; Dirk Prawitt; Thomas Eggermann; Jasmin Beygo; Karin Buiting; Zeynep Tümer
Journal:  Epigenetics       Date:  2018-01-25       Impact factor: 4.528

2.  Transgenerational paternal transmission of acquired traits: Stress-induced modification of the sperm regulatory transcriptome and offspring phenotypes.

Authors:  Terence Y C Pang; Annabel K Short; Timothy W Bredy; Anthony J Hannan
Journal:  Curr Opin Behav Sci       Date:  2017-03-08

Review 3.  Role of DNA methylation in imprinting disorders: an updated review.

Authors:  Amr Rafat Elhamamsy
Journal:  J Assist Reprod Genet       Date:  2017-03-09       Impact factor: 3.412

4.  Screening for rare epigenetic variations in autism and schizophrenia.

Authors:  Paras Garg; Andrew J Sharp
Journal:  Hum Mutat       Date:  2019-03-21       Impact factor: 4.878

5.  Ongoing Challenges in the Diagnosis of 11p15.5-Associated Imprinting Disorders.

Authors:  Deborah J G Mackay; I Karen Temple
Journal:  Mol Diagn Ther       Date:  2022-05-06       Impact factor: 4.074

Review 6.  Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics.

Authors:  M M A M Mannens; M P Lombardi; M Alders; P Henneman; J Bliek
Journal:  Front Genet       Date:  2022-07-04       Impact factor: 4.772

7.  Mendelian and non-Mendelian genetics in model plants.

Authors:  Ortrun Mittelsten Scheid
Journal:  Plant Cell       Date:  2022-07-04       Impact factor: 12.085

Review 8.  Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.

Authors:  Frédéric Brioude; Jennifer M Kalish; Alessandro Mussa; Alison C Foster; Jet Bliek; Giovanni Battista Ferrero; Susanne E Boonen; Trevor Cole; Robert Baker; Monica Bertoletti; Guido Cocchi; Carole Coze; Maurizio De Pellegrin; Khalid Hussain; Abdulla Ibrahim; Mark D Kilby; Malgorzata Krajewska-Walasek; Christian P Kratz; Edmund J Ladusans; Pablo Lapunzina; Yves Le Bouc; Saskia M Maas; Fiona Macdonald; Katrin Õunap; Licia Peruzzi; Sylvie Rossignol; Silvia Russo; Caroleen Shipster; Agata Skórka; Katrina Tatton-Brown; Jair Tenorio; Chiara Tortora; Karen Grønskov; Irène Netchine; Raoul C Hennekam; Dirk Prawitt; Zeynep Tümer; Thomas Eggermann; Deborah J G Mackay; Andrea Riccio; Eamonn R Maher
Journal:  Nat Rev Endocrinol       Date:  2018-01-29       Impact factor: 43.330

9.  Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure.

Authors:  Thomas Eggermann
Journal:  Geburtshilfe Frauenheilkd       Date:  2021-07-13       Impact factor: 2.915

10.  Maternal 5mCpG Imprints at the PARD6G-AS1 and GCSAML Differentially Methylated Regions Are Decoupled From Parent-of-Origin Expression Effects in Multiple Human Tissues.

Authors:  Graziela de Sá Machado Araújo; Ronaldo da Silva Francisco Junior; Cristina Dos Santos Ferreira; Pedro Thyago Mozer Rodrigues; Douglas Terra Machado; Thais Louvain de Souza; Jozimara Teixeira de Souza; Cleiton Figueiredo Osorio da Silva; Antônio Francisco Alves da Silva; Claudia Caixeta Franco Andrade; Alan Tardin da Silva; Victor Ramos; Ana Beatriz Garcia; Filipe Brum Machado; Enrique Medina-Acosta
Journal:  Front Genet       Date:  2018-03-01       Impact factor: 4.599

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