Genomic Imprinting and Physiological Processes in Mammals.


Journal

Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066

Informations de publication

Date de publication:
21 02 2019
Historique:
received: 26 06 2018
revised: 08 01 2019
accepted: 24 01 2019
entrez: 23 2 2019
pubmed: 23 2 2019
medline: 7 1 2020
Statut: ppublish

Résumé

Complex multicellular organisms, such as mammals, express two complete sets of chromosomes per nucleus, combining the genetic material of both parents. However, epigenetic studies have demonstrated violations to this rule that are necessary for mammalian physiology; the most notable parental allele expression phenomenon is genomic imprinting. With the identification of endogenous imprinted genes, genomic imprinting became well-established as an epigenetic mechanism in which the expression pattern of a parental allele influences phenotypic expression. The expanding study of genomic imprinting is revealing a significant impact on brain functions and associated diseases. Here, we review key milestones in the field of imprinting and discuss mechanisms and systems in which imprinted genes exert a significant role.

Identifiants

pubmed: 30794780
pii: S0092-8674(19)30106-0
doi: 10.1016/j.cell.2019.01.043
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

952-965

Subventions

Organisme : Wellcome Trust
ID : 210757/Z/18/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 210757/Z/18
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L010305/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/K011332/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/P002307/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S000437/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/B/000C0426
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R009791/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/P008623/1
Pays : United Kingdom

Investigateurs

Valter Tucci (V)
Marisa S Bartolomei (MS)
Nissim Benvenisty (N)
Déborah Bourc'his (D)
Marika Charalambous (M)
Catherine Dulac (C)
Robert Feil (R)
Juliane Glaser (J)
Lisa Huelsmann (L)
Rosalind M John (RM)
Gráinne I McNamara (GI)
Kim Moorwood (K)
Francoise Muscatelli (F)
Hiroyuki Sasaki (H)
Beverly I Strassmann (BI)
Claudius Vincenz (C)
Jon Wilkins (J)
Anthony R Isles (AR)
Gavin Kelsey (G)
Anne C Ferguson-Smith (AC)

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Valter Tucci (V)

Department of Neuroscience and Brain Technologies - Istituto Italiano di Tecnologia, via Morego, 30, 16163, Genova, Italy. Electronic address: valter.tucci@iit.it.

Anthony R Isles (AR)

MRC Centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Cardiff University, Cardiff, CF24 44H, UK.

Gavin Kelsey (G)

Epigenetics Programme, Babraham Institute, Cambridge, CB22 3AT, UK; Centre for Trophoblast Research, University of Cambridge, Cambridge, CB2 3EG, UK.

Anne C Ferguson-Smith (AC)

Department of Genetics, University of Cambridge, Downing Street, Cambridge CB2 3EH, UK.

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Classifications MeSH