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Building up the nucleus: Nuclear organization in the establishment of totipotency and pluripotency during mammalian development.

Genes Dev. 30, 611-621 (2016)
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In mammals, epigenetic reprogramming, the acquisition and loss of totipotency, and the first cell fate decision all occur within a 3-d window after fertilization from the one-cell zygote to the formation of the blastocyst. These processes are poorly understood in molecular detail, yet this is an essential prerequisite to uncover principles of stem cells, chromatin biology, and thus regenerative medicine. A unique feature of preimplantation development is the drastic genome-wide changes occurring to nuclear architecture. From studying somatic and in vitro cultured embryonic stem cells (ESCs) it is becoming increasingly established that the three-dimensional (3D) positions of genomic loci relative to each other and to specific compartments of the nucleus can act on the regulation of gene expression, potentially driving cell fate. However, the functionality, mechanisms, and molecular characteristics of the changes in nuclear organization during preimplantation development are only now beginning to be unraveled. Here, we discuss the peculiarities of nuclear compartments and chromatin organization during mammalian preimplantation development in the context of the transition from totipotency to pluripotency.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Mouse Embryo ; Nuclear Architecture ; Totipotency; Embryonic Stem-cells; Lamin-b Receptor; A-type Lamin; Mouse Preimplantation Development; Order Chromatin Arrangements; In-situ Hybridization; De-novo Formation; Pore Complex; Domain Organization; Ribosomal Dna
Sprache
Veröffentlichungsjahr 2016
HGF-Berichtsjahr 2016
ISSN (print) / ISBN 0890-9369
e-ISSN 1549-5477
Zeitschrift Genes and Development
Quellenangaben Band: 30, Heft: 6, Seiten: 611-621 Artikelnummer: , Supplement: ,
Verlag Cold Spring Harbor Laboratory Press
Verlagsort Cold Spring Harbor
Begutachtungsstatus Peer reviewed
POF Topic(s) 30204 - Cell Programming and Repair
Forschungsfeld(er) Stem Cell and Neuroscience
PSP-Element(e) G-506200-001
Scopus ID 84961186840
PubMed ID 26980186
Erfassungsdatum 2016-03-23