Literature DB >> 19186248

Fraying at the edge mouse models of diseases resulting from defects at the nuclear periphery.

Tatiana V Cohen1, Colin L Stewart.   

Abstract

Eukaryotic cells compartmentalize their genetic material within the nucleus. The boundary separating the genetic material from the cytoplasm is the nuclear envelope (NE) and lamina. Historically, the NE was perceived as functioning primarily as a barrier regulating the entry and exit of macromolecules between the nucleus and cytoplasm via the nuclear pore complexes (NPCs) that traverse the nuclear membranes. However, recent findings have caused a fundamental reassessment with regard to NE and lamina functions. Evidence now points to the NE and lamina functioning as a "hub" in regulating and perhaps integrating critical cellular functions that include chromatin organization, transcriptional regulation, mechanical integrity of the cell, signaling pathways, as well as acting as a key component of the cytoskeleton. Such an integral role for the nuclear boundary has emerged from increased interest into the functions of the NE/lamina, which has been largely stimulated by the discovery that some 24 different diseases and anomalies are caused by defects in proteins of the NE and lamina.

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Year:  2008        PMID: 19186248     DOI: 10.1016/S0070-2153(08)00607-8

Source DB:  PubMed          Journal:  Curr Top Dev Biol        ISSN: 0070-2153            Impact factor:   4.897


  7 in total

1.  Generation and characterization of a conditional deletion allele for Lmna in mice.

Authors:  Youngjo Kim; Yixian Zheng
Journal:  Biochem Biophys Res Commun       Date:  2013-08-30       Impact factor: 3.575

2.  Mouse B-type lamins are required for proper organogenesis but not by embryonic stem cells.

Authors:  Youngjo Kim; Alexei A Sharov; Katie McDole; Melody Cheng; Haiping Hao; Chen-Ming Fan; Nicholas Gaiano; Minoru S H Ko; Yixian Zheng
Journal:  Science       Date:  2011-11-24       Impact factor: 47.728

Review 3.  Dynamic chromosome movements during meiosis: a way to eliminate unwanted connections?

Authors:  Romain Koszul; Nancy Kleckner
Journal:  Trends Cell Biol       Date:  2009-10-23       Impact factor: 20.808

Review 4.  Nuclear lamin functions and disease.

Authors:  Veronika Butin-Israeli; Stephen A Adam; Anne E Goldman; Robert D Goldman
Journal:  Trends Genet       Date:  2012-07-12       Impact factor: 11.639

5.  Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy.

Authors:  Viola F Gnocchi; Juergen Scharner; Zhe Huang; Ken Brady; Jaclyn S Lee; Robert B White; Jennifer E Morgan; Yin-Biao Sun; Juliet A Ellis; Peter S Zammit
Journal:  PLoS One       Date:  2011-02-22       Impact factor: 3.240

6.  Pairing of homologous chromosomes in C. elegans meiosis requires DEB-1 - an orthologue of mammalian vinculin.

Authors:  Jana Rohožková; Lenka Hůlková; Jana Fukalová; Petr Flachs; Pavel Hozák
Journal:  Nucleus       Date:  2019-12       Impact factor: 4.197

7.  Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.

Authors:  Tatiana V Cohen; Viola F Gnocchi; Jonathan E Cohen; Aditi Phadke; Henry Liu; Juliet A Ellis; Roland Foisner; Colin L Stewart; Peter S Zammit; Terence A Partridge
Journal:  Hum Mol Genet       Date:  2013-03-27       Impact factor: 6.150

  7 in total

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