Modulation of Cell Identity by Modification of Nuclear Pore Complexes

被引:8
作者
Gomar-Alba, Merce [1 ,2 ,3 ,4 ]
Mendoza, Manuel [1 ,2 ,3 ,4 ]
机构
[1] Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France
[2] CNRS, Illkirch Graffenstaden, France
[3] Inst Natl Sante & Rech Med, Illkirch Graffenstaden, France
[4] Univ Strasbourg, Strasbourg, France
关键词
nuclear pore complex; cell differentiation; deacetylase; budding yeast; Hos3; TRANSCRIPTIONAL MEMORY; GENE; NUCLEOPORIN; EXPRESSION; LOCALIZATION; RECRUITMENT; RNA; REORGANIZATION; ARCHITECTURE; MAINTENANCE;
D O I
10.3389/fgene.2019.01301
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Nuclear pore complexes (NPCs) are protein assemblies that form channels across the nuclear envelope to mediate communication between the nucleus and the cytoplasm. Additionally, NPCs interact with chromatin and influence the position and expression of multiple genes. Interestingly, the composition of NPCs can vary in different cell-types, tissues, and developmental states. Here, we review recent findings suggesting that modifications of NPC composition, including post-translational modifications, play an instructive role in cell fate establishment. In particular, we focus on the role of cell-specific NPC deacetylation in asymmetrically dividing budding yeast, which modulates transport-dependent and transport-independent NPC functions to determine the time of commitment to a new division cycle in daughter cells. By modulating protein localization and gene expression, NPCs are therefore emerging as central regulators of cell identity.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] The Nuclear Pore Complex as a Transcription Regulator
    Summer, Michael Chas
    Brickner, Jason
    COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2022, 14 (01):
  • [32] The C-terminal domain of Nup93 is essential for assembly of the structural backbone of nuclear pore complexes
    Sachdev, Ruchika
    Sieverding, Cornelia
    Floetenmeyer, Matthias
    Antonin, Wolfram
    MOLECULAR BIOLOGY OF THE CELL, 2012, 23 (04) : 740 - 749
  • [33] Nuclear envelope insertion of spindle pole bodies and nuclear pore complexes
    Jaspersen, Sue L.
    Ghosh, Suman
    NUCLEUS, 2012, 3 (03) : 226 - 236
  • [34] Nuclear size, nuclear pore number and cell cycle
    Maeshima, Kazuhiro
    Iino, Haruki
    Hihara, Saera
    Imamoto, Naoko
    NUCLEUS, 2011, 2 (02) : 113 - 118
  • [35] Analysis of the Lotus japonicus nuclear pore NUP107-160 subcomplex reveals pronounced structural plasticity and functional redundancy
    Binder, Andreas
    Parniske, Martin
    FRONTIERS IN PLANT SCIENCE, 2014, 4
  • [36] A Change in Nuclear Pore Complex Composition Regulates Cell Differentiation
    D'Angelo, Maximilian A.
    Gomez-Cavazos, J. Sebastian
    Mei, Arianna
    Lackner, Daniel H.
    Hetzer, Martin W.
    DEVELOPMENTAL CELL, 2012, 22 (02) : 446 - 458
  • [37] Kinetic analysis of translocation through nuclear pore complexes
    Ribbeck, K
    Görlich, D
    EMBO JOURNAL, 2001, 20 (06) : 1320 - 1330
  • [38] Characterisation of the passive permeability barrier of nuclear pore complexes
    Mohr, Dagmar
    Frey, Steffen
    Fischer, Torsten
    Guettler, Thomas
    Goerlich, Dirk
    EMBO JOURNAL, 2009, 28 (17) : 2541 - 2553
  • [39] Advances in the understanding of nuclear pore complexes in human diseases
    Li, Yuxuan
    Zhu, Jie
    Zhai, Fengguang
    Kong, Lili
    Li, Hong
    Jin, Xiaofeng
    JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2024, 150 (07)
  • [40] Nuclear Pore Complexes: A Scaffold Regulating Developmental Transcription?
    Satomura, Atsushi
    Brickner, Jason H.
    TRENDS IN CELL BIOLOGY, 2017, 27 (09) : 621 - 622