Nuclear envelope-vacuole contacts mitigate nuclear pore complex assembly stress

被引:14
作者
Lord, Christopher L. [1 ]
Wente, Susan R. [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Cell & Dev Biol, Nashville, TN 37212 USA
基金
美国国家卫生研究院;
关键词
OXYSTEROL-BINDING PROTEIN; SACCHAROMYCES-CEREVISIAE; PIECEMEAL MICROAUTOPHAGY; MEMBRANE-PROTEINS; YEAST; NUCLEOPORINS; REQUIRES; EXPORT; IDENTIFICATION; LOCALIZATION;
D O I
10.1083/jcb.202001165
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The intricacy of nuclear pore complex (NPC) biogenesis imposes risks of failure that can cause defects in nuclear transport and nuclear envelope (NE) morphology; however, cellular mechanisms used to alleviate NPC assembly stress are not well defined. In the budding yeast Saccharomyces cerevisiae, we demonstrate that NVJ1- and MDM1-enriched NE-vacuole contacts increase when NPC assembly is compromised in several nup mutants, including nup116 Delta GLFG cells. These interorganelle nucleus-vacuole junctions (NVJs) cooperate with lipid droplets to maintain viability and enhance NPC formation in assembly mutants. Additionally, NVJs function with ATG1 to remodel the NE and promote vacuole-dependent degradation of specific nucleoporins in nup116 Delta GLFG cells. Importantly, NVJs significantly improve the physiology of NPC assembly mutants, despite having only negligible effects when NPC biogenesis is unperturbed. These results therefore define how NE-vacuole interorganelle contacts coordinate responses to mitigate deleterious cellular effects caused by disrupted NPC assembly.
引用
收藏
页数:24
相关论文
共 82 条
[1]   Nup120p: A yeast nucleoporin required for NPC distribution and mRNA transport [J].
Aitchison, JD ;
Blobel, G ;
Rout, MP .
JOURNAL OF CELL BIOLOGY, 1995, 131 (06) :1659-1675
[2]   The SND proteins constitute an alternative targeting route to the endoplasmic reticulum [J].
Aviram, Naama ;
Ast, Tslil ;
Costa, Elizabeth A. ;
Arakel, Eric C. ;
Chuartzman, Silvia G. ;
Jan, Calvin H. ;
Hassenteufel, Sarah ;
Dudek, Johanna ;
Jung, Martin ;
Schorr, Stefan ;
Zimmermann, Richard ;
Schwappach, Blanche ;
Weissman, Jonathan S. ;
Schuldiner, Maya .
NATURE, 2016, 540 (7631) :134-+
[3]   Competitive organelle-specific adaptors recruit Vps13 to membrane contact sites [J].
Bean, Bjorn D. M. ;
Dziurdzik, Samantha K. ;
Kolehmainen, Kathleen L. ;
Fowler, Claire M. S. ;
Kwong, Waldan K. ;
Grad, Leslie I. ;
Davey, Michael ;
Schluter, Cayetana ;
Conibear, Elizabeth .
JOURNAL OF CELL BIOLOGY, 2018, 217 (10) :3593-3607
[4]   The nuclear pore complex: understanding its function through structural insight [J].
Beck, Martin ;
Hurt, Ed .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (02) :73-89
[5]   Depletion of a single nucleoporin, Nup107, prevents the assembly of a subset of nucleoporins into the nuclear pore complex [J].
Boehmer, T ;
Enninga, J ;
Dales, S ;
Blobel, G ;
Zhong, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :981-985
[6]  
Brachmann CB, 1998, YEAST, V14, P115
[7]   A novel fluorescence-based genetic strategy identifies mutants of Saccharomyces cerevisiae defective for nuclear pore complex assembly [J].
Bucci, M ;
Wente, SR .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (09) :2439-2461
[8]   Nuclear pore complex integrity requires Lnp1, a regulator of cortical endoplasmic reticulum [J].
Casey, Amanda K. ;
Chen, Shuliang ;
Novick, Peter ;
Ferro-Novick, Susan ;
Wente, Susan R. .
MOLECULAR BIOLOGY OF THE CELL, 2015, 26 (15) :2833-2844
[9]   Pom33, a novel transmembrane nucleoporin required for proper nuclear pore complex distribution [J].
Chadrin, Anne ;
Hess, Barbara ;
San Roman, Mabel ;
Gatti, Xavier ;
Lombard, Berangere ;
Loew, Damarys ;
Barral, Yves ;
Palancade, Benoit ;
Doye, Valerie .
JOURNAL OF CELL BIOLOGY, 2010, 189 (05) :795-811
[10]   Age-Dependent Deterioration of Nuclear Pore Complexes Causes a Loss of Nuclear Integrity in Postmitotic Cells [J].
D'Angelo, Maximiliano A. ;
Raices, Marcela ;
Panowski, Siler H. ;
Hetzer, Martin W. .
CELL, 2009, 136 (02) :284-295