Literature DB >> 22964839

Structure and function in the budding yeast nucleus.

Angela Taddei1, Susan M Gasser.   

Abstract

Budding yeast, like other eukaryotes, carries its genetic information on chromosomes that are sequestered from other cellular constituents by a double membrane, which forms the nucleus. An elaborate molecular machinery forms large pores that span the double membrane and regulate the traffic of macromolecules into and out of the nucleus. In multicellular eukaryotes, an intermediate filament meshwork formed of lamin proteins bridges from pore to pore and helps the nucleus reform after mitosis. Yeast, however, lacks lamins, and the nuclear envelope is not disrupted during yeast mitosis. The mitotic spindle nucleates from the nucleoplasmic face of the spindle pole body, which is embedded in the nuclear envelope. Surprisingly, the kinetochores remain attached to short microtubules throughout interphase, influencing the position of centromeres in the interphase nucleus, and telomeres are found clustered in foci at the nuclear periphery. In addition to this chromosomal organization, the yeast nucleus is functionally compartmentalized to allow efficient gene expression, repression, RNA processing, genomic replication, and repair. The formation of functional subcompartments is achieved in the nucleus without intranuclear membranes and depends instead on sequence elements, protein-protein interactions, specific anchorage sites at the nuclear envelope or at pores, and long-range contacts between specific chromosomal loci, such as telomeres. Here we review the spatial organization of the budding yeast nucleus, the proteins involved in forming nuclear subcompartments, and evidence suggesting that the spatial organization of the nucleus is important for nuclear function.

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Year:  2012        PMID: 22964839      PMCID: PMC3430528          DOI: 10.1534/genetics.112.140608

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  227 in total

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2.  The Slx5-Slx8 complex affects sumoylation of DNA repair proteins and negatively regulates recombination.

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3.  Silent information regulator 2 family of NAD- dependent histone/protein deacetylases generates a unique product, 1-O-acetyl-ADP-ribose.

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4.  DNA polymerases alpha, delta, and epsilon localize and function together at replication forks in Saccharomyces cerevisiae.

Authors:  Shin-Ichiro Hiraga; Aki Hagihara-Hayashi; Tomoko Ohya; Akio Sugino
Journal:  Genes Cells       Date:  2005-04       Impact factor: 1.891

5.  Localization of Sir2p: the nucleolus as a compartment for silent information regulators.

Authors:  M Gotta; S Strahl-Bolsinger; H Renauld; T Laroche; B K Kennedy; M Grunstein; S M Gasser
Journal:  EMBO J       Date:  1997-06-02       Impact factor: 11.598

6.  SUMOylation regulates telomere length homeostasis by targeting Cdc13.

Authors:  Lisa E Hang; Xianpeng Liu; Iris Cheung; Yan Yang; Xiaolan Zhao
Journal:  Nat Struct Mol Biol       Date:  2011-07-10       Impact factor: 15.369

7.  Physical mapping of the MEL gene family in Saccharomyces cerevisiae.

Authors:  H Turakainen; G Naumov; E Naumova; M Korhola
Journal:  Curr Genet       Date:  1993-12       Impact factor: 3.886

8.  Silent domains are assembled continuously from the telomere and are defined by promoter distance and strength, and by SIR3 dosage.

Authors:  H Renauld; O M Aparicio; P D Zierath; B L Billington; S K Chhablani; D E Gottschling
Journal:  Genes Dev       Date:  1993-07       Impact factor: 11.361

9.  DNA sequences of telomeres maintained in yeast.

Authors:  J Shampay; J W Szostak; E H Blackburn
Journal:  Nature       Date:  1984 Jul 12-18       Impact factor: 49.962

10.  Mutually exclusive binding of telomerase RNA and DNA by Ku alters telomerase recruitment model.

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  82 in total

1.  Conserved forkhead dimerization motif controls DNA replication timing and spatial organization of chromosomes in S. cerevisiae.

Authors:  A Zachary Ostrow; Reza Kalhor; Yan Gan; Sandra K Villwock; Christian Linke; Matteo Barberis; Lin Chen; Oscar M Aparicio
Journal:  Proc Natl Acad Sci U S A       Date:  2017-03-06       Impact factor: 11.205

Review 2.  Something silent this way forms: the functional organization of the repressive nuclear compartment.

Authors:  Joan C Ritland Politz; David Scalzo; Mark Groudine
Journal:  Annu Rev Cell Dev Biol       Date:  2013-07-05       Impact factor: 13.827

Review 3.  The multifunctional nuclear pore complex: a platform for controlling gene expression.

Authors:  Christopher Ptak; John D Aitchison; Richard W Wozniak
Journal:  Curr Opin Cell Biol       Date:  2014-03-22       Impact factor: 8.382

4.  General method for rapid purification of native chromatin fragments.

Authors:  Vyacheslav I Kuznetsov; Spencer A Haws; Catherine A Fox; John M Denu
Journal:  J Biol Chem       Date:  2018-05-24       Impact factor: 5.157

Review 5.  Exploring the three-dimensional organization of genomes: interpreting chromatin interaction data.

Authors:  Job Dekker; Marc A Marti-Renom; Leonid A Mirny
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Review 6.  Protein lysine acetylation by p300/CBP.

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7.  Perinuclear tethers license telomeric DSBs for a broad kinesin- and NPC-dependent DNA repair process.

Authors:  Daniel K C Chung; Janet N Y Chan; Jonathan Strecker; Wei Zhang; Sasha Ebrahimi-Ardebili; Thomas Lu; Karan J Abraham; Daniel Durocher; Karim Mekhail
Journal:  Nat Commun       Date:  2015-07-24       Impact factor: 14.919

8.  A SIR-independent role for cohesin in subtelomeric silencing and organization.

Authors:  Deepash Kothiwal; Shikha Laloraya
Journal:  Proc Natl Acad Sci U S A       Date:  2019-03-06       Impact factor: 11.205

Review 9.  The challenge of staying in shape: nuclear size matters.

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Journal:  Curr Genet       Date:  2021-03-29       Impact factor: 3.886

Review 10.  Budding yeast for budding geneticists: a primer on the Saccharomyces cerevisiae model system.

Authors:  Andrea A Duina; Mary E Miller; Jill B Keeney
Journal:  Genetics       Date:  2014-05       Impact factor: 4.562

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