JCB logo
Quantitative Colocalization Analysis Software
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow Full Text
Right arrow Full Text (PDF, 582K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Freeman, L.
Right arrow Articles by Strunnikov, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Freeman, L.
Right arrow Articles by Strunnikov, A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

© The Rockefeller University Press, 0021-9525/2000//811 $5.00
The Journal of Cell Biology, Volume 149, Number 4, , 2000 811-824


Original Article

The Condensin Complex Governs Chromosome Condensation and Mitotic Transmission of Rdna



Lita Freemana, Luis Aragon-Alcaidea, and Alexander Strunnikova

a Unit of Chromosome Structure and Function, National Institutes of Health, National Institute of Child Health and Human Development, Laboratory of Molecular Embryology, Bethesda, Maryland 20892-5430
Laboratory of Molecular Embryology, National Institutes of Health, National Institute of Child Health and Human Development, Unit of Chromosome Structure and Function, 18T Library Drive, Room 106, Bethesda, MD 20892-5340.(301) 402-1323(301) 402-1323

strunnik{at}box-s.nih.gov

We have characterized five genes encoding condensin components in Saccharomyces cerevisiae. All genes are essential for cell viability and encode proteins that form a complex in vivo. We characterized new mutant alleles of the genes encoding the core subunits of this complex, smc2-8 and smc4-1. Both SMC2 and SMC4 are essential for chromosome transmission in anaphase. Mutations in these genes cause defects in establishing condensation of unique (chromosome VIII arm) and repetitive (rDNA) regions of the genome but do not impair sister chromatid cohesion. In vivo localization of Smc4p fused to green fluorescent protein showed that, unexpectedly, in S. cerevisiae the condensin complex concentrates in the rDNA region at the G2/M phase of the cell cycle. rDNA segregation in mitosis is delayed and/or stalled in smc2 and smc4 mutants, compared with separation of pericentromeric and distal arm regions. Mitotic transmission of chromosome III carrying the rDNA translocation is impaired in smc2 and smc4 mutants. Thus, the condensin complex in S. cerevisiae has a specialized function in mitotic segregation of the rDNA locus. Chromatin immunoprecipitation (ChIP) analysis revealed that condensin is physically associated with rDNA in vivo. Thus, the rDNA array is the first identified set of DNA sequences specifically bound by condensin in vivo. The biological role of higher-order chromosome structure in S. cerevisiae is discussed.

Key Words: SMC • condensin • chromosome condensation • chromosome segregation • chromatin



© 2000 The Rockefeller University Press

Abbreviations used in this paper: ARS, DNA replication origin; ChIP, chromatin immunoprecipitation; FISH, fluorescent in situ hybridization; GFP, green fluorescent protein; HA, hemagglutinin; YAC, yeast artificial chromosome.



Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?




  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents