MCB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ercan, S.
Right arrow Articles by Simpson, R. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ercan, S.
Right arrow Articles by Simpson, R. T.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, November 2004, p. 10026-10035, Vol. 24, No. 22
0270-7306/04/$08.00+0     DOI: 10.1128/MCB.24.22.10026-10035.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Global Chromatin Structure of 45,000 Base Pairs of Chromosome III in a- and {alpha}-Cell Yeast and during Mating-Type Switching

Sevinc Ercan* and Robert T. Simpson{dagger}

Center for Gene Regulation and Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania

Received 28 June 2004/ Returned for modification 19 July 2004/ Accepted 24 August 2004

Directionality of yeast mating-type switching has been attributed to differences in chromatin structure for the left arm of chromosome III. We have mapped the structure of ~45 kbp of the left arm of chromosome III in a and {alpha} cells in logarithmically growing cultures and in a cells during switching. Distinctive features of chromatin structure were the occurrence of DNase I-hypersensitive sites in the promoter region of nearly every gene and some replication origins and the presence of extended regions of positioned nucleosomes in ~25% of the open reading frames. Other than the recombination enhancer, chromatin structures were identical in the two cell types. Changes in chromatin structure during switching were confined to the recombination enhancer. This unbiased analysis of an extended region of chromatin reveals that significant features of organized chromatin exist for the entire region, and these features are largely static with respect to mating type and mating-type switching. Our analysis also shows that primary chromatin structure does not cause the documented differences in recombinational frequency of the left arm of chromosome III in yeast a and {alpha} cells.


* Corresponding author. Mailing address: c/o Joseph Reese, 203 Althouse Laboratory, Penn State University, University Park, PA 16802. Phone: (814) 865-1976. Fax: (814) 863-7024. E-mail: jcr8{at}psu.edu.

{dagger} Deceased.


Molecular and Cellular Biology, November 2004, p. 10026-10035, Vol. 24, No. 22
0022-538X/04/$08.00+0     DOI: 10.1128/MCB.24.22.10026-10035.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2004 by the American Society for Microbiology. All rights reserved.