spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online 15 May 2007
doi: 10.1242/jcs.03457


Journal of Cell Science 120, 1935-1943 (2007)
Published by The Company of Biologists 2007
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary Material
Right arrow All Versions of this Article:
jcs.03457v1
120/11/1935    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Alfredsson-Timmins, J.
Right arrow Articles by Bjerling, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Alfredsson-Timmins, J.
Right arrow Articles by Bjerling, P.

Research Article

The Clr4 methyltransferase determines the subnuclear localization of the mating-type region in fission yeast

Jenny Alfredsson-Timmins, Frida Henningson and Pernilla Bjerling*

University of Uppsala, Department of Medical Biochemistry and Microbiology (IMBIM), Box 582, SE-751 23 Uppsala, Sweden

* Author for correspondence (e-mail: Pernilla.Bjerling{at}imbim.uu.se)

Accepted 11 April 2007

The genome has a non-random spatial distribution in the cell nucleus. In Schizosaccharomyces pombe, it has been shown that the centromeres, telomeres and the mating-type region localize to the nuclear membrane (NM), the former by attaching to the spindle pole body (SPB). In addition, reporter genes inserted into these areas are transcriptionally repressed because of the formation of specialized chromatin structures. Performing live cell analysis we found that in a wild-type strain the mating-type region was positioned in the proximity of the SPB, the location where the pericentromeric heterochromatin is also found. In a strain lacking the histone methyltransferase Clr4, crucial for the formation of heterochromatin, the mating-type region had a random localization in the nucleus. Moreover, in a strain in which the two boundary elements IR-L and IR-R had been deleted, the mating-type region was displaced from its position at the proximity of the SPB, but remained in the vicinity of the NM. Moreover, in all investigated strains with silencing deficiencies the distance between the mating-type region and the SPB increased. This result indicates a correlation between transcriptional derepression and displacement of the region. Two different models of how the mating-type chromatin is organized in the nucleus are discussed.

Key words: Fission yeast, Heterochromatin, Silencing, Subnuclear localization




This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
M. Sadaie, R. Kawaguchi, Y. Ohtani, F. Arisaka, K. Tanaka, K. Shirahige, and J.-i. Nakayama
Balance between Distinct HP1 Family Proteins Controls Heterochromatin Assembly in Fission Yeast
Mol. Cell. Biol., December 1, 2008; 28(23): 6973 - 6988.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2007