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PMID: 2225074 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

RAP1 protein interacts with yeast telomeres in vivo: overproduction alters telomere structure and decreases chromosome stability.

Cell ·Vol. 63 ·No. 4 ·1990-11-16 ·Pages 739-50

Conrad MN, Wright JH, Wolf AJ, Zakian VA

Abstract

The protein encoded by the RAP1 gene of S. cerevisiae binds in vitro to a consensus sequence occurring at a number of sites in the yeast genome, including the repeated sequence C2-3A(CA)1-6 found at yeast telomeres. We present two lines of evidence for the in vivo binding of RAP1 protein at telomeres: first, RAP1 is present in telomeric chromatin and second, alterations in the level of RAP1 protein affect telomere length. The length changes seen with under- and overexpression of RAP1 are consistent with the interpretation that RAP1 binding to telomeres protects them from degradation. Unexpectedly, overproduction of the RAP1 protein was also shown to decrease greatly chromosome stability, suggesting that RAP1 mediates interactions that have a more global effect on chromosome behavior than simply protecting telomeres from degradation. Such interactions may involve telomere associations both with other telomeres and/or with structural elements of the nucleus.

MeSH Terms
Base Sequence Chromatin/physiology,ultrastructure Chromosome Deletion Chromosomes, Fungal/physiology DNA, Fungal/genetics DNA-Binding Proteins/genetics Fungal Proteins/genetics,metabolism Genes, Fungal Molecular Sequence Data Plasmids Recombination, Genetic Restriction Mapping Saccharomyces cerevisiae/genetics,physiology Transcription Factors
Chemicals
Chromatin DNA, Fungal DNA-Binding Proteins Fungal Proteins Transcription Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Conrad M N
Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.
Wright J H
Wolf A J
Zakian V A
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1990-11-16
Pages
739-50
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM43265 · United States
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