Abstract |
Abnormal centrosomal structures similar to those occurring in human cancers are induced in fission yeast by overexpression of the pericentrin homolog Pcp1p. Analysis of abnormal Pcp1p-containing structures with quantitative mass spectrometry and isotope-coded affinity tags identified a coiled-coil, structural maintenance of chromosomes (SMC) domain protein. This protein, termed Ccq1p (coiled-coil protein quantitatively enriched), localizes with Taz1p to telomeres in normal vegetative cells. Fluorescence resonance energy transfer (FRET) measurements indicate that Ccq1p also interacts with centrosomal Pcp1p in mating pheromone-stimulated cells containing centrosomally clustered telomeres. We provide evidence that the Ccq1p-Pcp1p interaction, while essential for meiosis, is deleterious when forced to occur during vegetative growth. Cells lacking one ccq1 allele exhibit a loss-of-function phenotype including abnormally long cell length, chromosome segregation failure, telomeric shortening, and defective telomeric clustering during meiotic prophase. Our data indicate a mechanism underlying meiotic chromosomal bouquet formation and suggest a recruitment model for supernumerary centrosome toxicity.
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Authors | Mark R Flory, Andrew R Carson, Eric G Muller, Ruedi Aebersold |
Journal | Molecular cell
(Mol Cell)
Vol. 16
Issue 4
Pg. 619-30
(Nov 19 2004)
ISSN: 1097-2765 [Print] United States |
PMID | 15546621
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- RNA, Messenger
- Schizosaccharomyces pombe Proteins
- Telomere-Binding Proteins
- taz1 protein, S pombe
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Topics |
- Alleles
- Cell Nucleus
(metabolism)
- Centrosome
(metabolism)
- Chromosomes, Fungal
- Fluorescence Resonance Energy Transfer
- Mass Spectrometry
- Meiosis
- Microscopy, Fluorescence
- Models, Biological
- Models, Molecular
- Oligonucleotide Array Sequence Analysis
- Open Reading Frames
- Peptide Mapping
- Plasmids
- Protein Structure, Tertiary
- RNA, Messenger
(metabolism)
- Schizosaccharomyces
(cytology, genetics, metabolism)
- Schizosaccharomyces pombe Proteins
(chemistry, genetics, metabolism)
- Telomere
(metabolism)
- Telomere-Binding Proteins
(metabolism)
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