Nucleic Acids Research, Vol 26, Issue 18 4222-4229, Copyright © 1998 by Oxford University Press
CL Doe, G Wang, C Chow, MD Fricker, PB Singh and EJ Mellor
In eukaryotes, the segregation of chromosomes is co-ordinated by the
centromere and must proceed accurately if aneuploidy and cell death are to
be avoided. The fission yeast centromere is complex, containing highly
repetitive regions of DNA showing the characteristics of heterochromatin.
Two proteins, Swi6p and Clr4p, that are associated with the fission yeast
centromere also contain a chromo (chromatin organisation modifier) domain
and are required for centromere function. We have analysed a novel fission
yeast gene encoding a putative chromo domain called chp 1(+) (chromo domain
protein in Schizosaccharomyces p ombe ). In the absence of Chp1p protein,
cells are viable but show chromosome segregation defects such as lagging
chromosomes on the spindle during anaphase and high rates of minichromosome
loss, phenotypes which are also displayed by swi 6 and clr 4. A fusion
protein between green fluorescent protein (GFP) and Chp1p, like Swi6p, is
localized to discrete sites within the nucleus. In contrast to Swi6p and
Clr4p, Chp1p is not required to repress silent mating-type genes. We
demonstrate a genetic interaction between chp 1(+) and alpha-tubulin ( nda
2(+)) and between swi 6(+) and beta-tubulin ( nda 3(+)). Chp1p and Swi6p
proteins may be components of the kinetochore which captures and stabilizes
the microtubules of the spindle.
ARTICLES
The fission yeast chromo domain encoding gene chp1(+) is required for chromosome segregation and shows a genetic interaction with alpha- tubulin
Microbiology Unit, Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK, Department of Development and Genetics, The Babraham Institute, Babraham Hall, Babraham, Cambridge CB2 4AT, UK.
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