Genetic characterisation of hda1+, a putative fission yeast histone deacetylase gene

被引:26
作者
Olsson, TGS
Ekwall, K
Allshire, RC
Sunnerhagen, P
Partridge, JF
Richardson, WA
机构
[1] Univ Goteborg, Lundberg Lab, Dept Mol Biol, S-40530 Gothenburg, Sweden
[2] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
基金
英国惠康基金;
关键词
D O I
10.1093/nar/26.13.3247
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
hda1(+) (histone deacetylase 1) is a fission yeast gene which is highly similar in sequence to known histone deacetylase genes in humans and budding yeast. We have investigated if this putative histone deacetylase contributes to transcriptional silencing in the fission yeast Schizosaccharomyces pombe. A precise deletion allele of the hda1(+) open reading frame was created. Cells lacking the hda1(+) gene are viable. However, genetic analysis reveals that cells without hda1(+) display enhanced gene repression/silencing of marker genes, residing adjacent to telomeres, close to the silent mating-type loci and within centromere I. This phenotype is very similar to that recently reported for rpd3 mutants both in Drosophila and budding yeast. No defects in chromosome segregation or changes in telomere length were detected. Cells lacking the hda1(+) gene display reduced sporulation. Growth of hda1 cells is partially inhibited by low concentrations of Trichostatin A (TSA), a known inhibitor of histone deacetylase enzymes. TSA treatment is also able to overcome the enhanced silencing found in heterochromatic regions of hda1 cells. These results indicate a genetic redundancy with respect to deacetylase genes and partially overlapping functions of these in fission yeast. The significance of these results is discussed in the light of recent discoveries from other eukaryotes.
引用
收藏
页码:3247 / 3254
页数:8
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