Ekwall K, Nimmo E R, Javerzat J P, Borgstrøm B, Egel R, Cranston G, Allshire R
MRC Human Genetics Unit, Western General Hospital, Edinburgh, Scotland, UK.
J Cell Sci. 1996 Nov;109 ( Pt 11):2637-48. doi: 10.1242/jcs.109.11.2637.
Transcriptional silencing is known to occur at centromeres, telomeres and the mating type region in the nucleus of fission yeast, Schizosaccharomyces pombe. Mating-type silencing factors have previously been shown also to affect transcriptional repression within centromeres and to some extent at telomeres. Mutations in the clr4+, rik1+ and swi6+ genes dramatically reduce silencing at certain centromeric regions and cause elevated chromosome loss rates. Recently, Swi6p was found to co-localise with the three silent chromosomal regions. Here the involvement of clr4+, rik1+ and swi6+ in centromere function is investigated in further detail. Fluorescence in situ hybridisation (FISH) was used to show that, as in swi6 mutant cells, centromeres lag on late anaphase spindles in clr4 and rik1 mutant cells. This phenotype is consistent with a role for these three gene products in fission yeast centromere function. The Swi6 protein was found to be delocalised from all three silent chromosomal regions, and dispersed within the nucleus, in both clr4 and rik1 mutant cells. The phenotypic similarity observed in all three mutants is consistent with the products of both the clr4+ and rik1+ genes being required to recruit Swi6p to the centromere and other silent regions. Mutations in clr4, rik1 and swi6 also result in elevated sensitivity to reagents which destabilise microtubules and show a synergistic interaction with a mutation in the beta-tubulin gene (nda3). These observations suggest that clr4+ and rik1+ must play a role in the assembly of Swi6p into a transcriptionally silent, inaccessible chromatin structure at fission yeast centromeres which is required to facilitate interactions with spindle microtubules and to ensure normal chromosome segregation.
已知转录沉默发生在裂殖酵母粟酒裂殖酵母细胞核中的着丝粒、端粒和交配型区域。先前已表明,交配型沉默因子也会影响着丝粒内以及在一定程度上端粒处的转录抑制。clr4 +、rik1 +和swi6 +基因的突变会显著降低某些着丝粒区域的沉默,并导致染色体丢失率升高。最近,发现Swi6p与三个沉默染色体区域共定位。在此,对clr4 +、rik1 +和swi6 +在着丝粒功能中的作用进行了更详细的研究。荧光原位杂交(FISH)用于表明,与swi6突变细胞一样,clr4和rik1突变细胞中的着丝粒在后期纺锤体上滞后。这种表型与这三种基因产物在裂殖酵母着丝粒功能中的作用一致。在clr4和rik1突变细胞中,发现Swi6蛋白从所有三个沉默染色体区域中脱离,并分散在细胞核内。在所有三个突变体中观察到表型相似性,这与clr4 +和rik1 +基因的产物都需要将Swi6p募集到着丝粒和其他沉默区域一致。clr4、rik1和swi6中的突变还导致对破坏微管的试剂敏感性增加,并与β -微管蛋白基因(nda3)中的突变表现出协同相互作用。这些观察结果表明,clr4 +和rik1 +必须在将Swi6p组装成裂殖酵母着丝粒处转录沉默、无法接近且便于与纺锤体微管相互作用并确保正常染色体分离所需的染色质结构中发挥作用。