Farkasovsky M, Küntzel H
Max-Planck-Institut für experimentelle Medizin, Göttingen, Federal Republic of Germany.
J Cell Biol. 1995 Nov;131(4):1003-14. doi: 10.1083/jcb.131.4.1003.
The NUM1 gene is involved in the control of nuclear migration in Saccharomyces cerevisiae. The content of NUM1 mRNA fluctuates during the cell cycle, reaching a maximum at S/G2 phase, and the translation product Num1p associates with the cortex of mother cells mainly during S, G2, and mitosis, as seen by indirect immunofluorescence. The nuclear spindle in NUM1-deficient large-budded cells often fails to align along the mother/bud axis, while abnormally elongated astral microtubules emanate from both spindle pole bodies. A num1 null mutation confers temperature sensitivity to the cold-sensitive alpha-tubulin mutant tub1-1, and shows synthetic lethality with the beta-tubulin mutant alleles tub2-402, tub2-403, tub2-404, and tub2-405. Deletion mapping has defined three functionally important Num1p regions: a potential EF hand Ca2+ binding site, a cluster of potential phosphorylation sites and a pleckstrin homology domain. The latter domain appears to be involved in targeting Num1p to the mother cell cortex. Our data suggest that the periodically expressed NUM1 gene product controls nuclear migration by affecting astral microtubule functions.
NUM1基因参与酿酒酵母中核迁移的调控。NUM1 mRNA的含量在细胞周期中波动,在S/G2期达到最大值,通过间接免疫荧光观察,翻译产物Num1p主要在S期、G2期和有丝分裂期间与母细胞的皮质相关联。NUM1缺陷的大芽细胞中的核纺锤体常常无法沿母细胞/芽轴排列,而异常伸长的星体微管从两个纺锤极体发出。num1缺失突变赋予对冷敏感的α-微管蛋白突变体tub1-1温度敏感性,并与β-微管蛋白突变等位基因tub2-402、tub2-403、tub2-404和tub2-405表现出合成致死性。缺失图谱确定了三个功能上重要的Num1p区域:一个潜在的EF手型Ca2+结合位点、一组潜在的磷酸化位点和一个普列克底物蛋白同源结构域。后一个结构域似乎参与将Num1p靶向到母细胞皮质。我们的数据表明,周期性表达的NUM1基因产物通过影响星体微管功能来控制核迁移。