Afshar K, Scholey J, Hawley R S
Section of Molecular and Cellular Biology, University of California at Davis 95616, USA.
J Cell Biol. 1995 Nov;131(4):833-43. doi: 10.1083/jcb.131.4.833.
The nod kinesin-like protein is localized along the arms of meiotic chromosomes and is required to maintain the position of achiasmate chromosomes on the developing meiotic spindle. Here we show that the localization of ectopically expressed nod protein on mitotic chromosomes precisely parallels that observed for wild-type nod protein on meiotic chromosomes. Moreover, the carboxyl-terminal half of the nod protein also binds to chromosomes when overexpressed in mitotic cells, whereas the overexpressed amino-terminal motor domain binds only to microtubules. Chromosome localization of the carboxyl-terminal domain of nod depends upon an 82-amino acid region comprised of three copies of a sequence homologous to the DNA-binding domain of HMG 14/17 proteins. These data map the two primary functional domains of the nod protein in vivo and provide a molecular explanation for the directing of the nod protein to a specific subcellular component, the chromosome.
结节样驱动蛋白定位于减数分裂染色体的臂上,对于维持无交叉染色体在发育中的减数分裂纺锤体上的位置是必需的。我们在此表明,异位表达的结节蛋白在有丝分裂染色体上的定位与野生型结节蛋白在减数分裂染色体上的定位精确平行。此外,当在有丝分裂细胞中过表达时,结节蛋白的羧基末端一半也与染色体结合,而过表达的氨基末端运动结构域仅与微管结合。结节蛋白羧基末端结构域的染色体定位取决于一个由82个氨基酸组成的区域,该区域由与HMG 14/17蛋白的DNA结合结构域同源的序列的三个拷贝组成。这些数据在体内定位了结节蛋白的两个主要功能结构域,并为将结节蛋白导向特定亚细胞成分——染色体提供了分子解释。