Miller Mark S, Esparza Jessica M, Lippa Andrew M, Lux Fordyce G, Cole Douglas G, Dutcher Susan K
Department of Microbiology, Molecular Biology, and Biochemistry, University of Idaho, Moscow, ID 83844-3052, USA.
Mol Biol Cell. 2005 Aug;16(8):3810-20. doi: 10.1091/mbc.e05-05-0404. Epub 2005 Jun 8.
The Chlamydomonas anterograde intraflagellar transport motor, kinesin-2, is isolated as a heterotrimeric complex containing two motor subunits and a nonmotor subunit known as kinesin-associated polypeptide or KAP. One of the two motor subunits is encoded by the FLA10 gene. The sequence of the second motor subunit was obtained by mass spectrometry and sequencing. It shows 46.9% identity with the Fla10 motor subunit and the gene maps to linkage group XII/XIII near RPL9. The temperature-sensitive flagellar assembly mutants fla1 and fla8 are linked to this kinesin-2 motor subunit. In each strain, a unique single point mutation gives rise to a unique single amino acid substitution within the motor domain. The fla8 strain is named fla8-1 and the fla1 strain is named fla8-2. The fla8 and fla10 alleles show a chromosome loss phenotype. To analyze this chromosome loss phenotype, intragenic revertants of fla8-1, fla8-2, and fla10-14 were generated. The analysis of the mutants and the revertants demonstrates the importance of a pocket in the amino terminus of these motor subunits for both motor activity and for a novel, dominant effect on the fidelity of chromosome segregation.
衣藻顺行鞭毛内运输马达蛋白驱动蛋白-2,被分离为一种异源三聚体复合物,包含两个马达亚基和一个非马达亚基,即驱动蛋白相关多肽或KAP。两个马达亚基之一由FLA10基因编码。通过质谱分析和测序获得了第二个马达亚基的序列。它与Fla10马达亚基的序列一致性为46.9%,该基因定位于靠近RPL9的连锁群XII/XIII。温度敏感型鞭毛组装突变体fla1和fla8与这种驱动蛋白-2马达亚基相关。在每个菌株中,一个独特的单点突变在马达结构域内产生一个独特的单氨基酸取代。fla8菌株命名为fla8-1,fla1菌株命名为fla8-2。fla8和fla10等位基因表现出染色体丢失表型。为了分析这种染色体丢失表型,产生了fla8-1、fla8-2和fla10-14的基因内回复突变体。对突变体和回复突变体的分析表明,这些马达亚基氨基末端的一个口袋对于马达活性以及对染色体分离保真度的一种新的显性效应都很重要。