Kinesin-dependent axonal transport is mediated by the Sunday driver (SYD) protein

被引:264
|
作者
Bowman, AB
Kamal, A
Ritchings, BW
Philp, AV
McGrail, M
Gindhart, JG
Goldstein, LSB
机构
[1] Univ Calif San Diego, Howard Hughes Med Inst, Dept Cellular & Mol Med, Dept Pharmacol, La Jolla, CA 92093 USA
[2] Univ Massachusetts, Dept Biol, Boston, MA 02125 USA
关键词
D O I
10.1016/S0092-8674(00)00162-8
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
A broadly conserved membrane-associated protein required for the functional interaction of kinesin-1 with axonal cargo was identified. Mutations in sunday driver (syd) and the axonal transport motor kinesin-1 cause similar phenotypes in Drosophila, including aberrant accumulations of axonal cargoes. GFP-tagged mammalian SYD localizes to tubulovesicular structures that costain for kinesin-1 and a marker of the secretory pathway. Coimmunoprecipitation analysis indicates that mouse SYD forms a complex with kinesin-1 in vivo. Yeast two-hybrid analysis and in vitro interaction studies reveal that SYD directly binds kinesin-1 via the tetratricopeptide repeat (TPR) domain of kinesin light chain (KLC) with K-d approximate to 200 nM. We propose that SYD mediates the axonal transport of at least one class of vesicles by interacting directly with KLC.
引用
收藏
页码:583 / 594
页数:12
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