Ypt11 functions in bud-directed transport of the Golgi by linking Myo2 to the coatomer subunit Ret2

被引:47
作者
Arai, Seisuke [1 ]
Noda, Yoichi [1 ]
Kainuma, Satoko [1 ]
Wada, Ikuo [2 ,3 ]
Yoda, Koji [1 ]
机构
[1] Univ Tokyo, Dept Biotechnol, Bunkyo Ku, Tokyo 1138657, Japan
[2] Fukushima Med Univ, Sch Med, Inst Biomed Sci, Dept Cell Sci, Fukushima 9601295, Japan
[3] JST, CREST, Saitama 3320012, Japan
基金
日本学术振兴会;
关键词
D O I
10.1016/j.cub.2008.06.028
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 yeast class V myosin Myo2 transports the Golgi into the bud during its inheritance [1]. However, the mechanism that links the Golgi to Myo2 is unknown. Here, we report that Ypt11, a Rab GTPase that reportedly interacts with Myo2, binds to Ret2, a subunit of the coatomer complex. When Ypt11 is overproduced, Ret2 and the Golgi markers, Och1 and Sft2, are accumulated in the growing bud and are lost in the mother cell. In a ret2 mutant that produces the Ret2 protein with reduced affinity to Ypt11, no such accumulation is observed upon overproduction of Ypt11. At a certain stage of budding, it is known that the late Golgi cisternae labeled with Sec7-GFP show polarized distribution in the bud [1]. We find that this polarization of late Golgi cisternae is not observed in the ypt11 Delta mutant. Indeed, analyses of Sec7-GFP dynamics with spatio-temporal image correlation spectroscopy (STICS) and fluorescence loss in photo-bleaching (FLIP) reveals that Ypt11 is required for the vectorial actin-dependent movement of the late Golgi from the mother cell toward the emerging bud. These results indicate that the Ypt11 and Ret2 are components of a Myo2 receptor complex that functions during the Golgi inheritance into the growing bud.
引用
收藏
页码:987 / 991
页数:5
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