Ypt32p and Mlc1p bind within the vesicle binding region of the class V myosin Myo2p globular tail domain

被引:18
作者
Casavola, Elena Caroli [1 ,2 ]
Catucci, Alessandro [2 ]
Bielli, Pamela [1 ]
Di Pentima, Alessio [2 ]
Porcu, Giampiero [1 ,2 ]
Pennestri, Matteo [3 ]
Cicero, Daniel O. [3 ]
Ragnini-Wilson, Antonella [1 ,2 ]
机构
[1] Univ Roma Tor Vergata, Dept Biol, I-00173 Rome, Italy
[2] Consorzio Mario Negri Sud, Dept Cell Biol & Oncol, Santa Maria Imbaro, Italy
[3] Univ Roma Tor Vergata, Dept Chem Sci & Technol, NMR Lab, Rome, Italy
关键词
D O I
10.1111/j.1365-2958.2008.06106.x
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
Myosin V is an actin-based motor essential for a variety of cellular processes including skin pigmentation, cell separation and synaptic transmission. Myosin V transports organelles, vesicles and mRNA by binding, directly or indirectly, to cargo-bound receptors via its C-terminal globular tail domain (GTD). We have used the budding yeast myosin V Myo2p to shed light on the mechanism of how Myo2p interacts with post-Golgi carriers. We show that the Rab/Ypt protein Ypt32p, which associates with membranes of the trans-Golgi network, secretory vesicles and endosomes and is related to the mammalian Rab11, interacts with the Myo2p GTD within a region previously identified as the 'vesicle binding region'. Furthermore, we show that the essential myosin light chain 1 (Mlc1p), required for vesicle delivery at the mother-bud neck during cytokinesis, binds to the Myo2p GTD in a region overlapping that of Ypt32p. Our data are consistent with a role of Ypt32p and Mlc1p in regulating the interaction of post-Golgi carriers with Myo2p subdomain II.
引用
收藏
页码:1051 / 1066
页数:16
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