Lis1 is an initiation factor for dynein-driven organelle transport

被引:135
作者
Egan, Martin J. [1 ]
Tan, Kaeling [1 ]
Reck-Peterson, Samara L. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
MICROTUBULE PLUS-ENDS; EARLY-ENDOSOME INTERACTION; LISSENCEPHALY GENE LIS1; ASPERGILLUS-NIDULANS; CYTOPLASMIC DYNEIN; NEURONAL MIGRATION; NUCLEAR MIGRATION; AXONAL-TRANSPORT; BRAIN-DEVELOPMENT; BUDDING YEAST;
D O I
10.1083/jcb.201112101
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The molecular motor cytoplasmic dynein is responsible for most minus-end-directed, microtubule-based transport in eukaryotic cells. It is especially important in neurons, where defects in microtubule-based motility have been linked to neurological diseases. For example, lissencephaly is caused by mutations in the dynein-associated protein Lis1. In this paper, using the long, highly polarized hyphae of the filamentous fungus Aspergillus nidulans, we show that three morphologically and functionally distinct dynein cargos showed transport defects in the genetic absence of Lis1/nudF, raising the possibility that Lis1 is ubiquitously used for dynein-based transport. Surprisingly, both dynein and its cargo moved at normal speeds in the absence of Lis1 but with reduced frequency. Moreover, Lis1, unlike dynein and dynactin, was absent from moving dynein cargos, further suggesting that Lis1 is not required for dynein-based cargo motility once it has commenced. Based on these observations, we propose that Lis1 has a general role in initiating dynein-driven motility.
引用
收藏
页码:971 / 982
页数:12
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