| Title : Ric-8A and Gi alpha recruit LGN, NuMA, and dynein to the cell cortex to help orient the mitotic spindle - Woodard_2010_Mol.Cell.Biol_30_3519 |
| Author(s) : Woodard GE , Huang NN , Cho H , Miki T , Tall GG , Kehrl JH |
| Ref : Molecular & Cellular Biology , 30 :3519 , 2010 |
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Abstract :
In model organisms, resistance to inhibitors of cholinesterase 8 (Ric-8), a G protein alpha (G alpha) subunit guanine nucleotide exchange factor (GEF), functions to orient mitotic spindles during asymmetric cell divisions; however, whether Ric-8A has any role in mammalian cell division is unknown. We show here that Ric-8A and G alpha(i) function to orient the metaphase mitotic spindle of mammalian adherent cells. During mitosis, Ric-8A localized at the cell cortex, spindle poles, centromeres, central spindle, and midbody. Pertussis toxin proved to be a useful tool in these studies since it blocked the binding of Ric-8A to G alpha(i), thus preventing its GEF activity for G alpha(i). Linking Ric-8A signaling to mammalian cell division, treatment of cells with pertussis toxin, reduction of Ric-8A expression, or decreased G alpha(i) expression similarly affected metaphase cells. Each treatment impaired the localization of LGN (GSPM2), NuMA (microtubule binding nuclear mitotic apparatus protein), and dynein at the metaphase cell cortex and disturbed integrin-dependent mitotic spindle orientation. Live cell imaging of HeLa cells expressing green fluorescent protein-tubulin also revealed that reduced Ric-8A expression prolonged mitosis, caused occasional mitotic arrest, and decreased mitotic spindle movements. These data indicate that Ric-8A signaling leads to assembly of a cortical signaling complex that functions to orient the mitotic spindle. |
| PubMedSearch : Woodard_2010_Mol.Cell.Biol_30_3519 |
| PubMedID: 20479129 |
Woodard GE, Huang NN, Cho H, Miki T, Tall GG, Kehrl JH (2010)
Ric-8A and Gi alpha recruit LGN, NuMA, and dynein to the cell cortex to help orient the mitotic spindle
Molecular & Cellular Biology
30 :3519
Woodard GE, Huang NN, Cho H, Miki T, Tall GG, Kehrl JH (2010)
Molecular & Cellular Biology
30 :3519