| Title: | The Rho-GEF Rom2p localizes to sites of polarized cell growth and participates in cytoskeletal functions in Saccharomyces cerevisiae |
| Author(s): | Manning BD; Padmanabha R; Snyder M; |
| Address: | "Department of Biology, Yale University, New Haven, Connecticut 06520-8103, USA" |
| ISSN/ISBN: | 1059-1524 (Print) 1059-1524 (Linking) |
| Abstract: | "Rom2p is a GDP/GTP exchange factor for Rho1p and Rho2p GTPases; Rho proteins have been implicated in control of actin cytoskeletal rearrangements. ROM2 and RHO2 were identified in a screen for high-copy number suppressors of cik1 delta, a mutant defective in microtubule-based processes in Saccharomyces cerevisiae. A Rom2p::3XHA fusion protein localizes to sites of polarized cell growth, including incipient bud sites, tips of small buds, and tips of mating projections. Disruption of ROM2 results in temperature-sensitive growth defects at 11 degrees C and 37 degrees C. rom2 delta cells exhibit morphological defects. At permissive temperatures, rom2 delta cells often form elongated buds and fail to form normal mating projections after exposure to pheromone; at the restrictive temperature, small budded cells accumulate. High-copy number plasmids containing either ROM2 or RHO2 suppress the temperature-sensitive growth defects of cik1 delta and kar3 delta strains. KAR3 encodes a kinesin-related protein that interacts with Cik1p. Furthermore, rom2 delta strains exhibit increased sensitivity to the microtubule depolymerizing drug benomyl. These results suggest a role for Rom2p in both polarized morphogenesis and functions of the microtubule cytoskeleton" |
| Keywords: | Binding Sites Cell Division/*physiology Cell Polarity Cytoskeleton/*physiology GTP-Binding Proteins/*analysis/*physiology Microtubules/metabolism Pheromones/pharmacology Saccharomyces cerevisiae/*chemistry/*physiology Saccharomyces cerevisiae Proteins *rh; |
| Notes: | "MedlineManning, B D Padmanabha, R Snyder, M eng GM36494/GM/NIGMS NIH HHS/ GM52197/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. 1997/12/31 Mol Biol Cell. 1997 Oct; 8(10):1829-44. doi: 10.1091/mbc.8.10.1829" |
