Translational control as a novel regulator of gradient sensing and chemotropism in yeast
R. Gelin-Licht, P. J. Conlon, R. Singh, G. Haimovich, C. Baez, L. Gal, M. Schuldiner, A. Levchenko, J. E. Gerst
Abstract
The yeast mating pathway regulates haploid cell fusion in response to pheromone signaling via a mitogen-activated protein kinase (MAPK) cascade that controls directional growth (chemotropism). However, the regulators of chemotropic morphogenesis are ill-defined. By using a non-biased genome-wide screen, we identified hundreds of genes that affect mating. An additional screens identified and validated >20 novel positive and negative regulators of pheromone gradient sensing, chemotropism, shmoo development, and mating. Aside from known regulators of exocytosis and endocytosis, genes involved in translational control downstream of the G-protein-regulated pheromone and filamentous growth MAPK pathways were identified. These include the Scp160 RNA-binding protein and the Asc1, Rpl12b, and Rpl19b ribosomal proteins (RPs). Importantly, we demonstrate that pheromone treatment and G (Gpa1) activation stimulate Scp160 binding to (and inhibition of) Asc1, which acts downstream of glucose-activated G (Gpa2) on the filamentous growth pathway. Moreover, we identify both Rpl12b and Rpl19b as RP paralog-specific positive regulators of translation of mating components, including Scp160. Thus, opposing MAPK pathways may converge at the level of translational control to regulate signaling output. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=165 SRC="FIGDIR/small/422562v2_ufig1.gif" ALT="Figure 1"> View larger version (25K): org.highwire.dtl.DTLVardef@3944e1org.highwire.dtl.DTLVardef@1d9204eorg.highwire.dtl.DTLVardef@1d7e902org.highwire.dtl.DTLVardef@2bfc6_HPS_FORMAT_FIGEXP M_FIG C_FIG
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