[No authors listed]
RSC (Remodel the Structure of Chromatin) is an ATP-dependent chromatin remodeling complex essential for the growth of Saccharomyces cerevisiae. RSC exists as two distinct isoforms that share core subunits including the ATPase subunit Nps1/Sth1 but contain either Rsc1or Rsc2. Using the synthetic genetic array (SGA) of the non-essential null mutation method, we screened for mutations exhibiting synthetic growth defects in combination with the temperature-sensitive mutant, nps1-105, and found connections between mitochondrial function and RSC. rsc mutants, including rsc1Î, rsc2Î, and nps1-13, another temperature-sensitive nps1 mutant, exhibited defective respiratory growth; in addition, rsc2Î and nps1-13 contained aggregated mitochondria. The rsc2Î phenotypes were relieved by RSC1 overexpression, indicating that the isoforms play a redundant role in respiratory growth. Genome-wide expression analysis in nps1-13 under respiratory conditions suggested that RSC regulates the transcription of some target genes of the HAP complex, a transcriptional activator of respiratory gene expression. Nps1 physically interacted with Hap4, the transcriptional activator moiety of the HAP complex, and overexpression of HAP4 alleviated respiratory defects in nps1-13, suggesting that RSC plays pivotal roles in mitochondrial gene expression and shares a set of target genes with the HAP complex.
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STP22, MRPL32, BUD23, TUP1, LOC1, SNF7, AAT2, RIC1, MEF1, BUD20, VPS34, MAP1, RSC2, ATG17, MRPL4, GCV3, GGC1, NUP84, RPL31A, SIT4, REG1, RGP1, LSM6, KRE28, RTG3, SHP1, VMA2, FZO1, AIM4, PDB1, MRPS5, MRPL27, RTG2, RSC1, CCM1, NSR1, TIF4631, BUB1, ELP2, EFG1, RCY1, RPL39, SET2, RPB4, ARG2, RPA12, VPS25, SOD1, RSM7, MGM101, EAP1, VPH2, HAP4, DBP7, RTG1, IDH2, ARP8, HNT3, YOR302W, STH1, MRS1, NPL6, RPL13B, PPA2, LSM7, YDJ1, ARP5, MRP7, CSE2, RSM19, POS5, BEM4, MSY1, VPS28, SNF8, MSF1, MRPL51, SNT309, ARN2, RPL27A, RPS27B, VMA22, CTF8, VMA3
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