TABLE 2:
Candidate genes on chromosome XIV. Continued
Systematic name | Standard name | Hit from UPRE::GFP screen? (Jonikas et al., 2009) | Z-score from 25°C HSE::GFP screen (Brandman et al., 2012) | SGD gene description |
---|---|---|---|---|
YNL148C | ALF1 | Yes | 0.59263 | Alpha-tubulin folding protein; similar to mammalian cofactor B; Alf1p-GFP localizes to cytoplasmic microtubules; required for the folding of alpha-tubulin and may play an additional role in microtubule maintenance |
YNL077W | APJ1 | No | –0.011564 | Hsp40 chaperone with a role in SUMO-mediated protein degradation; works in concert with Hsp70 and Hsp110 (Sse1p) to promote disaggregation of intranuclear protein inclusions; competes with Hsp104 in disaggregation, supporting turnover instead of refolding; member of DnaJ-like family, conserved across eukaryotes; overexpression interferes with propagation of the [Psi+] prion; forms nuclear foci upon DNA replication stress |
YNL159C | ASI2 | No | 0.198189 | Subunit of the INM Asi ubiquitin ligase complex; the Asi complex targets both misfolded proteins of the INMAD pathway and inner for ubiquitin-mediated degradation; acts with Asi1p and Asi3p to ensure the fidelity of SPS-sensor signaling by targeting latent unprocessed forms of Stp1p and Stp2p, maintaining the repressed state of gene expression in the absence of inducing amino acids |
YNL008C | ASI3 | No | –0.071735 | Subunit of the INM Asi ubiquitin ligase complex; Asi complex targets both misfolded proteins of the INMAD pathway and regulators of sterol biosynthesis for ubiquitin-mediated degradation; acts with Asi1p and Asi2p to ensure the fidelity of SPS-sensor signaling by targeting latent unprocessed forms of Stp1p and Stp2p, maintaining the repressed state of gene expression in the absence of inducing amino acids |
YNL242W | ATG2 | No | 0.171614 | Peripheral membrane protein required for autophagic vesicle formation; also required for vesicle formation during pexophagy and the cytoplasm-to-vaucole targeting (Cvt) pathway; involved in Atg9p cycling between the phagophore assembly site and mitochondria; contains an APT1 domain that binds phosphatidylinositol-3-phosphate; essential for cell cycle progression from G2/M to G1 under nitrogen starvation; forms cytoplasmic foci upon DNA replication stress |
YNR007C | ATG3 | No | –0.16644 | E2-like enzyme; involved in autophagy and cytoplasm-to-vacuole targeting (Cvt) pathway; plays a role in formation of Atg8p-phosphatidylethanolamine conjugates, which are involved in membrane dynamics during autophagy and Cvt; interaction with Atg8p regulated by acetylation by NuA4 histone acetyltransferase Esa1p while attenuation of Atg3 acetylation is mediated by histone deacetylase Rpd3p; Atg12p-Atg5p conjugate enhances E2 activity of Atg3p by rearranging its catalytic site |
YNL223W | ATG4 | No | 0.287679 | Conserved cysteine protease required for autophagy; cleaves Atg8p to a form required for autophagosome and Cvt vesicle generation |
YNR051C | BRE5 | Yes | –0.326932 | Ubiquitin-protease cofactor; forms deubiquitination complex with Ubp3p that coregulates anterograde and retrograde transport between the ER and Golgi compartments, deubiquitinating COPII and COPI vesicle coat constituents, Sec23p and Sec27p; involved along with Ubp3p in the steady-state retention of Golgi membrane proteins, such as glycosyltransferases; null is sensitive to brefeldin A |
YNL155W | CUZ1 | No | 0.275969 | Protein with a role in the ubiquitin-proteasome pathway; interacts with ubiquitinated protein, Cdc48p, and the proteasomal regulatory particle; may protect cells from trivalent metalloid–induced proteotoxicity; contains a PACE promoter element and is coregulated with proteasome subunit genes; AN1-type zinc finger protein, with DHHC and ubiquitin-like domains (UBL); orthologue of ZFAND1, a human gene linked to cancer; protein abundance increases under DNA replication stress |
YNL001W | DOM34 | No | -–.374767 | Protein that facilitates ribosomal subunit dissociation; Dom34-Hbs1 complex and Rli1p have roles in dissociating inactive ribosomes to facilitate translation restart, particularly ribosomes stalled in 3′ UTRs; required for RNA cleavage in no-go decay, but reports conflict on endonuclease activity; pelota orthologue; protein abundance increases in response to DNA replication stress; DOM34 has a paralogue, YCL001W-B, that arose from the whole-genome duplication |
YNL080C | EOS1 | Yes | 1.454465 | Protein involved in N-glycosylation; deletion mutation confers sensitivity to oxidative stress and shows synthetic lethality with mutations in the spindle checkpoint genes BUB3 and MAD1; YNL080C is not an essential gene |
YNL281W | HCH1 | No | 0.288015 | Heat shock protein regulator; binds to Hsp90p and may stimulate ATPase activity; originally identified as a high-copy-number suppressor of a HSP90 loss-of-function mutation; role in regulating Hsp90 inhibitor drug sensitivity; GFP-fusion protein localizes to the cytoplasm and nucleus; protein abundance increases in response to DNA replication stress |
YNL227C | JJJ1 | Yes | –0.24319 | Cochaperone that stimulates the ATPase activity of Ssa1p; required for a late step of ribosome biogenesis; associated with the cytosolic large ribosomal subunit; contains a J-domain; mutation causes defects in fluid-phase endocytosis |
YNL123W | NMA111 | No | –0.143379 | Serine protease and general molecular chaperone; cleaves Roq1p, which modifies the substrate specificity of the Ubr1p Ub-ligase, promoting the stress-induced homeostatically regulated protein degradation (SHRED) of misfolded and native ER-membrane and cytosolic proteins; chaperone activity involved in the heat stress response; promotes apoptosis through proteolysis of Bir1p; role in lipid homeostasis; mammalian Omi/HtrA2 serine protease family member |
YNL149C | PGA2 | N/a | N/a | Essential protein required for maturation of Gas1p and Pho8p; involved in protein trafficking; GFP-fusion protein localizes to the ER and YFP-fusion protein to the nuclear envelope-ER network; null mutants have a cell separation defect |
YNL097C | PHO23 | Yes | –0.899301 | Component of the Rpd3L histone deacetylase complex; involved in transcriptional regulation of PHO5; affects termination of snoRNAs and cryptic unstable transcripts (CUTs); C-terminus shares significant sequence identity with the human candidate tumor suppressor p33-ING1 and its isoform ING3 |
YNL206C | RTT106 | Yes | 1.472194 | Histone chaperone; involved in regulation of chromatin structure in both transcribed and silenced chromosomal regions; affects transcriptional elongation; has a role in regulation of Ty1 transposition; interacts physically and functionally with Chromatin Assembly Factor-1 (CAF-1) |
YNL007C | SIS1 | n/a | 0.391894 | Type II HSP40 cochaperone that interacts with the HSP70 protein Ssa1p; shuttles between cytosol and nucleus; mediates delivery of misfolded proteins into the nucleus for degradation; involved in proteasomal degradation of misfolded cytosolic proteins; protein abundance increases in response to DNA replication stress; polyQ aggregates sequester Sis1p and interfere with clearance of misfolded proteins; similar to bacterial DnaJ proteins and mammalian DnaJB1 |
YNL209W | SSB2 | No | 0.211499 | Cytoplasmic ATPase that is a ribosome-associated molecular chaperone; functions with J-protein partner Zuo1p; may be involved in the folding of newly synthesized polypeptide chains; member of the HSP70 family; SSB2 has a paralogue, SSB1, that arose from the whole-genome duplication |
YNL064C | YDJ1 | No | 1.879207 | Type I HSP40 cochaperone; involved in regulation of HSP90 and HSP70 functions; acts as an adaptor that helps Rsp5p recognize cytosolic misfolded proteins for ubiquitination after heat shock; critical for determining cell size at Start as a function of growth rate; involved in protein translocation across membranes; member of the DnaJ family; chimeric protein in which the human p58IPK J domain replaces yeast Ydj1p J domain can complement yeast ydj1 mutant |