Table 1. SMM-sensitive heterozygous deletion mutants.
ORF ID | Gene | SGD Description | Phenotypes |
---|---|---|---|
Transcription | |||
YEL009C | GCN4 | bZIP transcriptional activator of amino acid biosynthetic genes; activator responds to amino acid starvation | M+, E, C, v |
YPR104C | FHL1 | Regulator of ribosomal protein (RP) transcription; has forkhead associated domain that binds phosphorylated proteins; recruits coactivator Ifh1p or corepressor Crf1p to RP gene promoters | M+, C, i |
YBL014C | RRN6 | Component of the core factor (CF) rDNA transcription factor complex; CF is required for transcription of 35S rRNA genes by RNA polymerase I and is composed of Rrn6p, Rrn7p, and Rrn11p | M+, C, i |
YBL005W | PDR3 | Transcriptional activator of the pleiotropic drug resistance network; regulates expression of ATP-binding cassette (ABC) transporters | M+, E, C, v |
YDL020C | RPN4 | Transcription factor that stimulates expression of proteasome genes; Rpn4p levels are in turn regulated by the 26S proteasome in a negative feedback control mechanism; RPN4 is transcriptionally regulated by various stress responses | M+, C, v |
YHR143W-A | RPC10 | RNA polymerase subunit ABC10-α, found in RNA pol I, II, and III | M+, i |
YPL254W | HFI1 | Adaptor protein required for structural integrity of the SAGA complex, a histone acetyltransferase-coactivator complex that is involved in global regulation of gene expression through acetylation and transcription functions | M−, C, v |
YOL148C | SPT20 | Subunit of the SAGA transcriptional regulatory complex | M−, C, va |
YDR145W | TAF12 | Subunit (61/68 kD) of TFIID and SAGA complexes; involved in RNA polymerase II transcription initiation and in chromatin modification, similar to histone H2A | M+, E, C, i |
YBR198C | TAF5 | Subunit (90 kDa) of TFIID and SAGA complexes; involved in RNA polymerase II transcription initiation and in chromatin modification | M+, E, C, i |
YPL129W | TAF14 | Subunit of TFIID, TFIIF, INO80, SWI/SNF, and NuA3 complexes; involved in RNA polymerase II transcription initiation and in chromatin modification | M+, E, C, v |
YMR091C | NPL6 | Component of the RSC chromatin remodeling complex | M+, C, v |
YNR052C | POP2 | RNase of the DEDD superfamily; subunit of the Ccr4-Not complex that mediates 3′–5′ mRNA deadenylation | M−, C, vb |
YBR095C | RXT2 | Component of the histone deacetylase Rpd3L complex | M+, E, C, v |
mRNA processing/export | |||
YDR364C | CDC40 | Pre-mRNA splicing factor | M+, E, C, vb |
YNL004W | HRB1 | Poly(A+) RNA-binding protein; key surveillance factor for the selective export of spliced mRNAs from the nucleus to the cytoplasm | M−, v |
YDR228C | PCF11 | mRNA 3′ end processing factor; essential component of cleavage and polyadenylation factor IA (CF IA), involved in pre-mRNA 3′ end processing and in transcription termination | M+, i |
YMR061W | RNA14 | Component of the cleavage and polyadenylation factor 1 (CF1); CF1, composed of the CF1A complex (Rna14p, Rna15p, Clp1p, Pcf11p) and Hrp1, is involved in cleavage and polyadenylation of mRNA 3′ ends | M−, C, i |
YLR293C | GSP1 | Ran GTPase; GTP binding protein (mammalian Ranp homolog) involved in the maintenance of nuclear organization, RNA processing and transport | M+, C, i |
Translation | |||
YKL009W | MRT4 | Protein involved in mRNA turnover and ribosome assembly | M−, C, v |
YPL143W | RPL33A | Ribosomal 60S subunit protein L33A; nearly identical to RPL33B | M+, E, C, i |
YDR500C | RPL37B | Ribosomal 60S subunit protein L37B; required for processing of 27SB pre-rRNA and formation of stable 66S assembly intermediates; nearly identical to RPL37A | M+, E, C, v |
YDR064W | RPS13 | Protein component of the small (40S) ribosomal subunit | M+, E, i |
YOR182C | RPS30B | Protein component of the small (40S) ribosomal subunit; identical to RPS30A | M+, E, C, v |
YPL090C | RPS6A | Protein component of the small (40S) ribosomal subunit; identical to RPS6B | M−, v |
YOR096W | RPS7A | Protein component of the small (40S) ribosomal subunit; nearly identical to RPS7B | M+, E, C, v |
YPL183W-A | RTC6 | Protein involved in translation; mutants have defects in biogenesis of nuclear ribosomes; sequence similar to prokaryotic ribosomal protein L36 | M−, C, v |
Protein kinase and phosphatase subunits | |||
YER133W | GLC7 | Type 1 S/T protein phosphatase catalytic subunit; cleavage and polyadenylation factor (CPF) component | M+, E, C, i |
YDR028C | REG1 | Regulatory subunit of type 1 protein phosphatase Glc7p | M+, v |
YAR018C | KIN3 | Nonessential serine/threonine protein kinase; possible role in DNA damage response | M−, C, v |
YBL046W | PSY4 | Regulatory subunit of protein phosphatase PP4; presence of Psy4p in the PP4 complex is required for dephosphorylation of the histone variant H2AX during recovery from the DNA damage checkpoint | M+, E, C, v |
Protein degradation | |||
YDR049W | VMS1 | Component of a Cdc48p-complex involved in protein quality control; contributes to ER-associated degradation (ERAD) of specific substrates; forms a mitochondrially-associated complex with Cdc48p and Npl4p under oxidative stress that is required for ubiquitin-mediated mitochondria-associated protein degradation (MAD) | M−, C, v |
YGL116W | CDC20 | Activator of anaphase-promoting complex/cyclosome (APC/C); APC/C is required for metaphase/anaphase transition | M+, E, C, i |
Vacuole/V0 ATPase | |||
YPL234C | VMA11 | Vacuolar ATPase V0 domain subunit c′; involved in proton transport activity; N and C termini are in the vacuolar lumen | M−, C, v |
YHR026W | VMA16 | Subunit c′′ of the vacuolar ATPase; v-ATPase functions in acidification of the vacuole; one of three proteolipid subunits of the V0 domain | M−, C, v |
YEL027W | VMA3 | Proteolipid subunit c of the V0 domain of vacuolar H+ ATPase; required for vacuolar acidification and important for copper and iron metal ion homeostasis | M+, C, v |
YCL005W-A | VMA9 | Vacuolar H+ ATPase subunit e of the V-ATPase V0 subcomplex; essential for vacuolar acidification; involved in V0 biogenesis | M+, va |
Protein trafficking | |||
YDL193W | NUS1 | Forms dehydrodolichyl diphosphate syntase complex with RER2 or SRT1; Nus1p may be involved in protein trafficking | M+, E, C, i |
YDR483W | KRE2 | α1,2-mannosyltransferase of the Golgi; involved in protein mannosylation | M−, C, v |
YBR290W | BSD2 | Heavy metal ion homeostasis protein; facilitates trafficking of Smf1p and Smf2p metal transporters to vacuole where they are degraded; controls metal ion transport, prevents metal hyper-accumulation, functions in copper detoxification | M+, C, v |
Metabolic pathway | |||
YCL009C | ILV6 | Regulatory subunit of acetolactate synthase; acetolactate synthase catalyzes the first step of branched-chain amino acid biosynthesis; enhances activity of the Ilv2p catalytic subunit | M+, v |
YLR303W | MET15 | O-acetyl homoserine-O-acetyl serine sulfhydrylase; required for Methionine and cysteine biosynthesis | M−, v |
YFR055W | IRC7 | β-lyase involved in the production of thiols | M+, v |
YDR531W | CAB1 | Pantothenate kinase, ATP:D-pantothenate 4′-phosphotransferase; catalyzes the first committed step in the universal biosynthetic pathway for synthesis of coenzyme A (CoA) | M−, i |
YJL130C | URA2 | Bifunctional carbamoylphosphate synthetase/aspartate transcarbamylase; catalyzes the first two enzymatic steps in the de novo biosynthesis of pyrimidines | M+, E, v |
YHR128W | FUR1 | Uracil phosphoribosyltransferase; synthesizes UMP from uracil; involved in the pyrimidine salvage pathway | M+, C, i |
Drug resistance | |||
YDR011W | SNQ2 | Plasma membrane ATP-binding cassette (ABC) transporter; multidrug transporter involved in multidrug resistance and resistance to singlet oxygen species | M+, v |
Cytoskeleton | |||
YNR035C | ARC35 | Subunit of the ARP2/3 complex; ARP2/3 is required for the motility and integrity of cortical actin patches | M−, C, i |
YML085C | TUB1 | α-tubulin; associates with β-tubulin (Tub2p) to form tubulin dimer, which polymerizes to form microtubules | M+, C, i |
Amino acid sensor | |||
YNL008C | ASI3 | Subunit of the nuclear inner membrane Asi ubiquitin ligase complex; acts with Asi1p and Asi2p to ensure the fidelity of SPS-sensor signaling | M−, C, v |
YFR029W | PTR3 | Component of the SPS plasma membrane amino acid sensor system; senses external amino acid concentration and transmits intracellular signals that result in regulation of expression of amino acid permease genes | M−, C, i |
Unfolded protein | |||
YJL008C | CCT8 | Subunit of the cytosolic chaperonin Cct ring complex; related to Tcp1p, required for the assembly of actin and tubulins in vivo | M+, C, i |
YJL082W | IML2 | Protein required for clearance of inclusion bodies; localizes to the inclusion bodies formed under protein mis-folding stress | M+, C, v |
YBL075C | SSA3 | ATPase involved in protein folding and the response to stress; plays a role in SRP-dependent cotranslational protein-membrane targeting and translocation | M−, C, v |
Other | |||
YBR156C | SLI15 | Subunit of the conserved chromosomal passenger complex (CPC); complex regulates kinetochore-microtubule attachments, activation of the spindle tension checkpoint, and mitotic spindle disassembly | M+, E, v |
YNL012W | SPO1 | Meiosis-specific prospore protein; required for meiotic spindle pole body duplication and separation | M−, C, v |
YNL013C | YNL013C | Dubious open reading frame; partially overlaps the verified ORF HEF3/YNL014W | M−, C, v |
YER177W | BMH1 | 14-3-3 protein, major isoform; controls proteome at posttranscriptional level, binds proteins and DNA, involved in regulation of exocytosis, vesicle transport, Ras/MAPK and rapamycin-sensitive signaling, aggresome formation, spindle position checkpoint | M−, v |
YGL110C | CUE3 | Protein of unknown function; has a CUE domain that binds ubiquitin, which may facilitate intramolecular monoubiquitination | M−, C, v |
YDR516C | EMI2 | Nonessential protein of unknown function; required for transcriptional induction of the early meiotic-specific transcription factor IME1; required for sporulation | M+, E, v |
YGL168W | HUR1 | Protein of unknown function; reported null mutant phenotype of hydroxyurea sensitivity may be due to effects on overlapping PMR1 gene | M+, E, C, v |
YGR289C | MAL11 | High-affinity maltose transporter (α-glucoside transporter); broad substrate specificity that includes maltotriose | M+, E, C, va |
YBR185C | MBA1 | Membrane-associated mitochondrial ribosome receptor | M−, C, v |
YBR100W | MMS4 | Subunit of structure-specific Mms4p-Mus81p endonuclease; cleaves branched DNA; involved in recombination, DNA repair, and joint molecule formation/resolution during meiotic recombination | M+, E, C, v |
YPL142C | YPL142C | Dubious open reading frame; completely overlaps the verified ORF RPL33A/YPL143W, a component of the large (60S) ribosomal subunit | M+, E, C, i |
YNL028W | YNL028W | Dubious open reading frame; partly overlaps verified ORF KTR5/YNL029C, a putative mannosyltransferase | M−, C, v |
YBR221W-A | YBR221W-A | Putative protein of unknown function; identified by expression profiling and mass spectrometry | M−, v |
YHL015W-A | YHL015W-A | Putative protein of unknown function | M−, v |
YBR196C-A | YBR196C-A | Putative protein of unknown function; identified by fungal homology and RT-PCR | M−, C, v |
YCR061W | YCR061W | Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm in a punctate pattern | M+, C, v |
YBL065W | YBL065W | Dubious open reading frame; partially overlaps verified ORF SEF1/YBL066C; YBL065W is a nonessential gene | M+, E, C, v |
YJR039W | YJR039W | Putative protein of unknown function; the authentic, nontagged protein is detected in highly purified mitochondria in high-throughput studies | M+, E, C, va |
Genes are grouped into general functional categories. SGD descriptions are derived from the Saccharomyces Genome Database. Phenotypes are: M−, Met− (methionine auxotroph); M+, Met+ (methionine prototroph); E, ethionine sensitive (only M+ strains can be tested for ethionine sensitivity); C, canavanine sensitive; i, reported on SGD to be an inviable null mutation in large-scale surveys; v, reported on SGD to be a viable null deletion in large-scale surveys.
Viability not stated on SGD, but the haploid deletion and homozygous null strains exist.
Data in large-scale surveys include both viable and inviable phenotypes. Cells with a deletion of the CDC40 or POP2 genes in the S288C background that BY4743 was derived are viable.