Table 2.
Gene name | Screen, criteria | Important for | Description |
---|---|---|---|
ARG82 | U,2 | AA metabolism | Inositol polyphosphate multikinase |
ERV46 | U,1,4,5 | Cargo transport | ER vesicle protein, component of COPII complex; required for membrane fusion |
HIS1 | U,1,4,5 | AA metabolism | ATP phosphoribosyltransferase |
UGA1 | U,5 | AA metabolism | Gamma‐aminobutyrate (GABA) transaminase |
SLA1 | U,2,3 | Actin binding | Cytoskeletal protein binding protein; required for assembly of the cortical actin cytoskeleton |
SAP155 | K,2,3,5 | Cell cycle | Protein required for function of the Sit4 protein phosphatase |
YER068C‐A | U,5 | Dubious open reading frame | Dubious open reading frame/overlaps with ARG5, ARG6 acetylglutamate kinase and N‐acetyl‐gamma‐glutamyl‐phosphate reductase |
YIL032C | U,5 | Dubious open reading frame | Dubious open reading frame/next to BCY1 |
ERG3 | U,1,5 | Ergosterol biosynthesis | C‐5 sterol desaturase |
GAL83 | K,1 | Glucose repression | One of three possible beta‐subunits of the Snf1 kinase complex |
GUP1 | U,2,3 | Glycerol metabolism, protein folding | Plasma membrane protein involved in remodeling GPI anchors |
PPZ1 | K,5 | Ion homeostasis | Serine/threonine protein phosphatase Z, isoform of Ppz2p; involved in regulation of potassium transport, which affects osmotic stability, cell cycle progression, and halotolerance |
FUS1 | U,5 | Mating | Membrane protein localized to the shmoo tip |
AAT2 | U,5 | Metabolism | Cytosolic aspartate aminotransferase involved in nitrogen metabolism |
PTC6 | K,2,3 | Metabolism | Mitochondrial type 2C protein phosphatase (PP2C) |
GIM4 | U,5 | Microtubule chaperone/Protein folding | Subunit of the heterohexameric cochaperone prefoldin complex |
PAC10
GIM2 |
U,5 | Microtubule chaperone/Protein folding | Subunit of the heterohexameric cochaperone prefoldin complex |
BIM1 | U,4,5 | Microtubule end binding | Microtubule plus‐end‐binding protein |
MSH1 | U,5 | Mitochondrial homeostasis | Escherichia coli MutS homolog, binds DNA mismatches, required for mitochondrial function |
BUB1 | K,4,5 | Mitosis | Protein kinase required for cell cycle checkpoint, delays entry into anaphase until kinetochores bound by opposing microtubules |
ELM1 | K,2 | Morphogenesis | Serine/threonine protein kinase that regulates cellular morphogenesis |
HSL1 | K,2 | Morphogenesis | Nim1‐related protein kinase; regulates the morphogenesis and septin checkpoints |
NUP60 | U,5 | Nuclear transport | FG‐nucleoporin component of central core of the nuclear pore complex |
SXM1 | U,4,5 | Nuclear transport | Nuclear transport factor (karyopherin) |
CBR1 | U,5 | Respiration | Microsomal cytochrome β reductase |
RTC3 | U,4,5 | RNA metabolism | Protein of unknown function involved in RNA metabolism |
CKA1 | U,1,4,5 | Signaling | Alpha catalytic subunit of casein kinase 2 (CK2) |
CKB1 | U,5 | Signaling | Beta regulatory subunit of casein kinase 2 (CK2) |
CKB2 | K,1 | Signaling | Beta' regulatory subunit of casein kinase 2 (CK2) |
FUS3 | K,3,5 | Signaling | Mitogen‐activated serine/threonine protein kinase (MAPK), part of PRS |
HOG1 | K,3 | Signaling | Mitogen‐activated protein kinase involved in High Osmolarity (HOG) pathway |
KSS1 | K,3 | Signaling | Mitogen‐activated protein kinase (MAPK); functions in PRS and signal transduction pathways that control filamentous growth and pheromone response |
PBS2 | K,5 | Signaling | MAP kinase kinase of the HOG signaling pathway |
SSK2 | K,3 | Signaling | MAP kinase kinase kinase of HOG1 signaling pathway |
FAR1 | U,1 | Signaling/cell cycle/polarization | CDK inhibitor, nuclear anchor, recruited by Ste18‐Ste4 at polarity patch |
SIP1 | U,4,5 | Signaling/glucose repression | Alternate beta‐subunit of the Snf1 protein kinase complex |
KAR4 | U,5 | Signaling/mating | Transcription factor required for activation of some pheromone‐responsive genes |
STE50 | U,1,4 | Signaling/mating | Adaptor protein, in PRS helps connect Ste20 MAPKKKK to Ste11 MAPKKK |
SKY1 | K,3 | Splicing | SR protein kinase (SRPK); varied functions, regulates proteins involved in mRNA metabolism and cation homeostasis, helps some LexA fusion proteins bind operator |
KIN3 | K,5 | Stress | Non‐essential serine/threonine protein kinase; possible role in DNA damage response |
OCA1 | K,1 | Stress | Protein tyrosine phosphatase; required for cell cycle arrest in response to oxidative damage of DNA |
CTK1 | K,4 | Transcription regulation | Catalytic (alpha) subunit of C‐terminal domain kinase I (CTDK‐I); phosphorylates RNA pol II |
DEP1 | U,5 | Transcription regulation | Component of the Rpd3L histone deacetylase complex, variously needed for activation and repression, regulates DNA replication origin timing |
SUM1 | U,2,4,5 | Transcription regulation | Transcriptional repressor that regulates middle‐sporulation genes; required for mitotic repression of middle‐sporulation‐specific genes; also acts as general replication initiation factor; involved in telomere maintenance, chromatin silencing |
SWI5 | U,5 | Transcription regulation | Part of Mediator and Swi/Snf nucleosome remodeling complexes |
UME6 | U,4,5 | Transcription regulation | Meiotic transcription regulator, DNA binding, recruits variously Sin3/Rpd3 repressor (HDAC) and Ime1 activator. |
RPL12A | U,1,4 | Translation | Ribosomal 60S subunit protein L12A |
RPL19B | U,1,4,5 | Translation | Ribosomal 60S subunit protein L19B |
RPL34A | U,4,5 | Translation | Ribosomal 60S subunit protein L34A |
ECM15 | U,1,4,5 | Unknown | Possibly tetrameric, non‐essential protein, unknown function |
VPS64 | U,5 | Vacuole metabolism | Required for cytoplasmic proteins to enter vacuole |
Selection criteria codes (see Fig 2A–C): (1) O(0.6 nM) < 3.39; (2) O(0.6 nM) > 7.72; (3) η2(P(0.6 nM)) < 0.027; (4) η2(P(0.6 nM)) > 0.054; (5) η2(P(20 nM)) > 0.019. Genes from the strains in the unbiased (U) screen and the strains in the non‐essential kinase and phosphatase screen (K) screen that showed altered PRS system output (O), low or high pathway variability (η2(P)) at low pheromone (0.6 nM), or high variability (η2(P)) at high dose (20 nM). Table shows gene name, screen from which it was selected and selection criteria, overall functional class, and a brief description of its molecular role or activity.