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Glossary of Terms

Selectable Markers

ANR1 anisomycin resistance
CHX1 cycloheximide resistance: Located on Chromosome 1R.
CMP1 mitochondrial chloramphenicol resistance: Previously called Cam or CAR.
FAR 2-fluoroadenosine resistance
GAL1 2-deoxygalactose resistance: Galactokinase mutant located on Chromosome 1R.
HGR1 hygromycin resistance: Located on Chromosome 2L.
MPR1 6-methyl purine resistance: Located on Chromosome 2R.
ORY1 oryzalin resistance
PMR1 paromomycin resistance: Located on Chromosome 2L.
TXS1 paclitaxel (taxol) sensitivity: Wild type is resistant.
VBL1 vinblastine resistance

Alphabetical List of Known Genes

ATU1 alpha tubulin 1
AUX3 unspecified auxotroph: Located on Chromosome 4.
AUX5 unspecified auxotroph: Located on Chromosome 2L.
AUX6 unspecified auxotroph: Located on Chromosome 4L.
AUX8 unspecified auxotroph: Located on Chromosome 4.
AUX9 unspecified auxotroph: Located on Chromosome 4R.
BCD1 broadened cortical domains: Mutation of this gene brings about a broadening of oral and CVP domains. It was originally thought to be non-temperature sensitive, but it is capable of expressing an extreme phenotype at 39 degrees. Homozygotes cannot complete conjugation. Located on Chromosome 3R.
BIG1 big: The mutation increases the size of cells, number of ciliary rows, and size of oral apparatus. Ciliary rows are disorganized, and 10-20% of oral apparatuses are abnormal, with extra membranelles common. Chromosome location is unknown.
BTU1 beta tubulin 1
BTU2 beta tubulin 2
CDAA cell-division-arrest: Temperature-sensitive mutations fail to form a fission zone at 39 degrees, and end up as irregular monsters; originally published as mo1. On Chromosome 4R, localized to a specific macronuclear chromosome.
CDAD cell-division-arrest: Temperature-sensitive mutations cause delayed cell division arrest after shift to 39 degrees; posterior daughter tends to shift anteriorly, forming irregular doublets. Originally published as mo6. Located on chromosome 5.
CDAE cell-division-arrest: Temperature-sensitive mutations cause incomplete fission-zone formation at 39 degrees, with arrest in late-cytokinesis, with the new oral apparatus often abnormal and frequently wedged within the arrested furrow. Originally published as mo8. Chromosome location is unknown.
CDAF cell-division-arrest: Temperature-sensitive mutations cause late fission arrest with failure of subdivision of some ciliary rows (39 degrees); tend to form elongated chains and some monsters. Originally published as mo12. Chromosome location is unknown.
CDAG cell-division-arrest: Temperature-sensitive mutations cause late fission arrest and varied membranellar abnormalities at 39-40 degrees. Pleiotropic and incompletely penetrant. Chromosome location is unknown.
CDAH cell-division-arrest: Temperature-sensitive mutations cause fission block, and at an extreme a failure to form a fission zone, with anterior migration of the oral primordium within a sub-surface vesicle (39 degrees). Located on chromosome 5.
CDAI cell-division-arrest: Temperature-sensitive mutations cause unequal fission-arrest ("hammer-head") following an anterior sliding of the oral primordium on the cell surface (at 39 degrees). Chromosome location is unknown.
CDAK cell-division-arrest: This temperature-sensitive mutation causes an unequal fission-arrest with a diagonal and incomplete fission zone, leading to a much smaller anterior daughter, usually arrested in fission. Chromosome location is unknown.
CHP1 temperature sensitive cell cycle, heat shock, and phosphorylation defect: Defective in heat shock response
CNA1 centromere associated H3 histone
CON1 conical cell shape: The mutation brings about conical phenootype with broad posterior end; oral primordium forms near the posterior end of the cell, and the posterior daughter cell is smaller than the anterior daughter. In a mixed D/B strain genetic background. Originally published as co. Located on Chromosome 4L.
CON2 conical cell shape: The mutation brings about conical cell shape; expression slightly more pronounced at 39 degrees than at 28 degrees. Division products are equal in size. Chromosome location is unknown.
DBL1 doublet-former: The mutation causes variable proclivity to form regular homopolar doublets. Penetrance is highly variable. Chromosome location is unknown.
DCC1 defective in ciliogenesis and cytokinesis: Temperature sensitive mutation
DISA disorganized cortex: The mutation brings about a disorganization of ciliary rows that is more extreme the higher the temperature; cell division nonetheless is nearly normal. Located on Chromosome 5.
DISD disorganized cortex: The mutation brings about disorganized ciliary rows at 39-40 degrees C; also reduced number of ciliary rows. Chromosome location is unknown.
DOA2 defective oral apparatus: The temperature-sensitive mutation causes gradual degeneration of the oral apparatus, frequent oral replacement, rounding of the cell, and division blockage at 39 degrees. Chromosome location is unknown.
DRH1 dicer related helicase
DYH6 dynein heavy chain 6
DYH7 dynein heavy chain 7
ELO1 elongated: Mutant cells are elongated, with unequal cell division yielding smaller posterior division products. The phenotype is evident at 28 degrees but more extreme at 39 degrees. Chromosome location is unknown.
ENJ1 enhancer of janus: Located on Chromosome 3.
EXO1 secretory mutant: Located on Chromosome 5.
EXO3 secretory mutant: Located on Chromosome 3.
EXOA1 secretory mutant: Located on Chromosome 4L.
EXOB1 secretory mutant: Located on Chromosome 4L.
FAT2 fat cell body: Formerly known as FATB. Mutants are somewhat pudgy but otherwise completely normal. Chromosome location is unknown.
FAT4 fat cell body: Formerly known as FATD. Mutants have a rounded cell shape, but otherwise completely normal. Located on chromosome 5.
FER1 iron requiring auxotroph: Located on Chromosome 4R.
GFP green fluorescent protein
GPCR3 G protein-coupled receptor 3
GPCR6 G protein-coupled receptor 6
GPCR8 G protein-coupled receptor 8
GTU1 gamma tubulin 1
HHO1 histone H1
HHT1 histone H3.1
HHT2 histone H3.2
HHT3 histone H3.3
HHT4 histone H3.4
HMGB high mobility group B
HMGC high mobility group C
HPO1 hypoangular: These mutations bring about a complex phenotype with contractive vacuole pores abnormally close to the oral apparatus, and clockwise slippage of oral primordia. Other patterning defects appear at high temperature: hpo1-1 and hpo1-4 have weak expression at 28 degrees and very strong expression at 39 degrees; hpo1-2 and hpo1-3 have moderate expression at 28 degrees and somewhat stronger expression at 39 degrees. hpo1-1 originally published as hpo1; hpo1-2 originally published as hpo2; hpo1-3 originally published as hpo3. Located on Chromosome 3R.
HTA3 histone H2A.Z: Also called histone hv1.
HTAY histone H2A.Y
JANA janus: These mutations brings a "janus" phenotype to expression, with partially reversed oral apparatus on the dorsal surface and two contractile-vacuole pore sets on one side of the cell. Flattened cell shape. Not temperature sensitive. Depends on a gene-specific enhancer (enjA) for maximal expression. Homozygotes cannot complere conjugation. janA-1 originally published as jan. Located on Chromosome 3R.
JANB janus: The temperature-sensitive mutation expresses a "janus" phenotype: partially reversed oral apparatus on the dorsal surface; two contractile-vacuole pore sets. Located on Chromosome 2.
JANC janus: Mutations bring about a strong "janus" phenotype: partially reversed oral apparatus on the dorsal surface; two contractile-vacuole pore sets. Flattened cell shape. Not temperature sensitive. Homozygotes can complere conjugation normally., Located on Chromosome 1R.
LKN1 low kinety (ciliary-row) number: Mutations bring about thinner cells with a reduced number of ciliary rows combined with a reduced fidelity in transmission of pre-existing row numbers, probably owing to interruptions and irregularities in the rows. Chromosome location is unknown.
MAT1 mating type potentialities: Located on Chromosome 2L.
MLH micronucleus linker histone
MPC altered membranellar-pattern: Mutations cause the formation of a fourth membranelle in the oral apparatus. Penetrance is higher at 39 degrees than at 28 degrees. Located on Chromosome 3L.
MPD altered membranellar-pattern: Mutations express a temperature-sensitive formation of four or five well-formed membranelles in the oral apparatus. The cells become long and slender. Located on Chromosome 3R.
MPF altered membranellar-pattern: The temperature-sensitive mutation results in short and multiple membranelles, and a characteritically shortened undulating membrane, all expressed at restrictive temperature (39 degrees) only. Chromosome location is unknown.
MPG altered membranellar-pattern: The mutation brings about a "trihymena" form, with non-conditional formation of two instead of three membranelles in the oral apparatus. Located on Chromosome 4.
MPH altered membranellar-pattern: The mutation brings about a "trihymena" form, with non-conditional formation of two instead of three membranelles in the oral apparatus, at a somewhat lower frequency than mpG-1. Chromosome location is unknown.
MTT1 Cd-inducible metallothionein gene
MTT2 Cu-inducible metallothionein gene
MUM1 misaligned undulating membrane: The mutation shows non-temperature-sensitive fragmentation of the undulating membrane. Chromosome location is unknown.
OAD1 outer arm deficient: Temperature sensitive mutation affecting assembly of the outer dynein arm into cilia.
PDD2 programmed DNA degradation protein 2
PDD3 programmed DNA degradation protein 3
PIG4 tyrosine dependent pigment producer: Located on Chromosome 3.
PSMA pseudomacrostome: Mutations bring about an elongated phenotype with development of large oral-replacement or misplaced cell division oral primordia. All alleles are temperature sensitive, but to varying degrees. Located on chromosome 5.
PSMB pseudomacrostome: The pleiotropic temperature sensitive mutation brings about an elongated phenotype with development of large oral-replacement or misplaced pre-cell-division oral primordia, with smaller posterior daughter cells. Lower penetrance than psmA1 and psmA3. Located on Chromosome 4L.
RMM1 cis-acting elements affecting control of rDNA replication: Located on Chromosome 2L.
RSEB1 immobilization antigen regulator: Located on Chromosome 5.
RSEC1 immobilization antigen regulator: Located on Chromosome 4L.
RSED1 immobilization antigen regulator: Located on Chromosome 5.
SCR1 screwy: The mutation causes ciliary rows to be helically wound around the cell. Chromosome location is unknown. This gene was published under the name TWI1, and later renamed SCR1 to avoid confusion with the piwi-homologue that had previously been named TWI1.
SERH1 immobilization antigen structural locus: Located on Chromosome 4L.
SQT1 squat: The mutant is shortened, with an ovoid shape. Not temperature-sensitive. Chromosome location is unknown.
THY1 thymidine auxotroph: Located on Chromosome 1.
TS10 temperature sensitive: Located on Chromosome 5.
TS101 temperature sensitive: Located on Chromosome 1R.
TS102 temperature sensitive: Located on Chromosome 3L.
TS103 temperature sensitive: Located on Chromosome 3R.
TS104 temperature sensitive: Located on Chromosome 3R.
TS105 temperature sensitive: Located on Chromosome 5.
TS106 temperature sensitive: Located on Chromosome 3.
TS107 temperature sensitive: Located on Chromosome 5.
TS108 temperature sensitive: Located on Chromosome 5.
TS109 temperature sensitive: Located on Chromosome 5.
TS11 temperature sensitive: Located on Chromosome 4R.
TS11 temperature sensitive: Located on Chromosome 5.
TS110 temperature sensitive: Located on Chromosome 5.
TS112 temperature sensitive: Located on Chromosome 5.
TS114 temperature sensitive: Located on Chromosome 5.
TS12 temperature sensitive: Located on Chromosome 1.
TS14 temperature sensitive: Located on Chromosome 1R.
TS15 temperature sensitive: Located on Chromosome 5.
TS16 temperature sensitive: Located on Chromosome 4.
TS17 temperature sensitive: Located on Chromosome 1R.
TS18 temperature sensitive: Located on Chromosome 4.
TS19 temperature sensitive: Located on Chromosome 5.
TS20 temperature sensitive: Located on Chromosome 1.
TS21 temperature sensitive: Located on Chromosome 3L.
TS22 temperature sensitive: Located on Chromosome 1.
TS23 temperature sensitive: Located on Chromosome 5.
TS24 temperature sensitive: Located on Chromosome 5.
TS25 temperature sensitive: Located on Chromosome 1.
TS26 temperature sensitive: Located on Chromosome 5.
TS27 temperature sensitive: Located on Chromosome 5.
TS28 temperature sensitive: Located on Chromosome 1.
TS29 temperature sensitive: Located on Chromosome 2L.
TS30 temperature sensitive: Located on Chromosome 5.
TS32 temperature sensitive: Located on Chromosome 3R.
TS33 temperature sensitive: Located on Chromosome 3R.
TS34 temperature sensitive: Located on Chromosome 3R.
TS35 temperature sensitive: Located on Chromosome 2.
TS36 temperature sensitive: Located on Chromosome 2.
TS37 temperature sensitive: Located on Chromosome 2.
TS38 temperature sensitive: Located on Chromosome 2.
TS39 temperature sensitive: Located on Chromosome 2.
TS5 temperature sensitive: Located on Chromosome 1.
TS6 temperature sensitive: Located on Chromosome 1R.
TS7 temperature sensitive: Located on Chromosome 2L.
TS8 temperature sensitive: Located on Chromosome 2L.
TS9 temperature sensitive: Located on Chromosome 4.
TSA1 temperature sensitive: Located on Chromosome 3R.
TYR10 tyrosine auxotroph: Located on Chromosome 1.
TYR14 tyrosine auxotroph: Located on Chromosome 1.
TYR19 tyrosine auxotroph: Located on Chromosome 1.
TYR9 tyrosine auxotroph: Located on Chromosome 1.
TYRA tyrosine auxotroph: Located on Chromosome 2L.
TYRB tyrosine auxotroph: May be deficient in unconjugated pteridine biosynthesis. Located on Chromosome 2R.
TYRC tyrosine auxotroph: Deficient in phenylalanine hydroxylase. Located on Chromosome 4L.
TYRD tyrosine auxotroph: May be deficient in unconjugated pteridine biosynthesis. Located on Chromosome 2L.
TYRE tyrosine auxotroph: Located on Chromosome 1.
UBC2 E2 ubiquitin-conjugating enzyme