FGSC #9475

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Reporting Genes: A ^m99 un-3 nic-2 ad-3B cyh-1

Species: crassa

Allele: m99, 2-17-814, 43002, KH52

Alternate Strain Number: 1848

Depositor: DDP

Linkage Group: IL

Mating Type: A

Species Number: 10

ref1: Saupe et al 1996 MGG 250:115-122, https://doi.org/10.1007/bf02191831

Deposit Sheet ↗

Genes

Locus	Cultural Requirements	Link Group	Type
A^m99	IL. Between un-3 (0.04 to 0.1%) and un-16 ( < 1%) (488, 758; D. D. Perkins, unpublished data). (609) Opposite mating types are essential for a complex of events associated with sexual reproduction and morphogenesis: attraction of trichogyne to cells of opposite mating type (39, 93); pickup and transport of the nucleus to the ascogonium; growth and development of the perithecium; proliferation of heterokaryotic ascogenous hyphae; conjugate nuclear divisions in precrozier and crozier cells; karyogamy. Mating type alleles also act as vegetative incompatibility genes during the vegetative phase. A+a combinations are unable to form stable heterokaryons (66, 384, 830, 914). Vegetative fusion is usually followed by cell death (384), but some A+a heterokaryons grow slowly (252, 412, 422). Heterozygous A/a duplications are highly abnormal, with inhibited growth and spider-like morphology (761. 804). Incompatibility in heterokaryons or duplications is relieved by spontaneous deletion of either allele (252, 756). Vegetative incompatibility is not expressed during the sexual phase after fertilization. Both manifestations of vegetative incompatibility are suppressed by tol, but sexual compatibility is not affected (755). The vegetative incompatibility is normally suppressed in N. tetrasperma (668) and N. sitophila (674, 804). Extensive efforts have failed to separate the sexual and vegetative traits by genetic recombination (758). Null mutants selected by loss of vegetative incompatibility usually lose both sexual and vegetative functions simultaneously (one exception), and both functions are usually restored simultaneously in revertants selected for restoration of fertility (one null mutant gives atypical revertants) (252, 411, 412).Only two mating type alleles, A and a, are known. These are apparently homologous throughout the genus Neurospora (820) and perhaps in related genera (770). Nothing is known about the genetics of the five true-homothallic species of Neurospora, which closely resemble N. crassa in karyotype and meiotic behavior, including the fusion of two haploid nuclei in the penultimate cell of the crozier to form the zygote nucleus (855). In the early literature, A was called + (plus) or A, and a was called - (minus) or B (e.g., reference 286). The locus may also be designated mt, mating type (e.g., reference 808), and is usually referred to as mt in the present paper.	IL	B
ad-3B	IR. Between ad-3A (0.1 to 0.7%) and nic-2 (3%) (271). (482) Uses adenine or hypoxanthine (682). Blocked in interconversion of AIR to CAIR (348) (Fig. 8). Produces purple pigment, permitting direct visual selection (276, 682). Pigment is secreted with low concentrations of adenine (e.g., 0.1 mM), not with high concentrations (2 mM) (276, 682, 785). Pigment production used to assess effect of histidine and tryptophan on purine nucleotide synthesis (786). Reduced interallelic fertility (264, 407). Complementation maps (268, 274). Relation of mutagens to complementation patterns (269). Mutants with non-polarized complementation patterns on the right side of the complementation map grow on minimal medium if supplied with CO2; other mutants do not respond to CO2, (270). Used extensively for mutagenesis (see ad-3A). Rearrangement T(I- >III)Y112M4i ad-3B, which has a breakpoint inseparable from ad-3B, was the first insertional translocation to be reported for fungi (266). Allele 7-017-0137 shows "fixed instability," mutating to an unstable prototrophic allele (41). Alleles 2-17-126, 12-21-28, and numerous others are supersuppressible (408, 749, 955). Called complementation group B.	IR	B
cyh-1	IR. Right of nit-1 (6%). Left of T(STL76) and al-2 (8 to 13%) (496, 797, 808).Resistant to cycloheximide (496, 748). Resistance is recessive in duplications (1090). Dominance reported in forced heterokaryons (496, 748) may have been due to skewed nuclear ratios (1090). Protein synthesis on ribosomes of the mutant cyh-1 proceeds in the presence of cycloheximide in a cell-free system (834). Readily scored on slants with 10 µg of cycloheximide per ml autoclaved in the medium. Excellent as a marker and valuable for selecting somatic recombinants or deletions in heterozygous duplications (748, 1091). Used to show that the cycloheximide-induced phase shift of the circadian clock involves protein synthesis (738). Called act-1: actidione resistant-1.	IR	B
nic-2	IR. Between ad-3B (4%) and ace-7 (4 to 7%) (271, 578). (482) Grows on nicotinic acid, nicotinamide, or high concentrations of quinolinic acid (97, 1168). Cannot use kynurenine, hydroxykynurenine, or hydroxyanthranilic acid (96, 1168). Accumulates 3-hydroxyanthranilic acid (96) (Fig. 18). Aging cultures accumulate red-brown pigment in the medium. Used to study intralocus recombination (908). Translocations T(4540) and T(S1325)are inseparable from nic-2 (808, 908, 911).	IR	B
un-3	IL. Right of In(NM176); hence, right of ser-3 (1%) (1093). Left of mt(0.04 to 0.1%) (488, 758). Closest bracketing marker left of mt (482). Unknown function. Heat sensitive (484). Growth drops off sharply between 28.5°C and 30°C (R.L. Metzenberg, personal communication). Multiply transport deficient at permissive temperatures with increased fragility of protoplasts (543); reduced rate of uptake of citrulline (1075) and aspartate (543, 1149). Resistant to ethionine and to p-fluorophenylalanine at 25°C (542, 543). Used to tag mating type (487) and as a flanker in an attempt to resolve the mating type region by recombination (758). Strains with probable un-3alleles are selected as citrulline-resistant mutants of pyr-3 arg-12s; most mutants selected in this way show complementation between alleles (1075). A possible functional relation to mating type is discussed in reference 543, Growth at 25°C aided by 0.3 mg of sodium acetate per ml. May be scored by slow growth at 25°C if acetate is not added to minimal medium (487). Formerly called un(55701).	IL	B