FGSC #2990

Mutant Type

Genus: N

reporting_genes: Ban mei-3;inl

species: Neurospora crassa

allele: N452P63 N289;89601

stock: 473 (DDP)

glasgow:

mutagen: S

Depositor: DNP

Link Group: IL IL;VR

MT: a

Species No: 10

gene_back: M

oppmt: 0

trans:

ref1: https://doi.org/10.1016/S0147-5975(77)80040-6

ref2:

site:

country:

ksudc_link: https://digital.lib.k-state.edu/item/neurospora-crassa/fgsc-2990

ksudc_link_html: https://digital.lib.k-state.edu/item/neurospora-crassa/fgsc-2990 ↗

Genes

Locus	Cultural Requirements	Link Group	Type
Ban	IL. Left of mat (14%), Probably left of leu-3. Each ascus delimits a single giant ascospore enclosing all four meiotic products and their mitotic derivatives. Morphology is abnormal, with short aerial hyphae and no protoperithecia.	IL	B
inl	VR. Between pho-3 (3 to 4%) and pab-1 (1 to 10%). Right of al-3 (362, 397, 1036). (482)Requires inositol (65). Lacks D-myoinositol-1-phosphatase (1142). Lack of glucocycloaldolase found by Pina and Tatum (826) is attributed by Williams (1142) to drastic repression of glucocycloaldolase by the concentration of inositol used for growth. Growth is colonial on low levels of inositol (367). Tends to extrude dark pigment into the medium when grown on suboptimal inositol. Composition of phospholipids and cell walls is abnormal on limiting inositol (367, 439, 440, 501). Inhibited by hexachlorocyclohexane (366, 457, 931). Conidia are subject to death by unbalanced growth on minimal medium (1028, 1033), a property exploited for mutant enrichment ("inositol-less death") (606, 647) because double mutants are at a selective advantage. Heat-sensitive allele 83201 is especially useful for mutant enrichment (832, 1043). Used in the first experiments reporting transformation of Neurospora by N. crassaDNA (677, 679) and reported to be efficient as a recipient in absence of inositol (1162). Used to study glucose (917) and sulfate (641) transport systems. Used extensively for studying induced reversion (392). Used for studying the mechanism of inositol-less death (647, 702), mutagenicity of ferrous ions, and regulation of mitochondrial membrane fluidity; for a review, see reference 702. Spontaneous reversion rates (386). Allele-specific partial suppressor (390). Allele 46802 is nonrevertable and inseparable from translocation 46802 (386, 808). Strains carrying heat-sensitive allele 83201 show slow semicolonial growth in liquid minimal medium at 25°C (641), but look normal on slants (D.D. Perkins, unpublished data). Strains carrying allele 89601 contain cross-reacting material (1183). Mutant gene exo-1 is present in the inl(89601) a stock FGSC 498 and may, therefore, be present in stocks of mutants derived by inositol-less death. (See references 194, 325, and 1027). Called inos.	VR	B
mei-3	IL. Right of arg-1 (3%). Probably right of eth-1 (1%) and arg-3 (1%). Left of the T(39311)right breakpoint; hence, left of the centromere and sn (757, 808).Homozygous barren (757). Recessive. Blocks meiosis in zygotene (860). Sensitive to UV, histidine (757, 759), mitomycin C (195), ionizing radiation, and methyl methane sulfonate (939). Sensitivity to UV and histidine is temperature sensitive; best scored at 39 C, at least for strains carrying allele N289 (757). Causes increased duplication instability (mitotic recombination, deletion, or both) (757).	IL	B