AI Article Synopsis

  • Mutants of Neurospora tetrasperma were studied for issues in polyol metabolism and protoperithecial development, showing that when certain polyols are used instead of sucrose, these mutants often fail to utilize multiple polyols.
  • These mutants were learned to complement each other at different development stages, notably resulting in mature protoperithecia and perithecia when combined with opposite mating types.
  • Two specific mutants that cannot utilize glycerol were analyzed genetically, revealing their mapping locations and links to different genes related to glycerol metabolism, with one mapping close to ad-1 and rib-1, while the other is near ad-9 in linkage group I.

Article Abstract

Mutants defective in polyol metabolism and/or in protoperithecial development were selected in Neurospora tetrasperma, a species in which protoperithecial development occurs at nonpermissively high temperature if certain polyols are used in lieu of sucrose as carbon source. Mutants selected for nonutilization of one of the four polyols tested, glycerol, mannitol, sorbitol, or xylitol, were usually found to be nonutilizers of the other three polyols as well. Mutants blocked at various stages of protoperithecial development complemented pairwise to produce more advanced developmental stages, usually mature protoperithecia and, when of opposite mating type, mature perithecia. About one-third of the mutants manifested both polyol auxotrophy and defective protoperithecial development upon initial isolation, but protoperithecial defectiveness in such mutants usually showed erratic segregation in crosses and/or instability to repeated vegetative transfer, whereas polyol auxotrophy usually did not and was, therefore, studied further. Two glycerol nonutilizing strains were introgressed into N. crassa to facilitate genetic analysis. One, glp-4, lacked both inducible and constitutive glycerol kinase and mapped to linkage group VI, between ad-1 and rib-1; the other, glp-5, lacked glyceraldehyde kinase and mapped to linkage group I, proximal to ad-9. Another mutant, gly-u(234), has been reported by other investigators to lack inducible glycerol kinase but to map to linkage group I, distal to ad-9.

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http://dx.doi.org/10.1007/BF01035993DOI Listing

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