Swart K, van Heemst D, Slakhorst M, Debets F, Heyting C
Genetics and Molecular Genetics Groups, Wageningen University, Wageningen, 6703 HA, The Netherlands.
Fungal Genet Biol. 2001 Jun;33(1):25-35. doi: 10.1006/fgbi.2001.1266.
For the genetic dissection of sexual sporulation in Aspergillus nidulans, we started a collection of ascosporeless mutants. After mutagenization of conidiospores with high doses of UV, we isolated 20 mutants with defects in ascospore formation. We crossed these mutants in two successive rounds with the wild-type strain. Eighteen of the 20 isolated mutants produced progeny with the original mutant phenotype in these crosses, and these mutants were further analyzed. All 18 analyzed mutations were recessive to wild type. We assigned them to 15 complementation groups, based on crosses between mutants. The mutants could be classified as follows according to their cytological phenotype: (1) no croziers, (2) arrest at prekaryogamy, (3) arrest in early meiotic prophase, (4) arrest in late meiotic prophase, (5) arrest in meiotic metaphase I, (6) defective postmeiotic mitosis and/or deliniation of ascospores, and (7) slow progression through the postmeiotic stages of ascospore formation. A large proportion of the mutants, namely 11 of 18, arrested in meiotic prophase or metaphase I. We discuss a possible approach for isolating the wild-type alleles of the genes that carry the sexual sporulation mutations.
为了对构巢曲霉有性孢子形成进行遗传剖析,我们开始收集无囊孢子突变体。在用高剂量紫外线诱变分生孢子后,我们分离出了20个在囊孢子形成方面存在缺陷的突变体。我们将这些突变体与野生型菌株连续进行了两轮杂交。在这些杂交中,20个分离出的突变体中有18个产生了具有原始突变表型的后代,并对这些突变体进行了进一步分析。所有18个分析的突变相对于野生型都是隐性的。根据突变体之间的杂交,我们将它们归为15个互补群。根据它们的细胞学表型,这些突变体可分类如下:(1)无钩状体,(2)在核配前停滞,(3)在减数分裂前期早期停滞,(4)在减数分裂前期后期停滞,(5)在减数分裂中期I停滞,(6)减数分裂后有丝分裂和/或囊孢子轮廓形成缺陷,以及(7)在囊孢子形成的减数分裂后阶段进展缓慢。很大一部分突变体,即18个中的11个,在减数分裂前期或中期I停滞。我们讨论了一种分离携带性孢子形成突变的基因的野生型等位基因的可能方法。