Bos C J, Debets A J, Swart K, Huybers A, Kobus G, Slakhorst S M
Department of Genetics, Agricultural University, Wageningen, The Netherlands.
Curr Genet. 1988 Nov;14(5):437-43. doi: 10.1007/BF00521266.
A start has been made on establishing a collection of Aspergillus niger colour and auxotrophic mutants with an isogenic background for use as a source of genetic markers. All strains have short conidiophores (csp A1), which makes them easy to handle on test plates. Genetic markers were combined stepwise by somatic recombination. Somatic diploids were obtained at frequencies of 10(-6) -10(-5) with conidiospores collected from a heterokaryon. The haploidization of heterozygous diploids was induced by benomyl. For unlinked markers, the frequency of recombinants varied from 35%-65%. Low frequencies of recombinants were found between markers on a same chromosome, but this was sometimes disturbed by mitotic crossing-over during an early stage of the diploid. Master strains were constructed having markers for six linkage groups.
已经开始建立一组具有同基因背景的黑曲霉颜色和营养缺陷型突变体,用作遗传标记的来源。所有菌株都有短分生孢子梗(csp A1),这使得它们在试验平板上易于处理。通过体细胞重组逐步组合遗传标记。从异核体收集的分生孢子以10^(-6)-10^(-5)的频率获得体细胞二倍体。用苯菌灵诱导杂合二倍体的单倍体化。对于不连锁的标记,重组体的频率在35%-65%之间变化。在同一染色体上的标记之间发现重组体的频率较低,但这有时会在二倍体早期被有丝分裂交换干扰。构建了具有六个连锁群标记的主菌株。