Horton J S, Palmer G E, Smith W J
Department of Biological Sciences, Union College, Schenectady, New York 12308,
Fungal Genet Biol. 1999 Feb;26(1):33-47. doi: 10.1006/fgbi.1998.1104.
The gene FRT1 has previously been shown to induce homokaryotic fruiting in transformation recipients of the basidiomycete Schizophyllum commune. In this paper, we demonstrate by gene disruption experiments that FRT1 is dispensable for dikaryotic fruiting. Nonfruiting homokaryotic FRT1 disruptant strains exhibited enhanced aerial growth of mycelia compared to wild type. Introduction of a functional FRT1 allele into the disruptant restored the wild-type colony morphology. Transcript abundance of the dikaryon-expressed SC1 and SC4 hydrophobin genes and the SC7 gene were greatly elevated in homokaryotic FRT1 disruptant strains. Growth of the disruptant strains under continuous light was found to inhibit the elevation of SC1 and SC4 transcript levels, but not of SC7 mRNA. These data suggest that the role of FRT1 in vegetatively growing homokaryons is to act as a negative regulator of dikaryon-expressed genes.
基因FRT1此前已被证明可在担子菌裂褶菌的转化受体中诱导单核结实。在本文中,我们通过基因敲除实验证明,FRT1对于双核结实并非必需。与野生型相比,不结实的单核FRT1敲除菌株表现出菌丝体气生生长增强。将功能性FRT1等位基因导入敲除菌株可恢复野生型菌落形态。在单核FRT1敲除菌株中,双核表达的疏水蛋白基因SC1和SC4以及SC7基因的转录丰度大幅升高。发现敲除菌株在持续光照下生长会抑制SC1和SC4转录水平的升高,但不会抑制SC7 mRNA的升高。这些数据表明,FRT1在营养生长的单核体中的作用是作为双核表达基因的负调节因子。