Katz M E, Masoumi A, Burrows S R, Shirtliff C G, Cheetham B F
Molecular and Cellular Biology Division, School of Biological Sciences, University of New England, Armidale, New South Wales 2351, Australia.
Genetics. 2000 Dec;156(4):1559-71. doi: 10.1093/genetics/156.4.1559.
The extracellular proteases of Aspergillus nidulans are produced in response to limitation of carbon, nitrogen, or sulfur, even in the absence of exogenous protein. Mutations in the A. nidulans xprF and xprG genes have been shown to result in elevated levels of extracellular protease in response to carbon limitation. The xprF gene was isolated and sequence analysis indicates that it encodes a 615-amino-acid protein, which represents a new type of fungal hexokinase or hexokinase-like protein. In addition to their catalytic role, hexokinases are thought to be involved in triggering carbon catabolite repression. Sequence analysis of the xprF1 and xprF2 alleles showed that both alleles contain nonsense mutations. No loss of glucose or fructose phosphorylating activity was detected in xprF1 or xprF2 mutants. There are two possible explanations for this observation: (1) the xprF gene may encode a minor hexokinase or (2) the xprF gene may encode a protein with no hexose phosphorylating activity. Genetic evidence suggests that the xprF and xprG genes are involved in the same regulatory pathway. Support for this hypothesis was provided by the identification of a new class of xprG(-) mutation that suppresses the xprF1 mutation and results in a protease-deficient phenotype.
构巢曲霉的细胞外蛋白酶是在碳、氮或硫受限的情况下产生的,即使没有外源蛋白质也是如此。已证明构巢曲霉xprF和xprG基因的突变会导致在碳限制条件下细胞外蛋白酶水平升高。xprF基因已被分离,序列分析表明它编码一种615个氨基酸的蛋白质,这代表了一种新型的真菌己糖激酶或己糖激酶样蛋白质。除了其催化作用外,己糖激酶还被认为参与触发碳分解代谢物阻遏。xprF1和xprF2等位基因的序列分析表明,这两个等位基因都含有无义突变。在xprF1或xprF2突变体中未检测到葡萄糖或果糖磷酸化活性的丧失。对于这一观察结果有两种可能的解释:(1)xprF基因可能编码一种次要的己糖激酶;(2)xprF基因可能编码一种没有己糖磷酸化活性的蛋白质。遗传证据表明,xprF和xprG基因参与相同的调控途径。对这一假设的支持来自于鉴定出一类新的xprG(-)突变,该突变抑制xprF1突变并导致蛋白酶缺陷表型。