Vautard G, Cotton P, Fèvre M
Laboratoire de Biologie Cellulaire Fongique, UMR CNRS 5577, INSA, Université Lyon I, Villeurbanne, France.
FEBS Lett. 1999 Jun 18;453(1-2):54-8. doi: 10.1016/s0014-5793(99)00691-2.
We isolated the putative glucose repressor gene cre1 from the phytopathogenic fungus Sclerotinia sclerotiorum. cre1 encodes a 429 amino acid protein 59% similar to the carbon catabolite repressor CREA from Aspergillus nidulans. In addition to the overall amino acid sequence relatedness between CRE1 and CREA proteins, cre1 can functionally complement the A. nidulans creAd30 mutation as assessed by repression of the alcohol dehydrogenase I gene expression. The CREI region carrying the two zinc fingers is also very similar to the DNA binding domains of the Saccharomyces cerevisiae glucose repressors Mig1p and Mig2p. Despite the presence in the CRE1 protein of several motifs involved in the regulation of Miglp activity, cre1 cannot complement mig deficiencies in S. cerevisiae. These data suggest that glucose repression pathways may have evolved differently in yeasts and filamentous fungi.
我们从植物致病真菌核盘菌中分离出假定的葡萄糖阻遏基因cre1。cre1编码一种429个氨基酸的蛋白质,与构巢曲霉的碳分解代谢物阻遏蛋白CREA有59%的相似性。除了CRE1和CREA蛋白之间的整体氨基酸序列相关性外,通过对乙醇脱氢酶I基因表达的抑制评估,cre1能够在功能上互补构巢曲霉creAd30突变。携带两个锌指的CREI区域也与酿酒酵母葡萄糖阻遏蛋白Mig1p和Mig2p的DNA结合域非常相似。尽管CRE1蛋白中存在几个参与Mig1p活性调节的基序,但cre1不能互补酿酒酵母中的mig缺陷。这些数据表明,葡萄糖阻遏途径在酵母和丝状真菌中可能有不同的进化。