Sophianopoulou V, Suárez T, Diallinas G, Scazzocchio C
Institut de Génétique et Microbiologie, Unité Associée au CNRS 1354, Université Paris-Sud, Centre d'Orsay, France.
Mol Gen Genet. 1993 Jan;236(2-3):209-13. doi: 10.1007/BF00277114.
The proline utilisation gene cluster of Aspergillus nidulans can be repressed efficiently only when both repressing nitrogen and repressing carbon sources are present. We show that two cis-acting mutations in this cluster permit the efficient transcription of the prnB gene under repressing conditions, resulting in direct or indirect derepression of two other transcripts of the pathway. These mutations are transitions that define a 5'GAGACCCC3' sequence. Similar sequences are found upstream of other genes subject to carbon catabolite repression. We propose that this sequence defines the binding site for the negatively-acting CreA protein, which mediates carbon catabolite repression in this fungus.
只有当存在阻遏性氮源和阻遏性碳源时,构巢曲霉的脯氨酸利用基因簇才能被有效阻遏。我们发现,该基因簇中的两个顺式作用突变可使prnB基因在阻遏条件下高效转录,导致该途径的另外两个转录本直接或间接去阻遏。这些突变是转换,定义了一个5'GAGACCCC3'序列。在其他受碳分解代谢物阻遏的基因上游也发现了类似序列。我们提出,该序列定义了负向作用的CreA蛋白的结合位点,该蛋白介导了这种真菌中的碳分解代谢物阻遏。