Roy Preeti, Lockington Robin A, Kelly Joan M
School of Molecular and Biomedical Science, University of Adelaide, Adelaide 5005, Australia.
Fungal Genet Biol. 2008 May;45(5):657-70. doi: 10.1016/j.fgb.2007.10.016. Epub 2007 Nov 1.
The major regulatory protein in carbon repression in Aspergillus nidulans is CreA. Strains constitutively over-expressing creA show normal responses to carbon repression, indicating that auto-regulation of creA is not essential for CreA-mediated regulation. In these strains, high levels of CreA are present whether cells are grown in repressing or derepressing conditions, indicating large-scale degradation of CreA does not play a key role. CreA is located in the nucleus and cytoplasm in cells when grown in either repressing or derepressing conditions, and absence of CreB, CreD or AcrB does not affect either the localisation or amount of CreA. Therefore, CreA must require some modification or interaction to act as a repressor. Deletion analysis indicates that a region of CreA thought to be important for repression in Trichoderma reesei and Sclerotina sclerotiorum CreA homologues is not critical for function in Aspergillus nidulans.
构巢曲霉中碳代谢阻遏的主要调节蛋白是CreA。组成型过表达creA的菌株对碳代谢阻遏表现出正常反应,这表明creA的自我调节对于CreA介导的调节并非必不可少。在这些菌株中,无论细胞是在阻遏条件还是去阻遏条件下生长,都存在高水平的CreA,这表明CreA的大规模降解并不起关键作用。当在阻遏或去阻遏条件下生长时,CreA位于细胞的细胞核和细胞质中,并且缺失CreB、CreD或AcrB并不影响CreA的定位或数量。因此,CreA必须进行一些修饰或相互作用才能作为阻遏物发挥作用。缺失分析表明,被认为对里氏木霉和核盘菌CreA同源物中的阻遏很重要的CreA区域,对构巢曲霉中的功能并不关键。