Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, WI, United States.
Fungal Genet Biol. 2010 May;47(5):423-32. doi: 10.1016/j.fgb.2010.02.006. Epub 2010 Feb 26.
Subtelomeric secondary metabolite (SM) gene clusters are frequently surrounded by DNA repeats and transposon-like elements. The Aspergillus nidulans penicillin cluster, 30kb from the telomere of chromosome VI, is bordered by such elements. Deletions of penicillin telomere proximal and distal border regions resulted in decreased penicillin production. A 3.7kb distal region called PbIa, consisting of the putative transposable element DNA-2, was examined further where its replacement by a pyrG marker presented a similar phenotype as loss of the global SM regulator LaeA, resulting in a decrease in penicillin gene expression and product formation. In contrast, placement of the pyrG marker on either side of PbIa had no effect on penicillin synthesis. A requirement for PbIa in penicillin production was also apparent in a histone deacetylase mutant, DeltahdaA, enhanced for penicillin production. Trans-complementation of the PbIa element near and within the terrequinone A cluster on chromosome V did not restore penicillin biosynthesis or increase production of terrequinone A. Taken together, this data provides evidence for transposon involvement in SM cluster regulation.
端粒下次代谢产物(SM)基因簇通常被 DNA 重复序列和转座子样元件包围。青霉青霉素簇位于染色体 VI 的端粒 30kb 处,其边界就存在这些元件。青霉素端粒近端和远端边界区域的缺失导致青霉素产量下降。一个 3.7kb 的远端区域称为 PbIa,由假定的可移动元件 DNA-2 组成,进一步研究发现,用 pyrG 标记替代它与丧失全局 SM 调节因子 LaeA 表现出相似的表型,导致青霉素基因表达和产物形成减少。相比之下,pyrG 标记在 PbIa 两侧的放置对青霉素合成没有影响。在青霉素产量方面,PbIa 在组蛋白去乙酰化酶突变体 DeltahdaA 中也很明显,这种突变体增强了青霉素的产量。在染色体 V 上的 terrequinone A 簇附近和内部的 PbIa 元件的反式互补并没有恢复青霉素的生物合成或增加 terrequinone A 的产量。总的来说,这些数据为转座子参与 SM 簇调控提供了证据。