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利用快速消减杂交方法克隆在嗜热栖热放线菌纤维素酶诱导早期表达的基因。

Cloning of genes expressed early during cellulase induction in Hypocrea jecorina by a rapid subtraction hybridization approach.

作者信息

Schmoll Monika, Zeilinger Susanne, Mach Robert L, Kubicek Christian P

机构信息

Division of Gene Technology and Applied Biochemistry, Institute for Chemical Engineering, Vienna University of Technology, Getreidemarkt 9/1665, A-1060 Wien, Austria.

出版信息

Fungal Genet Biol. 2004 Sep;41(9):877-87. doi: 10.1016/j.fgb.2004.06.002.

Abstract

The cellulase system of the filamentous fungus Hypocrea jecorina (Trichoderma reesei) is encoded by several cellobiohydrolase, endoglucanase and beta-glucosidase genes, which are co-ordinately expressed upon induction by cellulose or the disaccharide sophorose. To identify genes, which are specifically expressed under these inducing conditions and possibly related to the induction process, we applied rapid subtraction hybridization (RaSH) to sophorose induced mRNAs from the wild-type strain H. jecorina QM9414 and a mutant strain H. jecorina QM9978, which is defective in the induction of cellulase gene expression. From a total of 224 clones, 22 gene fragments representing 20 different genes were analyzed. These included one gene encoding a PAS-domain protein with similarity to the Neurospora clock modulator VIVID; one gene similar to Podospora anserina ami1 involved in nuclear migration and the genes encoding translation elongation factor 1alpha, the transcriptional activator Hap5, and myo-inositol-1-phosphate synthase; in addition, several genes were detected, whose function is unknown. Some of them did not even have potential homologues in the Neurospora or Fusarium genome databases. The differential regulation of expression of those 20 genes by sophorose in wild-type and mutant was verified by Northern blotting. Their consistent response to additional inducing conditions (cellulose) confirms their interconnection with cellulase formation.

摘要

丝状真菌里氏木霉(哈茨木霉)的纤维素酶系统由几个纤维二糖水解酶、内切葡聚糖酶和β-葡萄糖苷酶基因编码,这些基因在纤维素或二糖槐糖诱导下协同表达。为了鉴定在这些诱导条件下特异性表达且可能与诱导过程相关的基因,我们对野生型菌株里氏木霉QM9414和纤维素酶基因表达诱导存在缺陷的突变株里氏木霉QM9978经槐糖诱导的mRNA应用了快速消减杂交(RaSH)技术。从总共224个克隆中,分析了代表20个不同基因的22个基因片段。这些基因包括一个编码与粗糙脉孢菌生物钟调节因子VIVID相似的含PAS结构域蛋白的基因;一个与参与核迁移的嗜热栖热放线菌ami1相似的基因,以及编码翻译延伸因子1α、转录激活因子Hap5和肌醇-1-磷酸合酶的基因;此外,还检测到几个功能未知的基因。其中一些基因在粗糙脉孢菌或镰刀菌基因组数据库中甚至没有潜在的同源物。通过Northern印迹法验证了这20个基因在野生型和突变体中受槐糖的差异表达调控。它们对其他诱导条件(纤维素)的一致反应证实了它们与纤维素酶形成的相互联系。

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