Saloheimo Markku, Valkonen Mari, Penttilä Merja
VTT Biotechnology, 02044 VTT, Finland.
Mol Microbiol. 2003 Feb;47(4):1149-61. doi: 10.1046/j.1365-2958.2003.03363.x.
The unfolded protein response (UPR) is a regulatory pathway activating genes involved in multiple functions related to folding, quality control and transport of secreted proteins. Characterization of the hac1/hacA genes encoding the UPR transcription factors from the filamentous fungi Trichoderma reesei and Aspergillus nidulans is described in this article. The corresponding gene in Saccharomyces cerevisiae is activated through a non-spliceosomal intron-splicing reaction. The T. reesei hac1 and A. nidulans hacA mRNAs undergo an analogous splicing reaction of a 20-nt-long intron during UPR induction. This splicing changes the reading frame of the mRNA and thus could bring in an activation domain to the HACI/HACA proteins. In addition to the non-spliceosomal splicing, the hac1/A mRNAs of the filamentous fungi are truncated at the 5'-flanking region upon UPR induction. An upstream open reading frame is omitted from the mRNAs due to the truncation, and evidence is presented showing that the truncated T. reesei hac1 mRNA is translated more efficiently than a full-length mRNA. This paper reports a novel combination of two different regulatory mechanisms of a transcription factor gene, both operational at the mRNA level.
未折叠蛋白反应(UPR)是一条激活与分泌蛋白折叠、质量控制和运输等多种功能相关基因的调控途径。本文描述了来自丝状真菌里氏木霉和构巢曲霉的编码UPR转录因子的hac1/hacA基因的特征。酿酒酵母中的相应基因通过非剪接体的内含子剪接反应被激活。在UPR诱导过程中,里氏木霉hac1和构巢曲霉hacA mRNA经历了一个20个核苷酸长的内含子的类似剪接反应。这种剪接改变了mRNA的阅读框,从而可能为HACI/HACA蛋白引入一个激活结构域。除了非剪接体剪接外,丝状真菌的hac1/A mRNA在UPR诱导时在5'侧翼区域被截断。由于截断,mRNA中一个上游开放阅读框被省略,并且有证据表明截短的里氏木霉hac1 mRNA比全长mRNA翻译效率更高。本文报道了转录因子基因的两种不同调控机制的一种新组合,这两种机制均在mRNA水平上起作用。