Guillemette Thomas, van Peij Noël N M E, Goosen Theo, Lanthaler Karin, Robson Geoffrey D, van den Hondel Cees A M J J, Stam Hein, Archer David B
School of Biology, University of Nottingham, University Park, Nottingham, UK.
BMC Genomics. 2007 Jun 11;8:158. doi: 10.1186/1471-2164-8-158.
Filamentous fungi such as Aspergillus niger have a high capacity secretory system and are therefore widely exploited for the industrial production of native and heterologous proteins. However, in most cases the yields of non-fungal proteins are significantly lower than those obtained for fungal proteins. One well-studied bottleneck appears to be the result of mis-folding of heterologous proteins in the ER during early stages of secretion, with related stress responses in the host, including the unfolded protein response (UPR). This study aims at uncovering transcriptional and translational responses occurring in A. niger exposed to secretion stress.
A genome-wide transcriptional analysis of protein secretion-related stress responses was determined using Affymetrix DNA GeneChips and independent verification for selected genes. Endoplasmic reticulum (ER)-associated stress was induced either by chemical treatment of the wild-type cells with dithiothreitol (DTT) or tunicamycin, or by expressing a human protein, tissue plasminogen activator (t-PA). All of these treatments triggered the UPR, as shown by the expression levels of several well-known UPR target genes. The predicted proteins encoded by most of the up-regulated genes function as part of the secretory system including chaperones, foldases, glycosylation enzymes, vesicle transport proteins, and ER-associated degradation proteins. Several genes were down-regulated under stress conditions and these included several genes that encode secreted enzymes. Moreover, translational regulation under ER stress was investigated by polysomal fractionation. This analysis confirmed the post-transcriptional control of hacA expression and highlighted that differential translation also occurs during ER stress, in particular for some genes encoding secreted proteins or proteins involved in ribosomal biogenesis and assembly.
This is first genome-wide analysis of both transcriptional and translational events following protein secretion stress. Insight has been gained into the molecular basis of protein secretion and secretion-related stress in an effective protein-secreting fungus, and provides an opportunity to identify target genes for manipulation in strain improvement strategies.
丝状真菌如黑曲霉具有高效的分泌系统,因此被广泛用于天然和异源蛋白质的工业生产。然而,在大多数情况下,非真菌蛋白质的产量显著低于真菌蛋白质。一个经过充分研究的瓶颈似乎是分泌早期异源蛋白质在内质网中错误折叠的结果,以及宿主中的相关应激反应,包括未折叠蛋白反应(UPR)。本研究旨在揭示黑曲霉在暴露于分泌应激时发生的转录和翻译反应。
使用Affymetrix DNA基因芯片确定了与蛋白质分泌相关应激反应的全基因组转录分析,并对选定基因进行了独立验证。通过用二硫苏糖醇(DTT)或衣霉素对野生型细胞进行化学处理,或通过表达人蛋白质组织纤溶酶原激活剂(t-PA)来诱导内质网(ER)相关应激。所有这些处理都触发了UPR,如几个著名的UPR靶基因的表达水平所示。大多数上调基因编码的预测蛋白质作为分泌系统的一部分发挥作用,包括伴侣蛋白、折叠酶、糖基化酶、囊泡运输蛋白和内质网相关降解蛋白。在应激条件下,有几个基因被下调,其中包括几个编码分泌酶的基因。此外,通过多核糖体分级分离研究了内质网应激下的翻译调控。该分析证实了hacA表达的转录后控制,并强调在内质网应激期间也会发生差异翻译,特别是对于一些编码分泌蛋白或参与核糖体生物合成和组装的蛋白质的基因。
这是首次对蛋白质分泌应激后的转录和翻译事件进行全基因组分析。我们深入了解了一种高效蛋白质分泌真菌中蛋白质分泌和分泌相关应激的分子基础,并为在菌株改良策略中鉴定可操作的靶基因提供了机会。