Department of Plant and Microbial Biology, California Institute for Quantitative Biosciences (QB3)/Chemistry Mass Spectrometry Facility, University of California, Berkeley, CA 94720, USA.
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22157-62. doi: 10.1073/pnas.0906810106. Epub 2009 Dec 15.
The filamentous fungus Neurospora crassa is a model laboratory organism, but in nature is commonly found growing on dead plant material, particularly grasses. Using functional genomics resources available for N. crassa, which include a near-full genome deletion strain set and whole genome microarrays, we undertook a system-wide analysis of plant cell wall and cellulose degradation. We identified approximately 770 genes that showed expression differences when N. crassa was cultured on ground Miscanthus stems as a sole carbon source. An overlap set of 114 genes was identified from expression analysis of N. crassa grown on pure cellulose. Functional annotation of up-regulated genes showed enrichment for proteins predicted to be involved in plant cell wall degradation, but also many genes encoding proteins of unknown function. As a complement to expression data, the secretome associated with N. crassa growth on Miscanthus and cellulose was determined using a shotgun proteomics approach. Over 50 proteins were identified, including 10 of the 23 predicted N. crassa cellulases. Strains containing deletions in genes encoding 16 proteins detected in both the microarray and mass spectrometry experiments were analyzed for phenotypic changes during growth on crystalline cellulose and for cellulase activity. While growth of some of the deletion strains on cellulose was severely diminished, other deletion strains produced higher levels of extracellular proteins that showed increased cellulase activity. These results show that the powerful tools available in N. crassa allow for a comprehensive system level understanding of plant cell wall degradation mechanisms used by a ubiquitous filamentous fungus.
丝状真菌粗糙脉孢菌是一种模式实验室生物,但在自然界中通常生长在死亡的植物材料上,特别是草上。利用粗糙脉孢菌现有的功能基因组学资源,包括一个近乎完整的基因组缺失株系集和全基因组微阵列,我们对植物细胞壁和纤维素降解进行了系统分析。当粗糙脉孢菌以地面芒草茎作为唯一碳源进行培养时,我们鉴定了大约 770 个表现出表达差异的基因。从纯纤维素上生长的粗糙脉孢菌的表达分析中,确定了一组 114 个重叠基因。上调基因的功能注释表明,与参与植物细胞壁降解的蛋白质预测有富集,但也有许多基因编码未知功能的蛋白质。作为表达数据的补充,使用鸟枪法蛋白质组学方法确定了与粗糙脉孢菌在芒草和纤维素上生长相关的分泌组。鉴定出 50 多种蛋白质,包括 23 个预测的粗糙脉孢菌纤维素酶中的 10 个。对在微阵列和质谱实验中都检测到的编码 16 种蛋白质的基因缺失株系进行分析,以研究其在结晶纤维素上生长时的表型变化和纤维素酶活性。虽然一些缺失株系在纤维素上的生长受到严重抑制,但其他缺失株系产生了更高水平的细胞外蛋白,显示出更高的纤维素酶活性。这些结果表明,粗糙脉孢菌现有的强大工具允许对一种普遍存在的丝状真菌用于植物细胞壁降解的机制进行全面的系统水平理解。