Schmoll Monika, Dattenböck Christoph, Carreras-Villaseñor Nohemí, Mendoza-Mendoza Artemio, Tisch Doris, Alemán Mario Ivan, Baker Scott E, Brown Christopher, Cervantes-Badillo Mayte Guadalupe, Cetz-Chel José, Cristobal-Mondragon Gema Rosa, Delaye Luis, Esquivel-Naranjo Edgardo Ulises, Frischmann Alexa, Gallardo-Negrete Jose de Jesus, García-Esquivel Monica, Gomez-Rodriguez Elida Yazmin, Greenwood David R, Hernández-Oñate Miguel, Kruszewska Joanna S, Lawry Robert, Mora-Montes Hector M, Muñoz-Centeno Tania, Nieto-Jacobo Maria Fernanda, Nogueira Lopez Guillermo, Olmedo-Monfil Vianey, Osorio-Concepcion Macario, Piłsyk Sebastian, Pomraning Kyle R, Rodriguez-Iglesias Aroa, Rosales-Saavedra Maria Teresa, Sánchez-Arreguín J Alejandro, Seidl-Seiboth Verena, Stewart Alison, Uresti-Rivera Edith Elena, Wang Chih-Li, Wang Ting-Fang, Zeilinger Susanne, Casas-Flores Sergio, Herrera-Estrella Alfredo
Austrian Institute of Technology, Department Health and Environment, Bioresources Unit, Tulln, Austria
Austrian Institute of Technology, Department Health and Environment, Bioresources Unit, Tulln, Austria.
Microbiol Mol Biol Rev. 2016 Feb 10;80(1):205-327. doi: 10.1128/MMBR.00040-15. Print 2016 Mar.
The genus Trichoderma contains fungi with high relevance for humans, with applications in enzyme production for plant cell wall degradation and use in biocontrol. Here, we provide a broad, comprehensive overview of the genomic content of these species for "hot topic" research aspects, including CAZymes, transport, transcription factors, and development, along with a detailed analysis and annotation of less-studied topics, such as signal transduction, genome integrity, chromatin, photobiology, or lipid, sulfur, and nitrogen metabolism in T. reesei, T. atroviride, and T. virens, and we open up new perspectives to those topics discussed previously. In total, we covered more than 2,000 of the predicted 9,000 to 11,000 genes of each Trichoderma species discussed, which is >20% of the respective gene content. Additionally, we considered available transcriptome data for the annotated genes. Highlights of our analyses include overall carbohydrate cleavage preferences due to the different genomic contents and regulation of the respective genes. We found light regulation of many sulfur metabolic genes. Additionally, a new Golgi 1,2-mannosidase likely involved in N-linked glycosylation was detected, as were indications for the ability of Trichoderma spp. to generate hybrid galactose-containing N-linked glycans. The genomic inventory of effector proteins revealed numerous compounds unique to Trichoderma, and these warrant further investigation. We found interesting expansions in the Trichoderma genus in several signaling pathways, such as G-protein-coupled receptors, RAS GTPases, and casein kinases. A particularly interesting feature absolutely unique to T. atroviride is the duplication of the alternative sulfur amino acid synthesis pathway.
木霉属包含对人类具有高度相关性的真菌,可应用于生产用于降解植物细胞壁的酶以及生物防治。在此,我们针对“热门话题”研究方面,包括碳水化合物活性酶(CAZymes)、转运、转录因子和发育等,对这些物种的基因组内容进行了广泛而全面的概述,同时对里氏木霉、绿色木霉和哈茨木霉中信号转导、基因组完整性、染色质、光生物学或脂质、硫和氮代谢等研究较少的主题进行了详细分析和注释,并为之前讨论的那些主题开辟了新视角。我们总共涵盖了所讨论的每个木霉属物种预测的9000至11000个基因中的2000多个,这超过了各自基因含量的20%。此外,我们还考虑了已注释基因的可用转录组数据。我们分析的亮点包括由于不同的基因组内容和各自基因的调控而产生的总体碳水化合物裂解偏好。我们发现许多硫代谢基因受到光调节。此外,还检测到一种可能参与N - 连接糖基化的新型高尔基体1,2 - 甘露糖苷酶,同时也有迹象表明木霉属物种具有产生含半乳糖的杂合N - 连接聚糖的能力。效应蛋白的基因组清单揭示了许多木霉属特有的化合物,这些值得进一步研究。我们发现木霉属在几个信号通路中有趣地扩展,如G蛋白偶联受体、RAS GTP酶和酪蛋白激酶。绿色木霉绝对独特的一个特别有趣的特征是替代硫氨基酸合成途径的重复。