Division of Biology, School of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR.
Fungal Genet Biol. 2011 Apr;48(4):359-69. doi: 10.1016/j.fgb.2011.01.009. Epub 2011 Jan 31.
This study investigated the molecular mechanism of the fruiting body development and sporulation in the cap of the Shiitake mushroom, Lentinula edodes. Although there has been much research into L. edodes, there remain significant gaps in our knowledge of how the species reproduces. In order to provide molecular resources and to understand the molecular mechanism of the fruiting body development in basidiomycete comprehensively, we searched for the genes which are important for fruiting body development and sporulation in the cap of mature fruiting body of L. edodes by using the whole-genome approach. Massive cDNA pyrosequencing was used to generate >7000 sequence contigs from mature fruiting bodies. We used Gene Ontology to categorize the contigs to form the catalog of genes expressed at the stage of the mature fruiting body. We also assigned the contigs into the KEGG pathways. The catalog of expressed genes indicates that the mature fruiting bodies (1) sense the external environment, (2) transmit signals to express genes through regulatory systems, (3) produce many proteins, (4) degrade unwanted proteins, (5) perform extensive biosynthesis, (6) generate energy, (7) regulate the internal environment, (8) transport molecules, (9) carry out cell division, and (10) differentiate and develop. After establishing the catalog of expressed genes in L. edodes, we used the LongSAGE approach to analyze the expression levels of genes found in mature fruiting bodies before (FB) and after (FBS) spores appeared. Gene-expression patterns according to GO categories were similar in these two stages. We have also successfully identified genes differentially expressed in FB and FBS. Fold-changes in expression levels of selected genes based on LongSAGE tag counts were similar to those obtained by real-time RT-PCR. The consistency between real-time RT-PCR and LongSAGE results indicates reliability of the LongSAGE results. Overall, this study provides valuable information on the fruiting processes of L. edodes through a combination of massive cDNA pyrosequencing and LongSAGE sequencing, and the knowledge thereby obtained may provide insight into the improvement of the yield of commercially grown Shiitake mushrooms.
本研究调查了香菇子实体发育和孢子形成的分子机制。虽然已经对香菇进行了大量研究,但我们对该物种的繁殖方式仍知之甚少。为了提供分子资源并全面了解担子菌子实体发育的分子机制,我们通过全基因组方法,在香菇成熟子实体的帽中搜索对其发育和孢子形成重要的基因。大规模 cDNA 焦磷酸测序用于从成熟子实体中生成>7000 个序列连续片段。我们使用基因本体论将连续片段分类,形成成熟子实体阶段表达的基因目录。我们还将连续片段分配到 KEGG 途径中。表达基因目录表明,成熟子实体 (1) 感知外部环境,(2) 通过调节系统将信号传递到表达基因,(3) 产生许多蛋白质,(4) 降解不需要的蛋白质,(5) 进行广泛的生物合成,(6) 产生能量,(7) 调节内部环境,(8) 转运分子,(9) 进行细胞分裂,以及 (10) 分化和发育。在建立香菇表达基因目录后,我们使用 LongSAGE 方法分析成熟子实体在孢子出现前后 (FB 和 FBS) 的基因表达水平。这两个阶段根据 GO 类别的基因表达模式相似。我们还成功地鉴定了 FB 和 FBS 中差异表达的基因。根据 LongSAGE 标签计数确定的选定基因表达水平的变化与实时 RT-PCR 获得的变化相似。基于实时 RT-PCR 和 LongSAGE 结果的一致性表明 LongSAGE 结果的可靠性。总的来说,这项研究通过大规模 cDNA 焦磷酸测序和 LongSAGE 测序的组合,为香菇的果实发育过程提供了有价值的信息,并且由此获得的知识可能为提高商业种植香菇的产量提供了深入的了解。