Bailly Julie, Fraissinet-Tachet Laurence, Verner Marie-Christine, Debaud Jean-Claude, Lemaire Marc, Wésolowski-Louvel Micheline, Marmeisse Roland
Ecologie Microbienne, UMR CNRS, USC INRA, Université de Lyon, Université Lyon 1, Villeurbanne, France.
ISME J. 2007 Nov;1(7):632-42. doi: 10.1038/ismej.2007.68. Epub 2007 Sep 20.
To appreciate the functional diversity of communities of soil eukaryotic micro-organisms we evaluated an experimental approach based on the construction and screening of a cDNA library using polyadenylated mRNA extracted from a forest soil. Such a library contains genes that are expressed by each of the different organisms forming the community and represents its metatranscriptome. The diversity of the organisms that contributed to this library was evaluated by sequencing a portion of the 18S rDNA gene amplified from either soil DNA or reverse-transcribed RNA. More than 70% of the sequences were from fungi and unicellular eukaryotes (protists) while the other most represented group was the metazoa. Calculation of richness estimators suggested that more than 180 species could be present in the soil samples studied. Sequencing of 119 cDNA identified genes with no homologues in databases (32%) and genes coding proteins involved in different biochemical and cellular processes. Surprisingly, the taxonomic distribution of the cDNA and of the 18S rDNA genes did not coincide, with a marked under-representation of the protists among the cDNA. Specific genes from such an environmental cDNA library could be isolated by expression in a heterologous microbial host, Saccharomyces cerevisiae. This is illustrated by the functional complementation of a histidine auxotrophic yeast mutant by two cDNA originating possibly from an ascomycete and a basidiomycete fungal species. Study of the metatranscriptome has the potential to uncover adaptations of whole microbial communities to local environmental conditions. It also gives access to an abundant source of genes of biotechnological interest.
为了认识土壤真核微生物群落的功能多样性,我们评估了一种基于构建和筛选cDNA文库的实验方法,该文库使用从森林土壤中提取的聚腺苷酸化mRNA构建。这样的文库包含由构成群落的每种不同生物体表达的基因,并代表其元转录组。通过对从土壤DNA或逆转录RNA扩增的18S rDNA基因的一部分进行测序,评估了对该文库有贡献的生物体的多样性。超过70%的序列来自真菌和单细胞真核生物(原生生物),而另一个最具代表性的群体是后生动物。丰富度估计值的计算表明,在所研究的土壤样本中可能存在180多种物种。对119个cDNA的测序鉴定出数据库中没有同源物的基因(32%)以及编码参与不同生化和细胞过程的蛋白质的基因。令人惊讶的是,cDNA和18S rDNA基因的分类分布不一致,原生生物在cDNA中的代表性明显不足。可以通过在异源微生物宿主酿酒酵母中表达来分离来自这种环境cDNA文库的特定基因。这通过两个可能源自子囊菌和担子菌真菌物种的cDNA对组氨酸营养缺陷型酵母突变体的功能互补得到了说明。对元转录组的研究有可能揭示整个微生物群落对当地环境条件的适应性。它还提供了一个丰富的具有生物技术意义的基因来源。