Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0002527
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dc.titleSimultaneous assessment of soil microbial community structure and function through analysis of the meta-transcriptome
dc.contributor.authorUrich T.
dc.contributor.authorLanz閚 A.
dc.contributor.authorQi J.
dc.contributor.authorHuson D.H.
dc.contributor.authorSchleper C.
dc.contributor.authorSchuster S.C.
dc.date.accessioned2019-11-08T00:56:02Z
dc.date.available2019-11-08T00:56:02Z
dc.date.issued2008
dc.identifier.citationUrich T., Lanz閚 A., Qi J., Huson D.H., Schleper C., Schuster S.C. (2008). Simultaneous assessment of soil microbial community structure and function through analysis of the meta-transcriptome. PLoS ONE 3 (6) : e2527. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0002527
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161852
dc.description.abstractBackground: Soil ecosystems harbor the most complex prokaryotic and eukaryotic microbial communities on Earth. Experimental approaches studying these systems usually focus on either the soil community's taxonomic structure or its functional characteristics. Many methods target DNA as marker molecule and use PCR for amplification. Methodology/Principal Findings: Here we apply an RNA-centered meta-transcriptomic approach to simultaneously obtain information on both structure and function of a soil community. Total community RNA is random reversely transcribed into cDNA without any PCR or cloning step. Direct pyrosequencing produces large numbers of cDNA rRNA-tags; these are taxonomically profiled in a binding approach using the MEGAN software and two specifically compiled rRNA reference databases containing small and large subunit rRNA sequences. The pyrosequencing also produces mRNA-tags; these provide a sequence-based transcriptome of the community. One soil dataset of 258,411 RNA-tags of ?98 bp length contained 193,219 rRNA-tags with valid taxonomic information, together with 21,133 mRNA-tags. Quantitative information about the relative abundance of organism from all three domains of life and from different trophic levels was obtained in a single experiment. Less frequent taxa, such as soil Crenarchaeota, were well represented in the data set. These were identified by more than 2,000 rRNA-tags; furthrmore, their activity in situ was revealed through the presence of mRNA-tags specific for enzymes involved in ammonia oxidation and CO2 fixation. Conclusions/Significance: This approach could be widely applied in microbial ecology by efficiently linking community structure and function in a single experiment while avoiding biases inherent in other methods. � 2008 Urich et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectammonia
dc.subjectcarbon dioxide
dc.subjectcomplementary DNA
dc.subjectmessenger RNA
dc.subjectribosome RNA
dc.subjectRNA
dc.subjectbacterial RNA
dc.subjectmessenger RNA
dc.subjectribosome RNA
dc.subjectarticle
dc.subjectbiodiversity
dc.subjectcarbon dioxide fixation
dc.subjectcommunity structure
dc.subjectcontrolled study
dc.subjectCrenarchaeota
dc.subjectgene expression profiling
dc.subjectgenome size
dc.subjectmicrobial community
dc.subjectnonhuman
dc.subjectnucleotide sequence
dc.subjectoxidation
dc.subjectpolymerase chain reaction
dc.subjectpyrosequencing
dc.subjectreverse transcription
dc.subjectRNA sequence
dc.subjectsequence alignment
dc.subjectsequence database
dc.subjectsoil microflora
dc.subjecttaxonomy
dc.subjecttranscriptomics
dc.subjectecosystem
dc.subjectgenetics
dc.subjectmicrobiology
dc.subjectspecies difference
dc.subjectCrenarchaeota
dc.subjectEukaryota
dc.subjectProkaryota
dc.subjectEcosystem
dc.subjectRNA, Bacterial
dc.subjectRNA, Messenger
dc.subjectRNA, Ribosomal
dc.subjectSoil Microbiology
dc.subjectSpecies Specificity
dc.typeArticle
dc.contributor.departmentLIFE SCIENCES INSTITUTE
dc.description.doi10.1371/journal.pone.0002527
dc.description.sourcetitlePLoS ONE
dc.description.volume3
dc.description.issue6
dc.description.pagee2527
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