4.5 Article

Solution Hybrid Selection Capture for the Recovery of Functional Full-Length Eukaryotic cDNAs From Complex Environmental Samples

Journal

DNA RESEARCH
Volume 21, Issue 6, Pages 685-694

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/dnares/dsu030

Keywords

metatranscriptomics; soil RNA; soil eukaryotes; sequence capture; glycoside hydrolase family GH11

Funding

  1. University of Turin
  2. region Rhone-Alpes (CMIRA program)
  3. Ministere de l'Enseignement Superieur et de la Recherche
  4. Direction Generale de l'Armement
  5. Agence Nationale pour la Recherche
  6. CNRS-INSU ECCO Microbien program
  7. INRA metaprogramme M2E (project Metascreen)
  8. EU-project 'EcoFINDERS' [264465]
  9. Centre national de la recherche scientifique (CNRS)
  10. [ANR 09-GENM-033-001]

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Eukaryotic microbial communities play key functional roles in soil biology and potentially represent a rich source of natural products including biocatalysts. Culture-independent molecular methods are powerful tools to isolate functional genes from uncultured microorganisms. However, none of the methods used in environmental genomics allow for a rapid isolation of numerous functional genes from eukaryotic microbial communities. We developed an original adaptation of the solution hybrid selection (SHS) for an efficient recovery of functional complementary DNAs (cDNAs) synthesized from soil-extracted polyadenylated mRNAs. This protocol was tested on the Glycoside Hydrolase 11 gene family encoding endo-xylanases for which we designed 35 explorative 31-mers capture probes. SHS was implemented on four soil eukaryotic cDNA pools. After two successive rounds of capture, >90% of the resulting cDNAs were GH11 sequences, of which 70% (38 among 53 sequenced genes) were full length. Between 1.5 and 25% of the cloned captured sequences were expressed in Saccharomyces cerevisiae. Sequencing of polymerase chain reaction-amplified GH11 gene fragments from the captured sequences highlighted hundreds of phylogenetically diverse sequences that were not yet described, in public databases. This protocol offers the possibility of performing exhaustive exploration of eukaryotic gene families within microbial communities thriving in any type of environment.

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