2013
DOI: 10.1016/j.dsr2.2012.08.008
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Identifying active foraminifera in the Sea of Japan using metatranscriptomic approach

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Cited by 39 publications
(33 citation statements)
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“…Previous studies reported overall similar communities of coastal marine protists recovered from DNA and RNA templates, with some revealing exceptions in particular groups (Logares et al, 2014; Massana et al, 2015; Lejzerowicz, Volstky & Pawlowski, 2013). Our results showed that eDNA and eRNA capture different community composition, affording useful information in particular for groups showing discordances for both templates.…”
Section: Discussionmentioning
confidence: 81%
“…Previous studies reported overall similar communities of coastal marine protists recovered from DNA and RNA templates, with some revealing exceptions in particular groups (Logares et al, 2014; Massana et al, 2015; Lejzerowicz, Volstky & Pawlowski, 2013). Our results showed that eDNA and eRNA capture different community composition, affording useful information in particular for groups showing discordances for both templates.…”
Section: Discussionmentioning
confidence: 81%
“…However, we cannot exclude that some of these sequences originated from the extracellular DNA known to be extremely abundant in deep-sea sediments (Dell'Anno and Danovaro, 2005). It is only by targeting RNA instead of DNA that their living state could be confirmed (Lejzerowicz et al, 2013b). Using RNA-based sequencing, surprisingly similar microbial communities were found active in the sediments of the investigated stations, exposed to contrasting levels of particulate organic matter (Ruff et al, 2014), suggesting comparable particulate organic matter qualities.…”
Section: Replicate Heterogeneity and Common Sequencesmentioning
confidence: 90%
“…Additional PCR amplifications were conducted using primer sets targeting foraminiferal SSU rDNA fragments of approximately 400 and approximately 1000 bp (see the electronic supplementary material, table S2). Sanger sequences were assigned as previously (foraminiferans, [8]; radiolarians, [9]) and clustered into operational taxonomic units (OTUs) as in Lejzerowicz et al [8] at 3 per cent divergence. Illumina sequences were treated separately and clustered to Sanger OTUs at 5 per cent divergence.…”
Section: Methodsmentioning
confidence: 99%
“…Controlled PCR amplifications realized in dedicated hoods (blank ratio 1 : 2 to 1 : 3) and using specific primers targeting the small subunit of the ribosomal RNA gene (SSU rDNA) of radiolarians (approx. 270 bp) or foraminiferans (68-196 bp) were prepared, cloned and Sanger sequenced as in Lejzerowicz et al [8] or using the next-generation sequencing (NGS) technology Illumina (MiSeq instrument). Additional PCR amplifications were conducted using primer sets targeting foraminiferal SSU rDNA fragments of approximately 400 and approximately 1000 bp (see the electronic supplementary material, table S2).…”
Section: Methodsmentioning
confidence: 99%