Evidence map›Paper›PMID 25525151›Full record

ArticleRNA (New York, N.Y.)2015

Identification, expression, and molecular evolution of microRNAs in the "living fossil" Triops cancriformis (tadpole shrimp).

Kahori T Ikeda, Yuka Hirose, Kiriko Hiraoka, Emiko Noro, Kosuke Fujishima, Masaru Tomita, Akio Kanai

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 35 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Kahori T IkedaInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-0882, Japan.
Yuka HiroseInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-0882, Japan.
Kiriko HiraokaInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan.
Emiko NoroInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan.
Kosuke FujishimaInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan University Affiliated Research Center, NASA Ames Research Center, Moffett Field, California 94043, USA.
Masaru TomitaInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-0882, Japan Faculty of Environment and Information Studies, Keio University, Fujisawa 252-0882, Japan.
Akio KanaiInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-0882, Japan Faculty of Environment and Information Studies, Keio University, Fujisawa 252-0882, Japan akio@sfc.keio.ac.jp.
Keio University · JPAmes Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs have been identified and analyzed in various model species, but an investigation of miRNAs in nonmodel species is required for a more complete understanding of miRNA evolution. In this study, we investigated the miRNAs of the nonmodel species Triops cancriformis (tadpole shrimp), a "living fossil," whose morphological form has not changed in almost 200 million years. Dramatic ontogenetic changes occur during its development. To clarify the evolution of miRNAs, we comparatively analyzed its miRNAs and the components of its RNAi machinery. We used deep sequencing to analyze small RNA libraries from the six different developmental stages of T. cancriformis (egg, first-fourth instars, and adult), and also analyzed its genomic DNA with deep sequencing. We identified 180 miRNAs (87 conserved miRNAs and 93 novel candidate miRNAs), and deduced the components of its RNAi machinery: the DICER1, AGO1-3, PIWI, and AUB proteins. A comparative miRNA analysis of T. cancriformis and Drosophila melanogaster showed inconsistencies in the expression patterns of four conserved miRNAs. This suggests that although the miRNA sequences of the two species are very similar, their roles differ across the species. An miRNA conservation analysis revealed that most of the conserved T. cancriformis miRNAs share sequence similarities with those of arthropods, although T. cancriformis is called a "living fossil." However, we found that let-7 and DICER1 of T. cancriformis are more similar to those of the vertebrates than to those of the arthropods. These results suggest that miRNA systems of T. cancriformis have evolved in a unique fashion.

Indexed as

TranscriptomeAnimalsArgonaute ProteinsBase SequenceConserved SequenceCrustaceaEvolution, MolecularMicroRNAsMolecular Sequence AnnotationMultigene FamilyPhylogenyRibonuclease IIIArgonaute ProteinsMicroRNAsRibonuclease IIIdeep sequencingdevelopmentevolutionmicroRNAT. cancriformis

Identifiers

PMID25525151
PMCPMC4338350
OpenAlexW2161243071

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.