Evidence map›Paper›PMID 26554708›Full record

ArticlePloS one2015

High-Throughput Profiling of Caenorhabditis elegans Starvation-Responsive microRNAs.

Laura Garcia-Segura, Cei Abreu-Goodger, Armando Hernandez-Mendoza, Tzvetanka D Dimitrova Dinkova, Luis Padilla-Noriega, Martha Elva Perez-Andrade, Juan Miranda-Rios

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 23 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 4 institutions in 1 country.

Laura Garcia-SeguraPrograma de Doctorado en Ciencias Biomédicas, Universidad Nacional Autónoma de México (UNAM), México, D.F., México.
Cei Abreu-GoodgerUnidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, Guanajuato, México.
Armando Hernandez-MendozaCentro de Investigación en Dinámica Celular, Universidad Autónoma del Edo. de Morelos, Cuernavaca, Morelos, México.
Tzvetanka D Dimitrova DinkovaDepartamento de Bioquímica, Facultad de Química, Universidad Nacional Autónoma de México, México, D.F., México.
Luis Padilla-NoriegaDepartamento de Virología, Facultad de Medicina, Universidad Nacional Autónoma de México, México, D.F., México.
Martha Elva Perez-AndradeUnidad de Genética de la Nutrición, Depto. de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, UNAM e Instituto Nacional de Pediatría, México, D.F., México.
Juan Miranda-RiosUnidad de Genética de la Nutrición, Depto. de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, UNAM e Instituto Nacional de Pediatría, México, D.F., México.
Universidad Nacional Autónoma de México · MXInstituto Nacional de Pediatria · MXCenter for Research and Advanced Studies of the National Polytechnic Institute · MXUniversidad Autónoma del Estado de Morelos · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are non-coding RNAs of ~22 nucleotides in length that regulate gene expression by interfering with the stability and translation of mRNAs. Their expression is regulated during development, under a wide variety of stress conditions and in several pathological processes. In nature, animals often face feast or famine conditions. We observed that subjecting early L4 larvae from Caenorhabditis elegans to a 12-hr starvation period produced worms that are thinner and shorter than well-fed animals, with a decreased lipid accumulation, diminished progeny, reduced gonad size, and an increased lifespan. Our objective was to identify which of the 302 known miRNAs of C. elegans changed their expression under starvation conditions as compared to well-fed worms by means of deep sequencing in early L4 larvae. Our results indicate that 13 miRNAs (miR-34-3p, the family of miR-35-3p to miR-41-3p, miR-39-5p, miR-41-5p, miR-240-5p, miR-246-3p and miR-4813-5p) were upregulated, while 2 miRNAs (let-7-3p and miR-85-5p) were downregulated in 12-hr starved vs. well-fed early L4 larvae. Some of the predicted targets of the miRNAs that changed their expression in starvation conditions are involved in metabolic or developmental process. In particular, miRNAs of the miR-35 family were upregulated 6-20 fold upon starvation. Additionally, we showed that the expression of gld-1, important in oogenesis, a validated target of miR-35-3p, was downregulated when the expression of miR-35-3p was upregulated. The expression of another reported target, the cell cycle regulator lin-23, was unchanged during starvation. This study represents a starting point for a more comprehensive understanding of the role of miRNAs during starvation in C. elegans.

Indexed as

Gene ExpressionMicroRNAsAnimalsCaenorhabditis elegansGene Expression ProfilingHigh-Throughput Nucleotide SequencingSignal TransductionStarvationMicroRNAs

Identifiers

PMID26554708
PMCPMC4640506
OpenAlexW2243347490

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.