Evidence map›Paper›PMID 26573611›Full record

ArticleMarine biotechnology (New York, N.Y.)2016

Silencing of Gonad-Inhibiting Hormone Transcripts in Litopenaeus vannamei Females by use of the RNA Interference Technology.

Rubens G Feijó, André L Braga, Carlos F C Lanes, Márcio A Figueiredo, Luis A Romano, Marta C Klosterhoff, Luis E M Nery, Rodrigo Maggioni, Wilson Wasielesky, Luis F Marins

Abstract read
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In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

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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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Transcriptional Regulation ofFrontiers in endocrinology · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
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

10 authors.

Rubens G FeijóMolecular Biology Laboratory, Biological Sciences Institute (ICB), Federal University of Rio Grande-FURG, Rio Grande, RS, 96203-900, Brazil.
André L BragaMarine Station of Aquaculture, Oceanography Institute, Federal University of Rio Grande, Rio Grande, RS, 96 201-900, Brazil.
Carlos F C LanesMolecular Biology Laboratory, Biological Sciences Institute (ICB), Federal University of Rio Grande-FURG, Rio Grande, RS, 96203-900, Brazil.
Márcio A FigueiredoMolecular Biology Laboratory, Biological Sciences Institute (ICB), Federal University of Rio Grande-FURG, Rio Grande, RS, 96203-900, Brazil.
Luis A RomanoMarine Station of Aquaculture, Oceanography Institute, Federal University of Rio Grande, Rio Grande, RS, 96 201-900, Brazil.
Marta C KlosterhoffMarine Station of Aquaculture, Oceanography Institute, Federal University of Rio Grande, Rio Grande, RS, 96 201-900, Brazil.
Luis E M NeryMolecular Biology Laboratory, Biological Sciences Institute (ICB), Federal University of Rio Grande-FURG, Rio Grande, RS, 96203-900, Brazil.
Rodrigo MaggioniCenter of Studies and Diagnosis of Aquatic Organism Diseases (CEDECAM), Marine Sciences Institute, Federal University of Ceara, Fortaleza, CE, 60165-081, Brazil.
Wilson WasieleskyMarine Station of Aquaculture, Oceanography Institute, Federal University of Rio Grande, Rio Grande, RS, 96 201-900, Brazil.
Luis F MarinsMolecular Biology Laboratory, Biological Sciences Institute (ICB), Federal University of Rio Grande-FURG, Rio Grande, RS, 96203-900, Brazil. dqmluf@furg.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The method usually employed to stimulate gonadal maturation and spawning of captive shrimp involves unilateral eyestalk ablation, which results in the removal of the endocrine complex responsible for gonad-inhibiting hormone (GIH) synthesis and release. In the present study, RNAi technology was used to inhibit transcripts of GIH in Litopenaeus vannamei females. The effect of gene silencing on gonad development was assessed by analyzing the expression of GIH and vitellogenin, respectively, in the eyestalk and ovaries of L. vannamei females, following ablation or injection with dsRNA-GIH, dsRNA-IGSF4D (non-related dsRNA), or saline solution. Histological analyses were performed to determine the stage of gonadal development and to assess the diameter of oocytes throughout the experimental procedure. Only oocytes at pre-vitellogenesis and primary vitellogenesis stages were identified in females injected with dsRNA-GIH, dsRNA-IGSF4D, or saline solution. Oocytes at all developmental stages were observed in eyestalk-ablated females, with predominance of later stages, such as secondary vitellogenesis and mature oocytes. Despite achieving 64, 73, and 71% knockdown of eyestalk GIH mRNA levels by 15, 30, and 37 days post-injection (dpi), respectively, in dsRNA-GIH-injected females, the expected increase in ovary vitellogenin mRNA expression was only observed on the 37th dpi. This is the first report of the use of RNAi technology to develop an alternative method to eyestalk ablation in captive L. vannamei shrimps.

Indexed as

RNA InterferenceAnimalsCarrier ProteinsFemaleGene Knockdown TechniquesGene SilencingInvertebrate HormonesOvaryOvulation InductionPenaeidaeTranscription FactorsVitellogenesisCarrier ProteinsInvertebrate HormonesTranscription Factorsvitellogenesis inhibiting hormoneGIHLitopenaeus vannameiReproductionRNAiRT-qPCR

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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.