Cited by 811

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

miRNA-Mediated Gene Silencing by Translational Repression Followed by mRNA Deadenylation and Decay

Djuranovic, Sergej, Nahvi, Ali, Green, Rachel·2012·Science

Abstract

Translation Block: MicroRNAs (miRNAs) are small, noncoding RNA genes that are found in the genomes of most eukaryotes, where they play an important role in the regulation of gene expression. Although whether gene activity is repressed by blocking translation of messenger RNA (mRNA) targets, or by promoting their deadenylation and then degradation, has been open to debate. Bazzini et al. (p. 233 , published online 15 March) and Djuranovic et al. (p. 237 ) looked at early points in the repression reaction in the zebrafish embryo or in Drosophila tissue culture cells, respectively, and found that translation was blocked before target mRNAs were significantly deadenylated and degraded. Thus, miRNAs appear to interfere with the initiation step of translation.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1126/science.1215691

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • miRNAs are excised from larger stem-loop-containing transcripts and incorporated into argonaute (Ago) proteins, generating functional entities capable of silencing target transcripts via translational repression and mRNA destabilization.

    “miRNAs are excised from larger stem-loop-containing transcripts and are subsequently incorporated into argonaute (Ago) proteins. This generates functional entities capable of silencing target transcripts via translational repression and mRNA destabilization (Bazzini et al., 2012; Djuranovic et al., 2012).”

    From Transcriptome-wide Discovery of microRNA Binding Sites in Human Brain (2014) · cites this paper as Djuranovic et al., 2012

  • Mature miRNAs bind to the 3′-untranslated region (UTR) sequence of target genes to form RNA-induced silencing complexes that influence protein synthesis by regulating gene transcription or degrading cytoplasmic messenger RNAs (mRNAs).

    “Mature miRNAs bind to the 3′-untranslated region (UTR) sequence of target genes to form RNA-induced silencing complexes that influence protein synthesis by regulating gene transcription or degrading cytoplasmic messenger RNAs (mRNAs)”

    From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Djuranovic et al., 2012

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 29

  1. 10.1016/j.cell.2009.01.002 · DOI · Paper page
  2. 10.1016/j.cell.2005.07.031 · DOI
  3. 10.1038/nature03315 · DOI · Paper page
  4. 10.1126/science.1122689 · DOI · Paper page
  5. 10.1261/rna.1399509 · DOI
  6. 10.1371/journal.pone.0006783 · DOI
  7. 10.1006/dbio.1999.9523 · DOI · Paper page
  8. 10.1126/science.1115079 · DOI
  9. 10.1016/j.molcel.2006.01.031 · DOI
  10. 10.1038/emboj.2008.275 · DOI
  11. 10.1038/nature09267 · DOI · Paper page
  12. 10.1073/pnas.0510928103 · DOI
  13. 10.1101/gad.1566707 · DOI
  14. 10.1126/science.1146067 · DOI
  15. 10.1016/j.molcel.2009.09.009 · DOI
  16. 10.1016/j.molcel.2009.08.004 · DOI
  17. 10.1101/gad.3.6.882 · DOI
  18. 10.1261/rna.1565109 · DOI
  19. 10.1101/gad.1424106 · DOI
  20. 10.1101/gad.1301805 · DOI
  21. 10.1101/gad.5.11.2108 · DOI · Paper page
  22. 10.1261/rna.569407 · DOI · Paper page
  23. Muckenthaler M., Gunkel N., Stripecke R., Hentze M. W., Regulated poly(A) tail shortening in somatic cells mediated by cap-proximal translational repressor proteins and ribosome association. RNA 3, 983 (1997).9292498
  24. 10.1016/j.molcel.2009.02.010 · DOI
  25. 10.1038/nrg2438 · DOI
  26. 10.1016/j.molcel.2011.09.007 · DOI
  27. 10.1038/nsmb.2166 · DOI
  28. 10.1038/nsmb.2149 · DOI · Paper page
  29. 10.1038/embor.2010.169 · DOI

Cited by

Sorted by citations

Metadata

Authors
Djuranovic, S., Nahvi, A., & Green, R.
Affiliations
Howard Hughes Medical Institute (HHMI) and Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Venue
Science
Published
2012-04-13
Volume
336
Issue
6078
Pages
237-240
ISSN
  • 0036-8075
  • 1095-9203
Cited by
811
References
1
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review