Evidence map›Paper›PMID 28640690›Full record

ReviewRNA biology2017

A new layer of rRNA regulation by small interference RNAs and the nuclear RNAi pathway.

Xufei Zhou, Xiangyang Chen, Yun Wang, Xuezhu Feng, Shouhong Guang

Open access · bronzeAbstract readReview
In one paragraph

Review in RNA biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. The Versatile Applications of Antisense Oligonucleotides in Modern Medicine.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Non-Coding RNA-Driven Regulation of rRNA Biogenesis.International journal of molecular sciences · 2020
    Review
  10. Inhibition of retinal neovascularization by VEGF siRNA delivered via bioreducible lipid-like nanoparticles.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Erroneous ribosomal RNAs promote the generation of antisense ribosomal siRNA.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. 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

5 authors at 1 institution in 1 country.

Xufei Zhoua School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China , Hefei , Anhui , P.R. China.ORCID 0000-0001-7119-8390
Xiangyang Chena School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China , Hefei , Anhui , P.R. China.
Yun Wanga School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China , Hefei , Anhui , P.R. China.
Xuezhu Fenga School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China , Hefei , Anhui , P.R. China.
Shouhong Guanga School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China , Hefei , Anhui , P.R. China.
University of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribosome biogenesis drives cell growth and proliferation, but mechanisms that modulate this process remain poorly understood. For a long time, small rRNA sequences have been widely treated as non-specific degradation products and neglected as garbage sequences. Recently, we identified a new class of antisense ribosomal siRNAs (risiRNAs) that downregulate pre-rRNA through the nuclear RNAi pathway in C. elegans. risiRNAs exhibit sequence characteristics similar to 22G RNA while complement to 18S and 26S rRNA. risiRNAs elicit the translocation of the nuclear Argonaute protein NRDE-3 from the cytoplasm to nucleus and nucleolus, in which the risiRNA/NRDE complex binds to pre-rRNA and silences rRNA expression. Interestingly, when C. elegans is exposed to environmental stimuli, such as cold shock and ultraviolet illumination, risiRNAs accumulate and further turn on the nuclear RNAi-mediated gene silencing pathway. risiRNA may act in a quality control mechanism of rRNA homeostasis. When the exoribonuclease SUSI-1(ceDis3L2) is mutated, risiRNAs are dramatically increased. In this Point of View article, we will summarize our understanding of the small antisense ribosomal siRNAs in a variety of organisms, especially C. elegans, and their possible roles in the quality control mechanism of rRNA homeostasis.

Indexed as

RNA InterferenceActive Transport, Cell NucleusAnimalsArabidopsisCaenorhabditis elegansCaenorhabditis elegans ProteinsCell NucleusExoribonucleasesHomeostasisNeurospora crassaProtein BindingProtein TransportRibosomesRNA-Binding ProteinsRNA PrecursorsRNA, RibosomalCaenorhabditis elegans ProteinsExoribonucleasesNRDE-3 protein, C elegansRNA-Binding ProteinsRNA PrecursorsRNA, RibosomalRNA, Small InterferingNRDEnucleolusrisiRNArRNAstress

Identifiers

PMID28640690
PMCPMC5785222
OpenAlexW2686501960

What OpenQuestion holds

Textmetadata
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.