Evidence map›Paper›PMID 15525711›Full record

ArticleRNA (New York, N.Y.)2004

Generation of a catalytic module on a self-folding RNA.

Wataru Yoshioka, Yoshiya Ikawa, Luc Jaeger, Hideaki Shiraishi, Tan Inoue

Erratum issuedAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. RNA modularity for synthetic biology.F1000prime reports · 2013
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Emergence of a fast-reacting ribozyme that is capable of undergoing continuous evolution.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  13. Article
  14. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors.

Wataru YoshiokaGraduate School of Biostudies, Kyoto University, 606-8502 Japan.
Yoshiya Ikawa
Luc Jaeger
Hideaki Shiraishi
Tan Inoue

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is theoretically possible to obtain a catalytic site of an artificial ribozyme from a random sequence consisting of a limited numbers of nucleotides. However, this strategy has been inadequately explored. Here, we report an in vitro selection technique that exploits modular construction of a structurally constrained RNA to acquire a catalytic site for RNA ligation from a short random sequence. To practice the selection, a sequence of 30 nucleotides was located close to the putative reaction site in a derivative of a naturally occurring self-folding RNA whose crystal structure is known. RNAs whose activity depended on the starting three-dimensional structure were selected with 3'-5' ligation specificity, indicating that the strategy can be used to acquire a variety of catalytic sites and other functional RNA modules.

Indexed as

AnimalsBase SequenceCatalytic DomainModels, MolecularMolecular Sequence DataMutagenesis, Site-DirectedNucleic Acid ConformationRNARNA, CatalyticRNA, ProtozoanTetrahymenaRNARNA, CatalyticRNA, Protozoan

Identifiers

PMID15525711
PMCPMC1370678

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.