Evidence map›Paper›PMID 12466025›Full record

ArticleBMC biotechnology2002

Group I aptazymes as genetic regulatory switches.

Kristin M Thompson, Heather A Syrett, Scott M Knudsen, Andrew D Ellington

Open access · goldAbstract read
In one paragraph

Article in BMC biotechnology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

37 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Supernova: A Deoxyribozyme that Catalyzes a Chemiluminescent Reaction.Angewandte Chemie (International ed. in English) · 2022
    Article
  5. Article
  6. Review
  7. The case of the missing allosteric ribozymes.Nature chemical biology · 2021
    Review
  8. Article
  9. Imaginary Ribozymes.ACS chemical biology · 2020
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Computational analysis of riboswitch-based regulation.Biochimica et biophysica acta · 2014
    Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Kristin M ThompsonDepartment of Chemistry and Biochemistry, Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, TX 78712, USA. kthompson@archemix.com
Heather A Syrett
Scott M Knudsen
Andrew D Ellington
The University of Texas at Austin · US

Funding

Ribozymes for Peptide- and Protein- Sensing Chip ArraysR01GM061789 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI ELLINGTON, ANDREW D · 2001 to 2002
$459k
NIGMS NIH HHS 1R01 GM61789-01NIGMS NIH HHS R01 GM061789
6 · The paper itself

Abstract

backgroundAllosteric ribozymes (aptazymes) that have extraordinary activation parameters have been generated in vitro by design and selection. For example, hammerhead and ligase ribozymes that are activated by small organic effectors and protein effectors have been selected from random sequence pools appended to extant ribozymes. Many ribozymes, especially self-splicing introns, are known control gene regulation or viral replication in vivo. We attempted to generate Group I self-splicing introns that were activated by a small organic effector, theophylline, and to show that such Group I aptazymes could mediate theophylline-dependent splicing in vivo.

resultsBy appending aptamers to the Group I self-splicing intron, we have generated a Group I aptazyme whose in vivo splicing is controlled by exogenously added small molecules. Substantial differences in gene regulation could be observed with compounds that differed by as little as a single methyl group. The effector-specificity of the Group I aptazyme could be rationally engineered for new effector molecules.

conclusionGroup I aptazymes may find applications as genetic regulatory switches for generating conditional knockouts at the level of mRNA or for developing economically viable gene therapies.

Indexed as

Allosteric RegulationBacteriophage T4Base SequenceEnzyme ActivationGene Expression Regulation, EnzymologicIntronsMolecular Sequence DataNucleic Acid ConformationRNA, CatalyticRNA, Ribosomal, Self-SplicingRNA SplicingRNA, ViralSubstrate SpecificityThymidylate SynthaseViral ProteinsRNA, CatalyticRNA, Ribosomal, Self-SplicingRNA, ViralThymidylate SynthaseViral Proteins

Identifiers

PMID12466025
PMCPMC139998
OpenAlexW1950531847

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.