Evidence map›Paper›PMID 25865001›Full record

ReviewJournal of inorganic biochemistry2015

Caged oligonucleotides for studying biological systems.

Brittani K Ruble, Sean B Yeldell, Ivan J Dmochowski

Abstract readReview
In one paragraph

Review in Journal of inorganic biochemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Photocleavable Guide crRNAs for a Light-Controllable CRISPR/Cas9 System.International journal of molecular sciences · 2024
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Conditionally Activated ("Caged") Oligonucleotides.Molecules (Basel, Switzerland) · 2021
    Review
  9. Review
  10. Review
  11. Multimerized self-assembled cagedChemical science · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Optochemical Control of Biological Processes in Cells and Animals.Angewandte Chemie (International ed. in English) · 2018
    Review
  16. Review
  17. Article
  18. Magnetic Field-Activated Sensing of mRNA in Living Cells.Journal of the American Chemical Society · 2017
    Article
  19. Review
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

3 authors.

Brittani K RubleDepartment of Chemistry, University of Pennsylvania, 231S. 34th Street, Philadelphia, PA 19104, United States.
Sean B YeldellDepartment of Chemistry, University of Pennsylvania, 231S. 34th Street, Philadelphia, PA 19104, United States.
Ivan J DmochowskiDepartment of Chemistry, University of Pennsylvania, 231S. 34th Street, Philadelphia, PA 19104, United States. Electronic address: ivandmo@sas.upenn.edu.

Funding

Oligonucleotides for turning genes on and off with lightR01GM083030 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI DMOCHOWSKI, IVAN JULIAN · 2008 to 2017
$3.0M
NIGMS NIH HHS R-01 GM083030NIGMS NIH HHS R01 GM083030
6 · The paper itself

Abstract

Light-activated ("caged") compounds have been widely employed for studying biological processes with high spatial and temporal control. In the past decade, several new approaches for caging the structure and function of DNA and RNA oligonucleotides have been developed. This review focuses on caged oligonucleotides that incorporate site-specifically one or two photocleavable linkers, whose photolysis yields oligonucleotides with dramatic structural and functional changes. This technique has been employed by our laboratory and others to photoregulate gene expression in cells and living organisms, typically using near UV-activated organic chromophores. To improve capabilities for in vivo studies, we harnessed the rich inorganic photochemistry of ruthenium bipyridyl complexes to synthesize Ru-caged morpholino antisense oligonucleotides that remain inactive in zebrafish embryos until uncaged with visible light. Expanding into new caged oligonucleotide applications, our lab has developed Transcriptome In Vivo Analysis (TIVA) technology, which provides the first noninvasive, unbiased method for isolating mRNA from single neurons in brain tissues. TIVA-isolated mRNA can be amplified and then analyzed using next-generation sequencing (RNA-seq).

Indexed as

AnimalsBrainCoordination ComplexesEmbryo, NonmammalianGene Expression ProfilingHumansLightMicroRNAsNucleic Acid ConformationNucleic Acid HybridizationOligonucleotides, AntisenseRNA, MessengerRutheniumZebrafishCoordination ComplexesMicroRNAsOligonucleotides, AntisenseRNA, MessengerRutheniumCaging chemistryLight-activated oligonucleotidesRuthenium photolinkersTranscriptome In Vivo Analysis

Identifiers

PMID25865001
PMCPMC4586300

What OpenQuestion holds

Textmetadata
LicenceTDM
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.