Evidence map›Paper›PMID 25123664›Full record

ArticleNucleic acids research2014

Structural basis of lariat RNA recognition by the intron debranching enzyme Dbr1.

Eric J Montemayor, Adam Katolik, Nathaniel E Clark, Alexander B Taylor, Jonathan P Schuermann, D Joshua Combs, Richard Johnsson, Stephen P Holloway, Scott W Stevens, Masad J Damha and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

32 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Solid Phase Chemical Synthesis of RNA.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Perspectives on Circular RNAs as Prostate Cancer Biomarkers.Frontiers in cell and developmental biology · 2020
    Review
  17. Influenza Pathogenesis: The Effect of Host Factors on Severity of Disease.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Review
  18. Article
  19. Unexplored Molecular Features of theFrontiers in cellular and infection microbiology · 2018
    Article
  20. Life and Death of mRNA Molecules inFrontiers in cellular and infection microbiology · 2018
    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

11 authors at 4 institutions in 2 countries.

Eric J MontemayorDepartment of Biochemistry, The University of Texas Health Science Center, San Antonio, TX 78229, USA X-ray Crystallography Core Laboratory, The University of Texas Health Science Center, San Antonio, TX 78229, USA.
Adam KatolikDepartment of Chemistry, McGill University, Montreal, Quebec H3A 0B8, Canada.
Nathaniel E ClarkDepartment of Biochemistry, The University of Texas Health Science Center, San Antonio, TX 78229, USA X-ray Crystallography Core Laboratory, The University of Texas Health Science Center, San Antonio, TX 78229, USA.
Alexander B TaylorDepartment of Biochemistry, The University of Texas Health Science Center, San Antonio, TX 78229, USA X-ray Crystallography Core Laboratory, The University of Texas Health Science Center, San Antonio, TX 78229, USA.
Jonathan P SchuermannNortheastern Collaborative Access Team, Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA.
D Joshua CombsProgram in Cellular and Molecular Biology, University of Texas at Austin, Austin, TX 78212, USA.
Richard JohnssonDepartment of Chemistry, McGill University, Montreal, Quebec H3A 0B8, Canada.
Stephen P HollowayDepartment of Biochemistry, The University of Texas Health Science Center, San Antonio, TX 78229, USA.
Scott W StevensDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, TX 78712, USA scott.stevens@austin.utexas.edu.
Masad J DamhaDepartment of Chemistry, McGill University, Montreal, Quebec H3A 0B8, Canada masad.damha@mcgill.ca.
P John HartDepartment of Biochemistry, The University of Texas Health Science Center, San Antonio, TX 78229, USA X-ray Crystallography Core Laboratory, The University of Texas Health Science Center, San Antonio, TX 78229, USA Geriatric Research, Education, and Clinical Center, Department of Veterans Affairs, South Texas Veterans Health Care System, San Antonio, TX 78229, USA pjhart1@biochem.uthscsa.edu.ORCID http://orcid.org/0000-0003-1097-3992
The University of Texas Health Science Center at San Antonio · USMcGill University · CAThe University of Texas at Austin · USCornell University · US

Funding

Overall EvaluationP41GM103403 · NIGMS · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2012 to 2017
$14.3M
TRAINING GRANT ON THE BIOLOGY OF AGINGT32AG021890 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Erzsebet Kokovay, JAMES FLOYD NELSON · 2003 to 2026
$11.4M
Spliceosome disassembly and intron turnoverR01GM084246 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI STEVENS, SCOTT W · 2009 to 2012
$1.2M
The Intron Debranching Enzyme (Dbr1) in Amyotrophic Lateral SclerosisI01BX002580 · VA · SOUTH TEXAS VETERANS HEALTH CARE SYSTEM · PI HART, PETER JOHN · 2015 to 2018
–
BLRD VA I01 BX002580NIA NIH HHS 5 T32 AG021890NIGMS NIH HHS GM084246NIGMS NIH HHS P41 GM103403
6 · The paper itself

Abstract

The enzymatic processing of cellular RNA molecules requires selective recognition of unique chemical and topological features. The unusual 2',5'-phosphodiester linkages in RNA lariats produced by the spliceosome must be hydrolyzed by the intron debranching enzyme (Dbr1) before they can be metabolized or processed into essential cellular factors, such as snoRNA and miRNA. Dbr1 is also involved in the propagation of retrotransposons and retroviruses, although the precise role played by the enzyme in these processes is poorly understood. Here, we report the first structures of Dbr1 alone and in complex with several synthetic RNA compounds that mimic the branchpoint in lariat RNA. The structures, together with functional data on Dbr1 variants, reveal the molecular basis for 2',5'-phosphodiester recognition and explain why the enzyme lacks activity toward 3',5'-phosphodiester linkages. The findings illuminate structure/function relationships in a unique enzyme that is central to eukaryotic RNA metabolism and set the stage for the rational design of inhibitors that may represent novel therapeutic agents to treat retroviral infections and neurodegenerative disease.

Indexed as

IntronsEntamoeba histolyticaModels, MolecularNucleic Acid ConformationProtein Structure, TertiaryRNARNA NucleotidyltransferasesRNARNA Nucleotidyltransferases

Identifiers

PMID25123664
PMCPMC4176325
OpenAlexW2154396157

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.