Evidence map›Paper›PMID 16269545›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

The structural basis of myotonic dystrophy from the crystal structure of CUG repeats.

Blaine H M Mooers, Jeremy S Logue, J Andrew Berglund

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

105 citing papers in PubMed, 186 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
  6. A pothole-filling strategy for selective targeting of rCUG-repeats associated with myotonic dystrophy type 1.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Review
  9. Article
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  12. Review
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  14. Article
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45 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Blaine H M MooersDepartment of Chemistry, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403-1229, USA.
Jeremy S Logue
J Andrew Berglund
Howard Hughes Medical Institute · US

Funding

STRUCTURE, FUNCTION, AND STABILITY OF T4 PHAGE LYSOZYMER01GM021967 · NIGMS · UNIVERSITY OF OREGON · PI MATTHEWS, BRIAN W · 1985 to 2008
$2.9M
Molecular Mechanisms of Myotonic DystrophyR01AR053903 · NIAMS · UNIVERSITY OF OREGON · PI BERGLUND, ANDREW · 2006 to 2010
$1.3M
X-RAY STRUCTURAL STUDIES OF PROTEINSR01GM020066 · NIGMS · UNIVERSITY OF OREGON · PI MATTHEWS, BRIAN W · 1985 to 2004
$1.2M
NIGMS NIH HHS GM21967NIGMS NIH HHS R01 GM020066NIGMS NIH HHS R01 GM021967
6 · The paper itself

Abstract

Myotonic dystrophy (DM) type 1 is associated with an expansion of (>50) CTG repeats within the 3' untranslated region (UTR) of the dystrophin myotonin protein kinase gene (dmpk). In the corresponding mRNA transcript, the CUG repeats form an extended stem-loop structure. The double-stranded RNA of the stem sequesters RNA binding proteins away from their normal cellular targets resulting in aberrant transcription, alternative splicing patterns, or both, thereby leading to DM. To better understand the structural basis of DM type 1, we determined to 1.58-A resolution the x-ray crystal structure of an 18-bp RNA containing six CUG repeats. The CUG repeats form antiparallel double-stranded helices that stack end-on-end in the crystal to form infinite, pseudocontinuous helices similar to the long CUG stem loops formed by the expanded CUG repeats in DM type 1. The CUG helix is very similar in structure to A-form RNA with the exception of the unique U-U mismatches. This structure provides a high-resolution view of a toxic, trinucleotide repeat RNA.

Indexed as

Trinucleotide Repeats3' Untranslated RegionsCrystallographyHydrogen BondingModels, MolecularMyotonic DystrophyMyotonin-Protein KinaseProtein ConformationProtein Serine-Threonine Kinases3' Untranslated RegionsMyotonin-Protein KinaseProtein Serine-Threonine Kinases

Identifiers

PMID16269545
PMCPMC1283809
OpenAlexW2159985046

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.