Evidence map›Paper›PMID 40624398›Full record

ArticleEuropean journal of human genetics : EJHG2025

Interrupted CTG repeats in the 37-43 units size range in the 3'UTR of DMPK are common alleles.

Hilde Swinkels, Maike Leferink, Maartje Pennings, Bart van der Sanden, Christian Gilissen, Jordi Corominas Galbany, Erik-Jan Kamsteeg

Abstract read
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Article in European journal of human genetics : EJHG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Insights in genetics: from molecular mechanisms to patient perspectives.European journal of human genetics : EJHG · 2025
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Hilde SwinkelsDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
Maike LeferinkDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
Maartje PenningsDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID 0000-0001-5485-7497
Bart van der SandenDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID 0000-0003-0546-1351
Christian GilissenDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID 0000-0003-1693-9699
Jordi Corominas GalbanyDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
Erik-Jan KamsteegDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands. Erik-Jan.kamsteeg@radboudumc.nl.ORCID 0000-0001-6480-1892

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The size of non-pathogenic CTG repeats in the 3'UTR of the DMPK gene varies from 5-35, whereas repeats over 50 units are pathogenic. The Intermediate repeats of 36-50 are considered 'premutation', as they are present in individuals unaffected by myotonic dystrophy, but are prone to further enlargement into the pathogenic range upon transmission to offspring. In this study, we showed that CCGCTG interrupted intermediate repeats, in the repeat size of 37-43 units, have been detected in multiple families with a history of myotonic dystrophy. However, segregation and microsatellite marker analysis of these interrupted intermediate alleles revealed that these alleles are not the same alleles (haplotypes) that were found expanded in affected family members. In contrast to the pure intermediate alleles, the CCGCTG intermediate repeats within families did not show intergenerational variability in size. Furthermore, we showed that the CCGCTG interrupted intermediate alleles have an allele frequency of approximately 0.35% in the general population, while CCGCTG interruptions were not detected in pathogenic repeat expansions over 50 repeat units in our control cohort. We postulate that intermediate repeats of size 37-43 having CCGCTG interruptions are not prone to further expansion, and therefore not act as premutations, which has great relevance for individuals with these alleles and has implications for genetic counseling and testing.

Indexed as

3' Untranslated RegionsAllelesMyotonic DystrophyProtein Serine-Threonine KinasesTrinucleotide Repeat ExpansionFemaleGene FrequencyHaplotypesHumansMaleMicrosatellite RepeatsMyotonin-Protein KinasePedigree3' Untranslated RegionsDMPK protein, humanMyotonin-Protein KinaseProtein Serine-Threonine Kinases

Identifiers

PMID40624398
PMCPMC12583562

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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.