Evidence map›Paper›PMID 41878771›Full record

ArticleGenetics2026

The selective dynamics of interruptions at short tandem repeats.

Michael E Goldberg, Harriet Dashnow, Kelley Harris, Aaron R Quinlan

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

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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

1 citing paper in PubMed.

  1. 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.

Michael E GoldbergDepartment of Human Genetics, University of Utah, 15 N 2030 E, Salt Lake City, UT 84112, United States.ORCID 0000-0003-3310-6349
Harriet DashnowDepartment of Human Genetics, University of Utah, 15 N 2030 E, Salt Lake City, UT 84112, United States.ORCID 0000-0001-8433-6270
Kelley HarrisDepartment of Genome Sciences, University of Washington, 3720 15th Ave NE, Seattle, WA 98195, United States.ORCID 0000-0003-0302-2523
Aaron R QuinlanDepartment of Human Genetics, University of Utah, 15 N 2030 E, Salt Lake City, UT 84112, United States.

Funding

GEMS: Genomic approach to connecting Elevated germline Mutation rates with male infertility and Somatic healthR01HD106112 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI ASTON, KENNETH IVAN, HOTALING, JAMES · 2021 to 2025
$3.8M
New algorithms and tools for large-scale genomic analysesR01HG012252 · NHGRI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Aaron R Quinlan · 2022 to 2026
$3.2M
Training Program in Genomic MedicineT32HG008962 · NHGRI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Lynn Jorde, Aaron R Quinlan · 2016 to 2026
$3.0M
Investigating the landscape and genetic architecture of germline mutagenesisR35GM133428 · NIGMS · UNIVERSITY OF WASHINGTON · PI Kelley Harris · 2019 to 2026
$2.8M
Revealing new short tandem repeat variation in the human population across sequencing technologies: towards rare disease diagnosis and discoveryR00HG012796 · NHGRI · UNIVERSITY OF COLORADO DENVER · PI Harriet Dashnow · 2024 to 2026
$747k
NHGRI NIH HHS R00 HG012796NHGRI NIH HHS R01 HG012252NHGRI NIH HHS T32 HG008962NICHD NIH HHS R01 HD106112NIGMS NIH HHS R35 GM133428
6 · The paper itself

Abstract

Short tandem repeats (STRs) are hotspots of genomic instability that mutate at rates orders of magnitude greater than nonrepetitive loci due to frequent replication slippage. Expansions at some STR loci cause Mendelian diseases, while variation at other noncoding loci may affect complex traits, possibly by altering transcription factor occupancy of nearby binding sites. Accordingly, some STRs are inferred to be under purifying selection, regardless of their instability. One or more "interruptions", or bases that disrupt the locus's canonical repeat, significantly decrease an STR's mutability. For example, the onset of Huntington's Disease, a neurodegenerative disorder associated with somatic expansions of a trinucleotide coding STR, is delayed in individuals whose inherited alleles contain interruptions. Thus, interruptions that decrease mutation rate at some coding loci may broadly protect against deleterious phenotypes associated with locus instability. However, interruptions may themselves be deleterious at constrained loci, particularly at noncoding loci in gene regulatory elements, possibly disrupting the formation of secondary structures key to their function. We therefore hypothesized that the frequency of interruptions could depend on a locus's functional importance-at constrained loci, the fitness effects of expansions but also interruptions could be more deleterious than at neutral loci. To test this hypothesis, we examined the distribution of interruptions at ∼650,000 autosomal STRs. In the ∼2,500 3- or 6bp-motif coding STRs, we find that synonymous interruption density increases with purifying selection on the gene, while the opposite is true for missense-causing interruptions. In contrast, noncoding STRs in gene regulatory elements harbor fewer interruptions than elements that are unassociated with gene regulation and thus more likely to be evolving neutrally. Our findings indicate that the abundance of interruptions may be partially explained at coding STRs by the benefit of lower instability, whereas maintaining a core stretch of uninterrupted repeat may be key to the function of regulatory noncoding STRs, outweighing the benefits of stability.

Indexed as

Microsatellite RepeatsSelection, GeneticGenomic InstabilityHumansMutation Rateevolutionary genomicsmutationrepetitive elements

Identifiers

PMID41878771
PMCPMC13147528

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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.