Evidence map›Paper›PMID 40796852›Full record

ArticleGenome biology2025

Mutations of short tandem repeats explain abundant trait heritability in Arabidopsis.

Zhi-Qin Zhang, Juan Jiang, Yong-Chao Xu, Craig Dent, Sridevi Sureshkumar, Sureshkumar Balasubramanian, Ya-Long Guo

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Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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9citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zhi-Qin Zhang *State Key Laboratory of Plant Diversity and Specialty Crops/State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Juan Jiang *State Key Laboratory of Plant Diversity and Specialty Crops/State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Yong-Chao XuState Key Laboratory of Plant Diversity and Specialty Crops/State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Craig DentSchool of Biological Sciences, Monash University, VIC, 3800, Australia.
Sridevi SureshkumarSchool of Biological Sciences, Monash University, VIC, 3800, Australia.
Sureshkumar BalasubramanianSchool of Biological Sciences, Monash University, VIC, 3800, Australia.
Ya-Long GuoState Key Laboratory of Plant Diversity and Specialty Crops/State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China. yalong.guo@ibcas.ac.cn.

Funding

ARC Discovery Project Grant DP190101479Australian Research Council (ARC) Future Fellowship FT190100403National Natural Science Foundation of China 32430008
6 · The paper itself

Abstract

backgroundShort tandem repeat (STR) mutations are major drivers of genetic variation and deeply influence phenotypic diversity and evolution, they are often overlooked despite their significant effects.

resultsHere, we leverage mutation accumulation lines descended from Col-0 accession of Arabidopsis thaliana to assess the variation in the repeat length of STRs (STR mutation rate). We find that STR mutation rate far exceeds single nucleotide polymorphisms rates. Interspecific comparison between A. thaliana and Arabidopsis lyrata reveals rapid STR turnover, with the most majority of the loci occurring only in A. thaliana. Intraspecific comparison of ten assembled A. thaliana genomes reveals that 29.3% of STRs display presence/absence variations, 36.5% show length variation, 21.2% have both types of variations, while only a small proportion have no variation. By association analysis, we find several STRs are associated with diverse phenotypes. Further analysis based on RNA-seq dataset from 413 accessions, we identify 3,871 expression-associated STRs and 651 splicing-associated STRs, of which over one thousand co-localized with known signals for diverse traits detected by genome-wide association studies. Notably, based on analysis of the expression levels of 24,175 genes and splice site strength values of 12,784 splice sites, as well as 16 phenotypes of natural A. thaliana populations, we determine the similar average heritability of these three trait sets explained by STR variation.

conclusionsOur results reveal the evolutionary dynamics of STRs, and highlight the importance of STR variation as an important contributor to missing heritability in regulating complex traits.

Indexed as

ArabidopsisMicrosatellite RepeatsMutationQuantitative Trait, HeritableGenome, PlantGenome-Wide Association StudyMutation RatePhenotypePolymorphism, Single NucleotideArabidopsis thalianaEvolutionMissing heritabilityMutation rateNatural variationShort tandem repeats

Identifiers

PMID40796852
PMCPMC12341274

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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.