» Articles » PMID: 36195344

Natural Variation in Short Tandem Repeats

Overview
Journal Genome Res
Specialty Genetics
Date 2022 Oct 4
PMID 36195344
Authors
Affiliations
Soon will be listed here.
Abstract

Short tandem repeats (STRs) represent an important class of genetic variation that can contribute to phenotypic differences. Although millions of single nucleotide variants (SNVs) and short indels have been identified among wild strains, the natural diversity in STRs remains unknown. Here, we characterized the distribution of 31,991 STRs with motif lengths of 1-6 bp in the reference genome of Of these STRs, 27,667 harbored polymorphisms across 540 wild strains and only 9691 polymorphic STRs (pSTRs) had complete genotype data for more than 90% of the strains. Compared with the reference genome, the pSTRs showed more contraction than expansion. We found that STRs with different motif lengths were enriched in different genomic features, among which coding regions showed the lowest STR diversity and constrained STR mutations. STR diversity also showed similar genetic divergence and selection signatures among wild strains as in previous studies using SNVs. We further identified STR variation in two mutation accumulation line panels that were derived from two wild strains and found background-dependent and fitness-dependent STR mutations. We also performed the first genome-wide association analyses between natural variation in STRs and organismal phenotypic variation among wild strains. Overall, our results delineate the first large-scale characterization of STR variation in wild strains and highlight the effects of selection on STR mutations.

Citing Articles

Epigenetic gene silencing in plants: Insights from triplet repeat expansion in Arabidopsis.

Gu J, Noor I, Yang X, Sohail H Funct Integr Genomics. 2024; 24(5):176.

PMID: 39340544 DOI: 10.1007/s10142-024-01463-3.


The pan-tandem repeat map highlights multiallelic variants underlying gene expression and agronomic traits in rice.

He H, Leng Y, Cao X, Zhu Y, Li X, Yuan Q Nat Commun. 2024; 15(1):7291.

PMID: 39181885 PMC: 11344853. DOI: 10.1038/s41467-024-51854-0.


Pervasive conservation of intron number and other genetic elements revealed by a chromosome-level genomic assembly of the hyper-polymorphic nematode .

Teterina A, Willis J, Baer C, Phillips P bioRxiv. 2024; .

PMID: 38979286 PMC: 11230420. DOI: 10.1101/2024.06.25.600681.


SUMO protease FUG1, histone reader AL3 and chromodomain protein LHP1 are integral to repeat expansion-induced gene silencing in Arabidopsis thaliana.

Sureshkumar S, Bandaranayake C, Lv J, Dent C, Bhagat P, Mukherjee S Nat Plants. 2024; 10(5):749-759.

PMID: 38641663 DOI: 10.1038/s41477-024-01672-5.


A nematode model to evaluate microdeletion phenotype expression.

Antkowiak K, Coskun P, Noronha S, Tavella D, Massi F, Ryder S G3 (Bethesda). 2023; 14(2).

PMID: 37956108 PMC: 10849325. DOI: 10.1093/g3journal/jkad258.


References
1.
Evans K, Wit J, Stevens L, Hahnel S, Rodriguez B, Park G . Two novel loci underlie natural differences in Caenorhabditis elegans abamectin responses. PLoS Pathog. 2021; 17(3):e1009297. PMC: 7993787. DOI: 10.1371/journal.ppat.1009297. View

2.
Li H, Durbin R . Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009; 25(14):1754-60. PMC: 2705234. DOI: 10.1093/bioinformatics/btp324. View

3.
Saxena A, Salomon M, Matsuba C, Yeh S, Baer C . Evolution of the Mutational Process under Relaxed Selection in Caenorhabditis elegans. Mol Biol Evol. 2018; 36(2):239-251. PMC: 6367967. DOI: 10.1093/molbev/msy213. View

4.
Chang C, Chow C, Tellier L, Vattikuti S, Purcell S, Lee J . Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience. 2015; 4:7. PMC: 4342193. DOI: 10.1186/s13742-015-0047-8. View

5.
Crombie T, Zdraljevic S, Cook D, Tanny R, Brady S, Wang Y . Deep sampling of Hawaiian reveals high genetic diversity and admixture with global populations. Elife. 2019; 8. PMC: 6927746. DOI: 10.7554/eLife.50465. View