Atlas of telomeric repeat diversity in Arabidopsis thaliana.


Journal

Genome biology
ISSN: 1474-760X
Titre abrégé: Genome Biol
Pays: England
ID NLM: 100960660

Informations de publication

Date de publication:
16 Sep 2024
Historique:
received: 29 01 2024
accepted: 03 09 2024
medline: 17 9 2024
pubmed: 17 9 2024
entrez: 16 9 2024
Statut: epublish

Résumé

Telomeric repeat arrays at the ends of chromosomes are highly dynamic in composition, but their repetitive nature and technological limitations have made it difficult to assess their true variation in genome diversity surveys. We have comprehensively characterized the sequence variation immediately adjacent to the canonical telomeric repeat arrays at the very ends of chromosomes in 74 genetically diverse Arabidopsis thaliana accessions. We first describe several types of distinct telomeric repeat units and then identify evolutionary processes such as local homogenization and higher-order repeat formation that shape diversity of chromosome ends. By comparing largely isogenic samples, we also determine repeat number variation of the degenerate and variant telomeric repeat array at both the germline and somatic levels. Finally, our analysis of haplotype structure uncovers chromosome end-specific patterns in the distribution of variant telomeric repeats, and their linkage to the more proximal non-coding region. Our findings illustrate the spectrum of telomeric repeat variation at multiple levels in A. thaliana-in germline and soma, across all chromosome ends, and across genetic groups-thereby expanding our knowledge of the evolution of chromosome ends.

Sections du résumé

BACKGROUND BACKGROUND
Telomeric repeat arrays at the ends of chromosomes are highly dynamic in composition, but their repetitive nature and technological limitations have made it difficult to assess their true variation in genome diversity surveys.
RESULTS RESULTS
We have comprehensively characterized the sequence variation immediately adjacent to the canonical telomeric repeat arrays at the very ends of chromosomes in 74 genetically diverse Arabidopsis thaliana accessions. We first describe several types of distinct telomeric repeat units and then identify evolutionary processes such as local homogenization and higher-order repeat formation that shape diversity of chromosome ends. By comparing largely isogenic samples, we also determine repeat number variation of the degenerate and variant telomeric repeat array at both the germline and somatic levels. Finally, our analysis of haplotype structure uncovers chromosome end-specific patterns in the distribution of variant telomeric repeats, and their linkage to the more proximal non-coding region.
CONCLUSIONS CONCLUSIONS
Our findings illustrate the spectrum of telomeric repeat variation at multiple levels in A. thaliana-in germline and soma, across all chromosome ends, and across genetic groups-thereby expanding our knowledge of the evolution of chromosome ends.

Identifiants

pubmed: 39285474
doi: 10.1186/s13059-024-03388-3
pii: 10.1186/s13059-024-03388-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

244

Subventions

Organisme : Novo Nordisk Fonden
ID : Novozymes Prize

Informations de copyright

© 2024. The Author(s).

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Auteurs

Yueqi Tao (Y)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany.

Wenfei Xian (W)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany.

Zhigui Bao (Z)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany.

Fernando A Rabanal (FA)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany.

Andrea Movilli (A)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany.

Christa Lanz (C)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany.

Gautam Shirsekar (G)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany.

Detlef Weigel (D)

Department of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen, 72076, Germany. weigel@weigelworld.org.

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Classifications MeSH