Author
Listed:
- Xiangchao Gan
(Wellcome Trust Centre for Human Genetics, University of Oxford)
- Oliver Stegle
(Max Planck Institute for Intelligent Systems and Max Planck Institute for Developmental Biology, Spemannstraβe 38)
- Jonas Behr
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- Joshua G. Steffen
(University of Utah)
- Philipp Drewe
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- Katie L. Hildebrand
(Kansas State University)
- Rune Lyngsoe
(University of Oxford)
- Sebastian J. Schultheiss
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- Edward J. Osborne
(University of Utah)
- Vipin T. Sreedharan
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- André Kahles
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- Regina Bohnert
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- Géraldine Jean
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- Paul Derwent
(European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton)
- Paul Kersey
(European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton)
- Eric J. Belfield
(University of Oxford)
- Nicholas P. Harberd
(University of Oxford)
- Eric Kemen
(The Sainsbury Laboratory)
- Christopher Toomajian
(Kansas State University)
- Paula X. Kover
(University of Bath)
- Richard M. Clark
(University of Utah)
- Gunnar Rätsch
(Friedrich Miescher Laboratory, Max Planck Society, Spemannstraβe 39)
- Richard Mott
(Wellcome Trust Centre for Human Genetics, University of Oxford)
Abstract
Genetic differences between Arabidopsis thaliana accessions underlie the plant’s extensive phenotypic variation, and until now these have been interpreted largely in the context of the annotated reference accession Col-0. Here we report the sequencing, assembly and annotation of the genomes of 18 natural A. thaliana accessions, and their transcriptomes. When assessed on the basis of the reference annotation, one-third of protein-coding genes are predicted to be disrupted in at least one accession. However, re-annotation of each genome revealed that alternative gene models often restore coding potential. Gene expression in seedlings differed for nearly half of expressed genes and was frequently associated with cis variants within 5 kilobases, as were intron retention alternative splicing events. Sequence and expression variation is most pronounced in genes that respond to the biotic environment. Our data further promote evolutionary and functional studies in A. thaliana, especially the MAGIC genetic reference population descended from these accessions.
Suggested Citation
Xiangchao Gan & Oliver Stegle & Jonas Behr & Joshua G. Steffen & Philipp Drewe & Katie L. Hildebrand & Rune Lyngsoe & Sebastian J. Schultheiss & Edward J. Osborne & Vipin T. Sreedharan & André Kahles , 2011.
"Multiple reference genomes and transcriptomes for Arabidopsis thaliana,"
Nature, Nature, vol. 477(7365), pages 419-423, September.
Handle:
RePEc:nat:nature:v:477:y:2011:i:7365:d:10.1038_nature10414
DOI: 10.1038/nature10414
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Citations
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Cited by:
- Christina L Richards & Ulises Rosas & Joshua Banta & Naeha Bhambhra & Michael D Purugganan, 2012.
"Genome-Wide Patterns of Arabidopsis Gene Expression in Nature,"
PLOS Genetics, Public Library of Science, vol. 8(4), pages 1-14, April.
- Tamer Aldwairi & David J. Chevalier & Andy D. Perkins, 2021.
"Exploring the Effect of Climate Factors on SNPs within FHA Domain Genes in Eurasian Arabidopsis Ecotypes,"
Agriculture, MDPI, vol. 11(2), pages 1-10, February.
- Ryutaro Kobayashi & Yuri Ohkubo & Mai Izumi & Ryosuke Ota & Keiko Yamada & Yoko Hayashi & Yasuko Yamashita & Saki Noda & Mari Ogawa-Ohnishi & Yoshikatsu Matsubayashi, 2024.
"Integration of shoot-derived polypeptide signals by root TGA transcription factors is essential for survival under fluctuating nitrogen environments,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
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