Chromosome-level assembly of Arabidopsis thaliana Ler reveals the extent of translocation and inversion polymorphisms
Resequencing or reference-based assemblies reveal large parts of the small-scale sequence variation. However, they typically fail to separate such local variation into colinear and rearranged variation, because they usually do not recover the complement of large-scale rearrangements, including trans...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 113; no. 28; pp. E4052 - E4060 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
12.07.2016
|
Series | PNAS Plus |
Subjects | |
Online Access | Get full text |
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Summary: | Resequencing or reference-based assemblies reveal large parts of the small-scale sequence variation. However, they typically fail to separate such local variation into colinear and rearranged variation, because they usually do not recover the complement of large-scale rearrangements, including transpositions and inversions. Besides the availability of hundreds of genomes of diverse Arabidopsis thaliana accessions, there is so far only one full-length assembled genome: the reference sequence. We have assembled 117 Mb of the A. thaliana Landsberg erecta (Ler) genome into five chromosome-equivalent sequences using a combination of short Illumina reads, long PacBio reads, and linkage information. Whole-genome comparison against the reference sequence revealed 564 transpositions and 47 inversions comprising ∼3.6 Mb, in addition to 4.1 Mb of nonreference sequence, mostly originating from duplications. Although rearranged regions are not different in local divergence from colinear regions, they are drastically depleted for meiotic recombination in heterozygotes. Using a 1.2-Mb inversion as an example, we show that such rearrangement-mediated reduction of meiotic recombination can lead to genetically isolated haplotypes in the worldwide population of A. thaliana. Moreover, we found 105 single-copy genes, which were only present in the reference sequence or the Ler assembly, and 334 single-copy orthologs, which showed an additional copy in only one of the genomes. To our knowledge, this work gives first insights into the degree and type of variation, which will be revealed once complete assemblies will replace resequencing or other reference-dependent methods. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Contributed by Maarten Koornneef, May 12, 2016 (sent for review February 18, 2016; reviewed by Ian R. Henderson and Yves Van de Peer) 3Present address: KWS SAAT SE, Research & Development-Data Management, 37574 Einbeck, Germany. Author contributions: M.K., S.O., and K.S. designed research; B.H. and D.B. performed research; L.Z., J.D., E.-M.W., W.-B.J., V.P., G.V.J., S.O., and K.S. analyzed data; and L.Z. and K.S. wrote the paper. 2Present address: Centre for Human Genetics, University Hospital Leuven, and Department of Human Genetics, KU Leuven, 3000 Leuven, Belgium. 4Present address: Rijk Zwaan Research & Development Fijnaart, Rijk Zwaan, 4793 RS, Fijnaart, The Netherlands. 1L.Z. and J.D. contributed equally to this work. Reviewers: I.R.H., University of Cambridge; and Y.V.d.P., Ghent University, Vlaams Instituut voor Biotechnologie. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.1607532113 |