Molecular, genetic and evolutionary analysis of a paracentric inversion in Arabidopsis thaliana

Open Access
Authors
  • P. Fransz ORCID logo
  • G. Linc
  • C.-R. Lee
  • S. Alves Aflitos
  • J.R. Lasky
  • C. Toomajian
  • H. Ali
  • J. Peters
  • P. van Dam
  • X. Ji
  • M. Kuzak
  • T. Gerats
  • I. Schubert
  • K. Schneeberger
  • V. Colot
  • R. Martienssen
  • M. Koornneef
  • M. Nordborg
  • T.E. Juenger
  • H. de Jong
  • M.E. Schranz
Publication date 10-2016
Journal Plant Journal
Volume | Issue number 88 | 2
Pages (from-to) 159-178
Number of pages 20
Organisations
  • Faculty of Science (FNWI) - Swammerdam Institute for Life Sciences (SILS)
Abstract

Chromosomal inversions can provide windows onto the cytogenetic, molecular, evolutionary and demographic histories of a species. Here we investigate a paracentric 1.17-Mb inversion on chromosome 4 of Arabidopsis thaliana with nucleotide precision of its borders. The inversion is created by Vandal transposon activity, splitting an F-box and relocating a pericentric heterochromatin segment in juxtaposition with euchromatin without affecting the epigenetic landscape. Examination of the RegMap panel and the 1001 Arabidopsis genomes revealed more than 170 inversion accessions in Europe and North America. The SNP patterns revealed historical recombinations from which we infer diverse haplotype patterns, ancient introgression events and phylogenetic relationships. We find a robust association between the inversion and fecundity under drought. We also find linkage disequilibrium between the inverted region and the early flowering Col-FRIGIDA allele. Finally, SNP analysis elucidates the origin of the inversion to South-Eastern Europe approximately 5000 years ago and the FRI-Col allele to North-West Europe, and reveals the spreading of a single haplotype to North America during the 17th to 19th century. The 'American haplotype' was identified from several European localities, potentially due to return migration.

Document type Article
Note With supporting information
Language English
Published at https://doi.org/10.1111/tpj.13262
Downloads
tpj13262-sup-0001-FigS1 (Other version)
tpj13262-sup-0002-FigS2 (Other version)
tpj13262-sup-0003-FigS3 (Other version)
tpj13262-sup-0004-FigS4 (Other version)
tpj13262-sup-0005-FigS5 (Other version)
tpj13262-sup-0006-FigS6 (Other version)
tpj13262-sup-0007-FigS7 (Other version)
tpj13262-sup-0008-FigS8 (Other version)
tpj13262-sup-0009-FigS9 (Other version)
tpj13262-sup-0010-FigS10 (Other version)
tpj13262-sup-0011-FigS11 (Other version)
tpj13262-sup-0012-FigS12 (Other version)
tpj13262-sup-0013-FigS13 (Other version)
tpj13262-sup-0014-TableS1 (Other version)
tpj13262-sup-0015-TableS2 (Other version)
tpj13262-sup-0016-TableS3 (Other version)
tpj13262-sup-0017-TableS4 (Other version)
tpj13262-sup-0018-TableS5 (Other version)
tpj13262-sup-0019-TableS6 (Other version)
tpj13262-sup-0020-Legends (Other version)
Permalink to this page
Back