Previous Article |
Table of Contents
| Next Article
BIOLOGICAL SCIENCES / PLANT BIOLOGY
Mechanisms of chromosome number reduction in Arabidopsis thaliana and related Brassicaceae species





*Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond TW9 3AB, United Kingdom;
Leibniz-Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstrasse 3, 06466 Gatersleben, Germany;
Max-Planck-Institut für Molekulare Pflanzenphysiologie, 14424 Potsdam, Germany; and ¶Allan Wilson Centre for Molecular Ecology and Evolution, Massey University, Palmerston North, New Zealand
Edited by Maarten Koornneef, Wageningen University and Research Centre, Wageningen, The Netherlands, and approved February 1, 2006 (received for review December 14, 2005)
Evolution of chromosome complements can be resolved by genome sequencing, comparative genetic mapping, and comparative chromosome painting. Previously, comparison of genetic maps and gene-based phylogenies suggested that the karyotypes of Arabidopsis thaliana (n = 5) and of related species with six or seven chromosome pairs were derived from an ancestral karyotype with eight chromosome pairs. To test this hypothesis, we applied multicolor chromosome painting using contiguous bacterial artificial chromosome pools of A. thaliana arranged according to the genetic maps of Arabidopsis lyrata and Capsella rubella (both n = 8) to A. thaliana, A. lyrata, Neslia paniculata, Turritis glabra, and Hornungia alpina. This approach allowed us to map the A. lyrata centromeres as a prerequisite to defining a putative ancestral karyotype (n = 8) and to elucidate the evolutionary mechanisms that shaped the karyotype of A. thaliana and its relatives. We conclude that chromosome "fusions" in A. thaliana resulted from (i) generation of acrocentric chromosomes by pericentric inversions, (ii) reciprocal translocation between two chromosomes (one or both acrocentric), and (iii) elimination of a minichromosome that arose in addition to the "fusion chromosome." Comparative chromosome painting applied to N. paniculata (n = 7), T. glabra (n = 6), and H. alpina (n = 6), for which genetic maps are not available, revealed chromosomal colinearity between all species tested and allowed us to reconstruct the evolution of their chromosomes from a putative ancestral karyotype (n = 8). Although involving different ancestral chromosomes, chromosome number reduction followed similar routes as found within the genus Arabidopsis.
chromosome painting | genome homeology | karyotype evolution | genome colinearity | phylogeny
Conflict of interest statement: No conflicts declared.
Data deposition: The sequences reported in this paper have been deposited in the GenBank database (accession nos. AF167571, M64119, AY198405, X52320, AP000423, and DQ310510DQ310545).
This paper was submitted directly (Track II) to the PNAS office.
To whom correspondence should be addressed at: Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, United Kingdom. E-mail: m.lysak{at}kew.org
© 2006 by The National Academy of Sciences of the USA
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg What's this?
This article has been cited by other articles in HighWire Press-hosted journals:
![]() |
H. Weiss-Schneeweiss, K. Tremetsberger, G. M. Schneeweiss, J. S. Parker, and T. F. Stuessy Karyotype Diversification and Evolution in Diploid and Polyploid South American Hypochaeris (Asteraceae) Inferred from rDNA Localization and Genetic Fingerprint Data Ann. Bot., May 1, 2008; 101(7): 909 - 918. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Lysak, K. Cheung, M. Kitschke, and P. Bures Ancestral Chromosomal Blocks Are Triplicated in Brassiceae Species with Varying Chromosome Number and Genome Size Plant Physiology, October 1, 2007; 145(2): 402 - 410. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Berr and I. Schubert Interphase Chromosome Arrangement in Arabidopsis thaliana Is Similar in Differentiated and Meristematic Tissues and Shows a Transient Mirror Symmetry After Nuclear Division Genetics, June 1, 2007; 176(2): 853 - 863. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Schranz, A. J. Windsor, B.-h. Song, A. Lawton-Rauh, and T. Mitchell-Olds Comparative Genetic Mapping in Boechera stricta, a Close Relative of Arabidopsis Plant Physiology, May 1, 2007; 144(1): 286 - 298. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. D. Nicolas, G. L. Mignon, F. Eber, O. Coriton, H. Monod, V. Clouet, V. Huteau, A. Lostanlen, R. Delourme, B. Chalhoub, et al. Homeologous Recombination Plays a Major Role in Chromosome Rearrangements That Occur During Meiosis of Brassica napus Haploids Genetics, February 1, 2007; 175(2): 487 - 503. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. I. Wright, J. P. Foxe, L. DeRose-Wilson, A. Kawabe, M. Looseley, B. S. Gaut, and D. Charlesworth Testing for Effects of Recombination Rate on Nucleotide Diversity in Natural Populations of Arabidopsis lyrata Genetics, November 1, 2006; 174(3): 1421 - 1430. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kawabe, B. Hansson, J. Hagenblad, A. Forrest, and D. Charlesworth Centromere Locations and Associated Chromosome Rearrangements in Arabidopsis lyrata and A. thaliana Genetics, July 1, 2006; 173(3): 1613 - 1619. [Abstract] [Full Text] [PDF] |
||||