Quantitative trait locus mapping and DNA array hybridization identify an FLM deletion as a cause for natural flowering-time variation.

Much of the flowering time variation in wild strains of Arabidopsis thaliana is due to allelic variation at two epistatically acting loci, FRIGIDA (FRI) and FLOWERING LOCUS C (FLC). FLC encodes a MADS (MCM1/AGAMOUS/DEFICIENS/SRF1) domain transcription factor that directly represses a series of flowering-promoting genes. FRI and FLC, however, do not explain all of the observed variation, especially when plants are grown in short days. To identify loci that act in addition to FRI and FLC in controlling flowering of natural accessions, we have analyzed a recombinant inbred line population derived from crosses of accession Niederzenz (Nd) to Columbia, both of which contain natural FRI lesions. Quantitative trait locus mapping and genomic DNA analysis by microarray hybridization were used to identify candidate genes affecting variation in flowering behavior. In both long and short days, the quantitative trait locus of largest effect, termed FLOWERING 1 (FLW1), was found to be associated with a Nd-specific deletion of FLOWERING LOCUS M (FLM), which encodes a floral repressor closely related to FLC. Analysis of near isogenic lines and quantitative transgenic complementation experiments confirmed that the FLM deletion is, in large part, responsible for the early flowering of the Nd accession.

[1]  R. Amasino,et al.  siRNAs targeting an intronic transposon in the regulation of natural flowering behavior in Arabidopsis. , 2004, Genes & development.

[2]  M. Purugganan,et al.  Epistatic interaction between Arabidopsis FRI and FLC flowering time genes generates a latitudinal cline in a life history trait. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[3]  S. van Nocker,et al.  A Mechanism Related to the Yeast Transcriptional Regulator Paf1c Is Required for Expression of the Arabidopsis FLC/MAF MADS Box Gene Familyw⃞ , 2004, The Plant Cell Online.

[4]  Sean R. Eddy,et al.  Pack-MULE transposable elements mediate gene evolution in plants , 2004, Nature.

[5]  R. Amasino,et al.  FRIGIDA-related genes are required for the winter-annual habit in Arabidopsis. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[6]  R. Amasino,et al.  Vernalization in Arabidopsis thaliana is mediated by the PHD finger protein VIN3 , 2004, Nature.

[7]  R. Martienssen,et al.  Vernalization requires epigenetic silencing of FLC by histone methylation , 2004, Nature.

[8]  Peter Hajdukiewicz,et al.  The small, versatilepPZP family ofAgrobacterium binary vectors for plant transformation , 1994, Plant Molecular Biology.

[9]  R. Amasino,et al.  Regulation of Flowering Time by Histone Acetylation in Arabidopsis , 2003, Science.

[10]  I. Henderson,et al.  The need for winter in the switch to flowering. , 2003, Annual review of genetics.

[11]  R. Amasino,et al.  Attenuation of FLOWERING LOCUS C activity as a mechanism for the evolution of summer-annual flowering behavior in Arabidopsis , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[12]  C. Lister,et al.  Analysis of the Molecular Basis of Flowering Time Variation in Arabidopsis Accessions1[w] , 2003, Plant Physiology.

[13]  J. Riechmann,et al.  Analysis of the Arabidopsis MADS AFFECTING FLOWERING Gene Family: MAF2 Prevents Vernalization by Short Periods of Cold Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.009506. Online version contains Web-only data. , 2003, The Plant Cell Online.

[14]  Detlef Weigel,et al.  Large-scale identification of single-feature polymorphisms in complex genomes. , 2003, Genome research.

[15]  W. Peacock,et al.  Different Regulatory Regions Are Required for the Vernalization-Induced Repression of FLOWERING LOCUS C and for the Epigenetic Maintenance of Repression Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.004564. , 2002, The Plant Cell Online.

[16]  X. Reboud,et al.  DNA polymorphism at the FRIGIDA gene in Arabidopsis thaliana: extensive nonsynonymous variation is consistent with local selection for flowering time. , 2002, Molecular biology and evolution.

[17]  O. Loudet,et al.  Bay-0 × Shahdara recombinant inbred line population: a powerful tool for the genetic dissection of complex traits in Arabidopsis , 2002, Theoretical and Applied Genetics.

[18]  Detlef Weigel,et al.  Quantitative trait loci controlling light and hormone response in two accessions of Arabidopsis thaliana. , 2002, Genetics.

[19]  A. Peeters,et al.  A QTL for flowering time in Arabidopsis reveals a novel allele of CRY2 , 2001, Nature Genetics.

[20]  J. Riechmann,et al.  Regulation of flowering in Arabidopsis by an FLC homologue. , 2001, Plant physiology.

[21]  R. Amasino,et al.  Identification of a MADS-box gene, FLOWERING LOCUS M, that represses flowering. , 2001, The Plant journal : for cell and molecular biology.

[22]  The Arabidopsis Genome Initiative Analysis of the genome sequence of the flowering plant Arabidopsis thaliana , 2000, Nature.

[23]  R. Amasino,et al.  Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time. , 2000, Science.

[24]  C R Cantor,et al.  Chip-based genotyping by mass spectrometry. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[25]  R. Amasino,et al.  FLOWERING LOCUS C Encodes a Novel MADS Domain Protein That Acts as a Repressor of Flowering , 1999, Plant Cell.

[26]  M. Nordborg,et al.  The effect of seed and rosette cold treatment on germination and flowering time in some Arabidopsis thaliana (Brassicaceae) ecotypes. , 1999, American journal of botany.

[27]  W. Peacock,et al.  The FLF MADS Box Gene: A Repressor of Flowering in Arabidopsis Regulated by Vernalization and Methylation , 1999, Plant Cell.

[28]  L. Liaubet,et al.  Genetic characterization of RRS1, a recessive locus in Arabidopsis thaliana that confers resistance to the bacterial soilborne pathogen Ralstonia solanacearum. , 1998, Molecular plant-microbe interactions : MPMI.

[29]  M Koornneef,et al.  Development of an AFLP based linkage map of Ler, Col and Cvi Arabidopsis thaliana ecotypes and construction of a Ler/Cvi recombinant inbred line population. , 1998, The Plant journal : for cell and molecular biology.

[30]  J. Beynon,et al.  Symbiology of Mouse-Ear Cress (Arabidopsis Thaliana) and Oomycetes , 1997 .

[31]  R. Doerge,et al.  Permutation tests for multiple loci affecting a quantitative character. , 1996, Genetics.

[32]  R. Amasino,et al.  The late-flowering phenotype of FRIGIDA and mutations in LUMINIDEPENDENS is suppressed in the Landsberg erecta strain of Arabidopsis , 1994 .

[33]  M. Koornneef,et al.  The phenotype of some late-flowering mutants is enhanced by a locus on chromosome 5 that is not effective in the Landsberg erecta wild-type , 1994 .

[34]  C. Lister,et al.  Recombinant inbred lines for mapping RFLP and phenotypic markers in Arabidopsis thaliana , 1993 .

[35]  F. Ausubel,et al.  A procedure for mapping Arabidopsis mutations using co-dominant ecotype-specific PCR-based markers. , 1993, The Plant journal : for cell and molecular biology.

[36]  M. Daly,et al.  MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. , 1987, Genomics.