Genetics, Vol. 162, 1457-1468, November 2002, Copyright © 2002

Characterization and Effects of the Replicated Flowering Time Gene FLC in Brassica rapa

M. Eric Schranza, Pablo Quijadaa, Si-Bum Sungb, Lewis Lukensa, Richard Amasinob, and Thomas C. Osborna
a Department of Agronomy, University of Wisconsin, Madison, Wisconsin 53706
b Department of Biochemistry, University of Wisconsin, Madison, Wisconsin 53706

Corresponding author: Thomas C. Osborn, 1575 Linden Dr., University of Wisconsin, Madison, WI 53706., tcosborn{at}facstaff.wisc.edu (E-mail)

Communicating editor: A. PATERSON

Functional genetic redundancy is widespread in plants and could have an important impact on phenotypic diversity if the multiple gene copies act in an additive or dosage-dependent manner. We have cloned four Brassica rapa homologs (BrFLC) of the MADS-box flowering-time regulator FLC, located at the top of chromosome 5 of Arabidopsis thaliana. Relative rate tests revealed no evidence for differential rates of evolution and the ratios of nonsynonymous-to-synonymous substitutions suggest BrFLC loci are not under strong purifying selection. BrFLC1, BrFLC2, and BrFLC3 map to genomic regions that are collinear with the top of At5, consistent with a polyploid origin. BrFLC5 maps near a junction of two collinear regions to Arabidopsis, one of which includes an FLC-like gene (AGL31). However, all BrFLC sequences are more closely related to FLC than to AGL31. BrFLC1, BrFLC2, and BrFLC5 cosegregate with flowering-time loci evaluated in populations derived by backcrossing late-flowering alleles from a biennial parent into an annual parent. Two loci segregating in a single backcross population affected flowering in a completely additive manner. Thus, replicated BrFLC genes appear to have a similar function and interact in an additive manner to modulate flowering time.





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