Plant science: FKF1 F-box protein mediates cyclic degradation of a repressor of CONSTANS in Arabidopsis

Science

Volumn 309, Issue 5732, 2005, Pages 293-297

  Imaizumi, Takato ^a   Schultz, Thomas F ^a   Harmon, Frank G ^a   Ho, Lindsey A ^a   Kay, Steve A ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MATERIALS; DEGRADATION; MOLECULAR BIOLOGY; PHOTOREACTIVITY; PROTEINS; REPRESSURING; TRANSCONDUCTANCE;

CYCLIC DEGRADATIONS; PHOTOPERIODIC FLOWERING; TEMPORAL CONTROLS; TRANSCRIPTIONS;

CARBON MONOXIDE;

CDF1 PROTEIN; COMPLEMENTARY DNA; F BOX PROTEIN; FLAVIN BINDING KELCH REPEAT F BOX 1 PROTEIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; ARABIDOPSIS PROTEIN; CDF1 PROTEIN, ARABIDOPSIS; CONSTANS PROTEIN, ARABIDOPSIS; DNA BINDING PROTEIN; FKF1 PROTEIN, ARABIDOPSIS; HYBRID PROTEIN; PROTEASOME; REPRESSOR PROTEIN;

FLOWERING;

ARABIDOPSIS; ARTICLE; DNA BINDING; FLOWERING; GENE EXPRESSION; GENE REPRESSION; GENETIC TRANSCRIPTION; MUTANT; NONHUMAN; PHENOTYPE; PHOTOPERIODICITY; PLANT; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DEGRADATION; AMINO ACID SEQUENCE; BIOSYNTHESIS; CELL NUCLEUS; CHEMISTRY; FLOWER; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; MOLECULAR GENETICS; MUTATION; RNA INTERFERENCE; TRANSGENIC PLANT;

ARABIDOPSIS;

AMINO ACID SEQUENCE; ARABIDOPSIS; ARABIDOPSIS PROTEINS; CELL NUCLEUS; DNA-BINDING PROTEINS; FLOWERS; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, PLANT; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; PLANTS, GENETICALLY MODIFIED; PROTEASOME ENDOPEPTIDASE COMPLEX; RECOMBINANT FUSION PROTEINS; REPRESSOR PROTEINS; RNA INTERFERENCE; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC;

EID: 22044444886     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1110586     Document Type: Article

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19. We thank L. Pettigrew, H. Tran, S. Hazen, and E. Farre for critical reading of the manuscript; M. Yanovsky for involvement in an early stage of this work; K. Hitomi for helping to purify recombinant proteins; K. Spencer for microscopy assistance; P. Waterhouse for pHannibal; C. Barbas III for VP64 plasmid; and the Arabidopsis Biological Resource Center for the transferred DNA insertion line. Supported by an NIH grant (S.A.K.), an NSF Postdoctoral Fellowship in Biosciences Related to the Environment (T.F.S.), and a grant from Japan Society for the Promotion of Science Postdoctoral Fellowships for Research Abroad (T.I.). F.G.H. is a U.S. Department of Energy-Energy Biosciences Research Fellow of the Life Sciences Research Foundation. This is manuscript no. 16849-CB of The Scripps Research Institute.