References
- Albani, D. and Robert, L. S. (1995) Cloning and characterization of a Brassica napus gene encoding a homologue of the Bsubunit of a heteromeric CCAAT-binding factor. Gene 167, 209-213. https://doi.org/10.1016/0378-1119(95)00680-X
- Bucher P., (1990) Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated prolaboratory. J. Mol. Biol. 212, 563-578. https://doi.org/10.1016/0022-2836(90)90223-9
- Cao, S. Q., Ye, M. and Jiang, S. T. (2005) Involvement of GIGANTEA gene in the regulation of the cold stress response in Arabidopsis. Plant Cell Rep. 24, 683-690. https://doi.org/10.1007/s00299-005-0061-x
- Chai, M. F., Wei, P. C., Chen, Q. J., An, R., Chen, J., Yang, S. and Wang, X. C. (2006) NADK3, a novel cytoplasmic source of NADPH, is required under conditions of oxidative stress and modulates abscisic acid responses in Arabidopsis. Plant J. 47, 665-674. https://doi.org/10.1111/j.1365-313X.2006.02816.x
- Combier, J. P., Frugier, F., de Billy, F., A. Boualem, El-Yahyaoui, F., Moreau, S., Vernie, T., Ott, T., Gamas, P., Crespi, M. and Niebel, A. (2006) MtHAP2-1 is a key transcriptional regulator of symbiotic nodule development regulated by microRNA169 in Medicago truncatula. Genes Dev. 20, 3084-3088. https://doi.org/10.1101/gad.402806
- Edwards, D., Murrey, J. A. H. and Smith, A. G., (1998) Multiple genes coding the conserved CCAAT-box transcription complex are expressed in Arabidopsis. Plant Physiol. 117, 1015-1022. https://doi.org/10.1104/pp.117.3.1015
- Forsburg, S. L. and Guarente, L., (1989) Identification and characterization of HAP4: a third component of CCAATbinding HAP2/HAP3 heteromer. Genes Dev. 3, 1166-1178. https://doi.org/10.1101/gad.3.8.1166
- Gusmaroli, G., Tonelli, C., and Mantovani, R. (2002) Regulation of novel members of the Arabidopsis thaliana CCAAT-binding nuclearfactor Y subunits. Gene 283, 41-48. https://doi.org/10.1016/S0378-1119(01)00833-2
- Gusmaroli, G., Tonelli, C. and Mantovani, R., (2001) Regulation of the CCAAT-binding NF-Y subunits in Arabidopsis thaliana. Gene 264, 173-185. https://doi.org/10.1016/S0378-1119(01)00323-7
- Kim, H. J., Hyun, Y., Park, J. Y., Park, M. J., Park, M. Y., Kim, M. D., Kim, H. J., Lee, M. H., Moon, J., Lee, I. and Kim J. (2004) A genetic link between cold responses and flowering time through FVE in Arabidopsis thaliana. Nat. Genet. 36, 167-171. https://doi.org/10.1038/ng1298
- Koornneef, M., Alonso-Blanco, C., Blankestijn-de Vries, H., Hanhart, C. and Peeters, A. (1998) Genetic interactions among late-flowering mutants of Arabidopsis. Genetics 148, 885-892.
- Kwong, R. W., Bui, A. Q., Lee, H., Kwong, L. W., Fischer, R. L., Goldberg, R. B. and Harada, J. J. (2003) LEAFY COTYLEDON1-LIKE defines a class of regulators essential for embryo development. Plant Cell 15, 5-18. https://doi.org/10.1105/tpc.006973
- Lee, H. S., Fischer, R. L., Goldberg, R. B. and Harada, J. J. (2003) Arabidopsis LEAFY COTYLEDON1 represents a functionally specializedsubunit of the CCAAT binding transcription factor. Proc. Natl. Acad. Sci. USA 100, 2152-2156. https://doi.org/10.1073/pnas.0437909100
- Li, X. Y., Mantovani, R., Vanhuijsduijnen, R. H., Andre, I., Benoist, C. and Mathis, D. (1992) Evolutionary variation of the CCAAT-binding transcription factor NF-Y. Nucleic Acids Res. 20, 1087-1091. https://doi.org/10.1093/nar/20.5.1087
- Lotan, T., Ohto, M., Yee, K. M., West, M. A., Lo, R., Kwong, R. W., Yamagishi, K., Fischer, R. L., Goldberg, R. B. and Harada, J. J. (1998) Arabidopsis LEAFY COTYLEDON1 is sufficient to induce embryo development in vegetative cells. Cell 93, 1195-1205. https://doi.org/10.1016/S0092-8674(00)81463-4
- Maity, S. and de Crombrugghe, B. (1998) Role of the CCAATbinding protein CBF/NF-Y in transcription. Trends Biochem. Sci. 23, 174-178. https://doi.org/10.1016/S0968-0004(98)01201-8
- Mantovani, R. (1999) The molecular biology of the CCAATbinding factor NF-Y. Gene 239, 15-27. https://doi.org/10.1016/S0378-1119(99)00368-6
- McNabb, D. S., Tseng, K. A. and Guarente, L. (1997) The Saccaromyces cerevisiae Hap5p homologue from fission yeast reveals two conserved domains that are essential for assembly of heterotetrameric CCAAT binding factor. Mol. Cell. Biol. 17, 7008-7018. https://doi.org/10.1128/MCB.17.12.7008
- Miyoshi, K., Ito, Y., Serizawa, A. and Kurata, N. (2003) OsHAP3 genes regulate chloroplast biogenesis in rice. Plant J. 36, 532-540. https://doi.org/10.1046/j.1365-313X.2003.01897.x
- Robson, F., Costa, M. M. R., Hepworth, S. R., Vizir, I., Pineiro, M., Reeves, P. H., Putterill, J. and Coupland, G. (2001) Functional importance of conserved domains in the floweringtime gene CONSTANS demonstrated by analysis of mutant alleles and transgenic plants. Plant J. 28, 619-631. https://doi.org/10.1046/j.1365-313x.2001.01163.x
- Romier, C., Cocchiarella, F., Mantovani, R. and Moras, D. (2003) The NF-YB/NF-YC structure gives insight into DNA binding and transcription regulation by CCAAT factor NF-Y. J. Biol. Chem. 278, 1336-1345. https://doi.org/10.1074/jbc.M209635200
- Ruiz-Garcia, L., Madueno, F., Wilkinson, M., Haughn, G., Salinas, J. and Martinez-Zapater, J., Wenkel, S., Turck, F., Singer, K., Gissot, L., Le Gourrierec, J., Samach, A. and Coupland, G. (2006) CONSTANS and the CCAAT box Binding complex share a functionally important domain and interact to regulate flowering of Arabidopsis. Plant Cell 18, 2971-2984. https://doi.org/10.1105/tpc.106.043299
- Wigge, P. A., Kim, M. C., Jaeger, K. E., Busch, W., Schmid, M., Lohmann, J. U. and Weigel, D. (2005) Integration of spatial and temporal information during floral induction in Arabidopsis. Science 309, 1056-1059. https://doi.org/10.1126/science.1114358
- Xing, Y. Y., Zhang, S. U., Olesen, J. T., Rich, A. and Guarente, L. (1994) Subunit interaction in the CCAAT-binding heteromeric complex is mediated by a very short alpha-helix in HAP2. Proc. Natl. Acad. Sci. USA 91, 3009-3013. https://doi.org/10.1073/pnas.91.8.3009
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