[1]Chen M, Chory J, Fankhauser C. Light signal transduction in higher plants. Annual Review of Genetics, 2004, 38: 87-117.[2]Yanovsky M J, Izaguirre M, Wagmaister J A, Gatz C, Jackson S D, Thomas B, Casal J J. Phytochrome A resets the circadian clock and delays tuber formation under long days in potato. The Plant Journal, 2000, 23: 223-232.[3]Jackson S, Heyer A, Dietze J, Prat S. Phytochrome B mediates the photoperiodic control of tuber formation in potato. The Plant Journal, 1996, 9: 159-166.[4]Jackson S D, James P, Prat S, Thomas B. Phytochrome B affects the levels of a graft-transmissible signal involved in tuberization. Plant Physiology, 1998, 117: 29-32.[5]Strasser B, Sanchez-Lamas M, Yanovsky M J, Casal J J, Cerdan P D. Arabidopsis thaliana life without phytochromes. Proceedings of the National Acadamy of Science of the USA, 2010, 107: 4776-4781.[6]Suetsugu N, Wada M. Evolution of three LOV blue light receptor families in green plants and photosynthetic stramenopiles: Phototropin, ZTL/FKF1/LKP2 and aureochrome. Plant Cell Physiology, 2013, 54: 8-23.[7]Inui H, Ogura Y, Kiyosue T. Overexpression of Arabidopsis thaliana LOV KELCH REPEAT PROTEIN 2 promotes tuberization in potato (Solanum tuberosum cv. May Queen). FEBS Letters, 2010, 584: 2393-2396.[8]Kloosterman B, Abelenda J A, Gomez Mdel M, Oortwijn M, de Boer J M, Kowitwanich K, Horvath B M, van Eck H J, Smaczniak C, Prat S, Visser R G F, Bachem C W B. Naturally occurring allele diversity allows potato cultivation in northern latitudes. Nature, 2013, 495: 246-250.[9]Kinmonth-Schultz H A, Golembeski G S, Imaizumi T. Circadian clock-regulated physiological outputs: Dynamic responses in nature. Seminars in Cell & Developmental Biology, 2013, 24: 407-413.[10]McClung C R, Salome P A, Michael T P. The Arabidopsis circadian system. Arabidopsis Book, 2002, 1: e0044.[11]Rutitzky M, Ghiglione H O, Cura J A, Casal J J, Yanovsky M J. Comparative genomic analysis of light-regulated transcripts in the Solanaceae. BMC Genomics, 2009, 10: 60.[12]Song Y H, Smith R W, To B J, Millar A J, Imaizumi T. FKF1 conveys timing information for CONSTANS stabilization in photoperiodic flowering. Science, 2012, 336: 1045-1049.[13]Sawa M, Nusinow D A, Kay S A, Imaizumi T. FKF1 and GIGANTEA complex formation is required for day-length measurement in Arabidopsis. Science, 2007, 318: 261-265.[14]Cerdan P D, Chory J. Regulation of flowering time by light quality. Nature, 2003, 423: 881-885.[15]Roden L C, Song H R, Jackson S, Morris K, Carre I A. Floral responses to photoperiod are correlated with the timing of rhythmic expression relative to dawn and dusk in Arabidopsis. Proceedings of the National Academy of Science of the USA, 2002, 99: 13313-13318.[16]Suarez-Lopez P, Wheatley K, Robson F, Onouchi H, Valverde F, Coupland G. CONSTANS mediates between the circadian clock and the control of flowering in Arabidopsis. Nature, 2001, 410: 1116-1120.[17]Valverde F, Mouradov A, Soppe W, Ravenscroft D, Samach A, Coupland G. Photoreceptor regulation of CONSTANS protein in photoperiodic flowering. Science, 2004, 303: 1003-1006.[18]Martinez-Garcia J F, Virgos-Soler A, Prat S. Control of photoperiod- regulated tuberization in potato by the Arabidopsis flowering-time gene CONSTANS. Proceedings of the National Acadamy of Science of the USA, 2002, 99: 15211-15216.[19]Gonzalez-Schain N D, Suarez-Lopez P. CONSTANS delays flowering and affects tuber yield in potato. Biologia Plantarum, 2008, 52: 251-258.[20]Gonzalez-Schain N D, Diaz-Mendoza M, Zurczak M, Suarez-Lopez P. Potato CONSTANS is involved in photoperiodic tuberization in a graft-transmissible manner. The Plant Journal, 2012, 70: 678-690.[21]Kardailsky I, Shukla V K, Ahn J H, Dagenais N, Christensen S K, Nguyen J T, Chory J, Harrison M J, Weigel D. Activation tagging of the floral inducer FT. Science, 1999, 286: 1962-1965.[22]An H, Roussot C, Suarez-Lopez P, Corbesier L, Vincent C, Pineiro M, Hepworth S, Mouradov A, Justin S, Turnbull C, Coupland G. CONSTANS acts in the phloem to regulate a systemic signal that induces photoperiodic flowering of Arabidopsis. Development, 2004, 131: 3615-3626.[23]Corbesier L, Vincent C, Jang S, Fornara F, Fan Q, Searle I, Giakountis A, Farrona S, Gissot L, Turnbull C, Coupland G. FT protein movement contributes to long-distance signaling in floral induction of Arabidopsis. Science, 2007, 316: 1030-1033.[24]Chailakyan M, Yanina L, Devedzhyan A, Lotova G. Photoperiodism and tuber formation in grafting of tobacco on to potato. Doklady Akademii Nauk SSSR, 1981, 257: 1276-1279.[25]Navarro C, Abelenda J A, Cruz-Oro E, Cuellar C A, Tamaki S, Silva J, Shimamoto K, Prat S. Control of flowering and storage organ formation in potato by FLOWERING LOCUS T. Nature, 2011, 478: 119-122.[26]Lin T, Sharma P, Gonzalez D H, Viola I L, Hannapel D J. The impact of the long-distance transport of a BEL1-like messenger RNA on development. Plant Physiology, 2013, 161: 760-772.[27]Mahajan A, Bhogale S, Kang I H, Hannapel D J, Banerjee A K. The mRNA of a Knotted1-like transcription factor of potato is phloem mobile. Plant Molecular Biology, 2012, 79: 595-608.[28]Martin A, Adam H, Diaz-Mendoza M, Zurczak M, Gonzalez-Schain N D, Suarez-Lopez P. Graft-transmissible induction of potato tuberization by the microRNA miR172. Development, 2009, 136: 2873-2881.[29]Chatterjee M, Banerjee A K, Hannapel D J. A BELL1-like gene of potato is light activated and wound inducible. Plant Physiology, 2007, 145: 1435-1443.[30]Banerjee A K, Chatterjee M, Yu Y, Suh S G, Miller W A, Hannapel D J. Dynamics of a mobile RNA of potato involved in a long-distance signaling pathway. The Plant Cell, 2006, 18: 3443-3457.[31]Chen H, Banerjee A K, Hannapel D J. The tandem complex of BEL and KNOX partners is required for transcriptional repression of ga20ox1. The Plant Journal, 2004, 38: 276-284.[32]Rosin F M, Hart J K, Horner H T, Davies P J, Hannapel D J. Overexpression of a knotted-like homeobox gene of potato alters vegetative development by decreasing gibberellin accumulation. Plant Physiology, 2003, 132: 106-117.[33]Chen H, Rosin F M, Prat S, Hannapel D J. Interacting transcription factors from the three-amino acid loop extension superclass regulate tuber formation. Plant Physiology, 2003, 132: 1391-1404.[34]Abe M, Kobayashi Y, Yamamoto S, Daimon Y, Yamaguchi A, Ikeda Y, Ichinoki H, Notaguchi M, Goto K, Araki T. FD, a bZIP protein mediating signals from the floral pathway integrator FT at the shoot apex. Science, 2005, 309: 1052-1056.[35]Wigge P A, Kim M C, Jaeger K E, Busch W, Schmid M, Lohmann J U, Weigel D. Integration of spatial and temporal information during floral induction in Arabidopsis. Science, 2005, 309: 1056-1059.[36]Yamaguchi S. Gibberellin metabolism and its regulation. Annual Review of Plant Biology, 2008, 59: 225-251.[37]Abelenda J A, Navarro C, Prat S. From the model to the crop: Genes controlling tuber formation in potato. Current Opinion in Biotechnology, 2011, 22: 287-292. |