An atypical HLH protein OsLF in rice regulates flowering time and interacts with OsPIL13 and OsPIL15

New Biotechnology

Volumn 28, Issue 6, 2011, Pages 788-797

  Zhao, Xiao Ling ^a   Shi, Zhen Ying ^a   Peng, Ling Tao ^a   Shen, Ge Zhi ^b   Zhang, Jing Liu ^a  

^a INSTITUTE OF PLANT PHYSIOLOGY AND ECOLOGY   (China)

^b INSTITUTE OF EDIBLE FUNGI   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS; COLOCALIZATION; COLOCALIZE; ENVIRONMENTAL SIGNALS; FLOWERING-TIME; GENE ENCODES; GENETIC ANALYSIS; GENETIC PROGRAMS; LATE-FLOWERING; ORTHOLOGS; OVER-EXPRESSION; PHOTOPERIODIC FLOWERING; REGULATORY PATHWAY; WILD TYPES; YEAST TWO HYBRID;

AMINO ACIDS; PLANTS (BOTANY);

GENES;

PROTEIN OSLF; PROTEIN OSPIL13; PROTEIN OSPIL15; PROTEIN OSPRR1; UNCLASSIFIED DRUG; VEGETABLE PROTEIN;

ARTICLE; DOWN REGULATION; FLOWERING; GENE INSERTION; GENE INTERACTION; GENE ISOLATION; GENE OVEREXPRESSION; NONHUMAN; PHENOTYPE; PLANT GENE; PRIORITY JOURNAL; PROTEIN LOCALIZATION; RICE; SIGNAL TRANSDUCTION; YEAST CELL;

FLOWERS; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; HELIX-TURN-HELIX MOTIFS; ORYZA SATIVA; PHOTOPERIOD; PLANT PROTEINS; TRANSCRIPTION FACTORS;

ARABIDOPSIS;

EID: 80052969475     PISSN: 18716784     EISSN: 18764347     Source Type: Journal    
DOI: 10.1016/j.nbt.2011.04.006     Document Type: Article

References (44)

1. Erisson M.E., et al. Response regulator homologues have complementary, light-dependent functions in the Arabidopsis circadian clock. Planta 2003, 218:159-162.
2. Somers D.E., et al. The short-period mutant, toc1-1, alters circadian clock regulation of multiple outputs throughout development in Arabidopsis thaliana. Development 1998, 125:485-494.
3. Strayer C., et al. Cloning of the Arabidopsis clock gene TOC1, an autoregulatory response regulator homolog. Science 2000, 289:768-771.
4. Makino S., et al. The APRR1/TOC1 quintet implicated in circadian rhythms of Arabidopsis thaliana. I. Characterization with APRR1-overexpressing plants. Plant Cell Physiol. 2002, 43:58-69.
5. Yamashino T., et al. A link between circadian-controlled bHLH factors and the APRR1/TOC1 quintet in Arabidopsis thaliana. Plant Cell Physiol. 2003, 44:619-629.
6. Khanna R., et al. A novel molecular recognition motif necessary for targeting photoactivated phytochrome signaling to specific basic helix-loop-helix transcription factors. Plant Cell 2004, 16:3033-3044.
7. Murakami M., et al. The evolutionarily conserved OsPRR quintet: rice pseudo-response regulators implicated in circadian rhythm. Plant Cell Physiol. 2003, 44:1229-1236.
8. Murakami M., et al. Circadian-associated rice pseudo response regulators (OsPRRs): insight into the control of flowering time. Biosci. Biotechnol. Biochem. 2005, 69:410-414.
9. Nakamura Y., et al. Characterization of a set of phytochrome-interacting factor-like bHLH proteins in Oryza sativa. Biosci. Biotechnol. Biochem. 2007, 71:1183-1191.
10. Simpson G.G., et al. Arabidopsis, the Rosetta stone of flowering time?. Science 2002, 296:285-289.
11. Corbesier L., et al. FT protein movement contributes to long-distance signaling in floral induction of Arabidopsis. Science 2007, 316:1030-1033.
12. Samach A., et al. Distinct roles of CONSTANS target genes in reproductive development of Arabidopsis. Science 2000, 288:1613-1616.
13. Park D.H., et al. Control of circadian rhythms and photoperiodic flowering by the Arabidopsis GIGANTEA gene. Science 1999, 285:1579-1582.
14. Jaeger K.E., et al. FT protein acts as a long-range signal in Arabidopsis. Curr. Biol. 2007, 17:1050-1054.
15. Lin M.K., et al. FLOWERING LOCUS T protein may act as the long-distance florigenic signal in the cucurbits. Plant Cell 2007, 19:1488-1506.
16. Mathieu J., et al. Export of FT protein from phloem companion cells is sufficient for floral induction in Arabidopsis. Curr. Biol. 2007, 17:1055-1060.
17. Hayama R., et al. Adaptation of photoperiodic control pathways produces short-day flowering in rice. Nature 2003, 422:719-722.
18. Kojima S., et al. Hd3a, a rice ortholog of the Arabidopsis FT gene, promotes transition to flowering downstream of Hd1 under short-day conditions. Plant Cell Physiol. 2002, 43:1096-1105.
19. Varshney A., et al. Modulation of voltage sensitivity by N-terminal cytoplasmic residues in human Kv1.2 channels. Eur. Biophys. J. 2002, 31:365-372.
20. Yano M., et al. Hd1, a major photoperiod sensitivity quantitative trait locus in rice, is closely related to the Arabidopsis flowering time gene CONSTANS. Plant Cell 2000, 12:2473-2484.
21. Atchley W.R., et al. A natural classification of the basic helix-loop-helix class of transcription factors. Proc. Natl. Acad. Sci. 1997, 94:5172-5176.
22. Jone S. An overview of the basic helix-loop-helix proteins. Genome Biol. 2004, 5:226.
23. Toledo-Ortiz G., et al. The Arabidopsis basic/helix-loop-helix transcription factor family. Plant Cell 2003, 15:1749-1770.
24. Li X., et al. Genome-wide analysis of basic/helix-loop-helix transcription factor family in rice and Arabidopsis. Plant Physiol. 2006, 141:1167-1184.
25. Wang J., et al. Generation and molecular analysis of a population of transgenic rice plants carrying Ds element. Acta Phytophysiol. Sin. 2000, 26:501-506. (in Chinese).
26. Hiei Y., et al. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J. 1994, 6:271-282.
27. Jain M., et al. Validation of housekeeping genes as internal control for studying gene expression in rice by quantitative real-time PCR. Biochem. Biophys. Res. Commun. 2006, 345:646-651.
28. Takeuchi Y., et al. Plant transformation: a simple particle bombardment device based on flowing helium. Plant Mol. Biol. 1992, 18:835-839.
29. Zhai Z., et al. Establishing RNA interference as a reverse-genetic approach for gene functional analysis in protoplasts. Plant Physiol. 2009, 149:642-652.
30. Zhu Y., et al. Temperature modulates plant defense responses through NB-LRR proteins. PLoS Pathog. 2010, 6:e1000844.
31. Wang J., et al. Distribution of T-DNA carrying a Ds element on rice chromosomes. Sci. China C, Life Sci. 2004, 27:322-331.
32. Chen Z.G., et al. Genetic analysis of a heading-delayed mutant by T-DNA insertion in rice (Oryza sativa L.). Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Bao 2004, 30:75-80.
33. Liu Y.G., et al. Efficient isolation and mapping of Arabidopsis thaliana T-DNA insert junctions by thermal asymmetric interlaced PCR. Plant J. 1995, 8:457-463.
34. Peng L.T., et al. Overexpression of transcription factor OsLFL1 delays flowering time in Oryza sativa. J. Plant Physiol. 2008, 165:876-885.
35. Hyun Y., et al. KIDARI, encoding a non-DNA Binding bHLH protein, represses light signal transduction in Arabidopsis thaliana. Plant Mol. Biol. 2006, 61:283-296.
36. Zhu Y., et al. An interaction between a MYC protein and an EREBP protein is involved in transcriptional regulation of the rice Wx gene. J. Biol. Chem. 2003, 278:47803-47811.
37. Mas P., et al. Dual role of TOC1 in the control of circadian and photomorphogenic responses in Arabidopsis. Plant Cell 2003, 15:223-236.
38. Fairchild C.D., et al. HFR1 encodes an atypical bHLH protein that acts in phytochrome A signal transduction. Genes Dev. 2000, 14:2377-2391.
39. Fankhauser C., et al. RSF1, an Arabidopsis locus implicated in phytochrome A signaling. Plant Physiol. 2000, 124:39-45.
40. Huq E., et al. Phytochrome-interacting factor 1 is a critical bHLH regulator of chlorophyll biosynthesis. Science 2004, 305:1937-1941.
41. Huq E., et al. PIF4, a phytochrome-interacting bHLH factor, functions as a negative regulator of phytochrome B signaling in Arabidopsis. EMBO J. 2002, 21:2441-2450.
42. Oh E., et al. PIL5, a phytochrome-interacting basic helix-loop-helix protein, is a key negative regulator of seed germination in Arabidopsis thaliana. Plant Cell 2004, 16:3045-3058.
43. Salter M.G., et al. Gating of the rapid shade-avoidance response by the circadian clock in plants. Nature 2003, 426:680-683.
44. Soh M.S., et al. REP1, a basic helix-helix protein, is required for a branch pathway of phytochrome A signaling in Arabidopsis. Plant Cell 2000, 12:2061-2074.