Agriculture Reference
In-Depth Information
of these early phosphorylation events, the evidence reviewed here suggests that
ABA activates a complex network of transcription factors, some of which hav-
ing opposing function in flowering. A more precise understanding of the early
downstream targets of ABA signalling as well as the regulatory logic of the ABA-
related network of transcription factors warrant further investigations.
Recent advancements in hormone signalling reveal how their site of production,
mode of transport and action is strictly controlled; ABA may thus be no exception.
A key goal is therefore to have a better understanding of the spatial context where
ABA acts (perhaps in combination with other hormones) during vegetative devel-
opment. Spatial and temporal constraints might affect the final output of ABA sig-
nalling. Tissue specific and temporal manipulation of ABA signalling could inform
the nature of these constraints. Knowledge obtained through these experiments
will provide concepts that help to understand how enormously variable water-
dependent signals are translated into developmental adaptations in plants.
References
Abe M, et al. FD, a bZIP protein mediating signals from the floral pathway integrator FT at the
shoot apex. Science. 2005;309(5737):1052-6.
Achard P, et al. The plant stress hormone ethylene controls floral transition via DELLA-dependent
regulation of floral meristem-identity genes. Proc Nat Acad Sci USA. 2007;104(15):6484-9.
An H, et al. CONSTANS acts in the phloem to regulate a systemic signal that induces photoperi-
odic flowering of Arabidopsis. Development. 2004;131(15):3615-26.
Balasubramanian S, et al. Potent induction of Arabidopsis thaliana flowering by elevated growth
temperature. PLoS Genet. 2006;2(7):e106.
Barrero JM, et al. A mutational analysis of the ABA1 gene of Arabidopsis thaliana high-
lights the involvement of ABA in vegetative development. Arabidopsis thaliana.
2005;56(418):2071-83.
Bernier G. Physiological signals that induce flowering. Plant Cell. 1993;5(10):1147-55.
Bezerra IC, et al. Lesions in the mRNA cap-binding gene ABA HYPERSENSITIVE 1 sup-
press FRIGIDA-mediated delayed flowering in Arabidopsis. Plant J Cell Mol Biol.
2004;40(1):112-9.
Blanvillain R, et al. Stress tolerance to stress escape in plants: role of the OXS2 zinc-finger tran-
scription factor family. EMBO J. 2011;30(18):3812-22.
Blazquez M, et al. Gibberellins promote flowering of arabidopsis by activating the LEAFY pro-
moter. Plant Cell. 1998;10(5):791-800.
Blázquez MA, et al. A thermosensory pathway controlling flowering time in Arabidopsis thali-
ana. Nat Genet. 2003;33(2):168-71.
Boccalandro HE, et al. Phototropins but not cryptochromes mediate the blue light-specific pro-
motion of stomatal conductance, while both enhance photosynthesis and transpiration under
full sunlight. Plant Physiol. 2012;158(3):1475-84.
Brocard IM, et al. Regulation and role of the Arabidopsis abscisic acid-insensitive 5 gene in
abscisic acid, sugar, and stress response. Plant Physiol. 2002;129(4):1533-43.
Burbidge A, et al. Characterization of the ABA-deficient tomato mutant notabilis and its relation-
ship with maize Vp14 . Plant J. 1999;17(4):427-31.
Busk PK, Pag│s M. Regulation of abscisic acid-induced transcription-Springer. Plant Mol Biol.
1998;37(3):425-35.
Carvalho RF, et al. Convergence of developmental mutants into a single tomato model sys-
tem: “Micro-Tom” as an effective toolkit for plant development research. Plant Methods.
2011;7(1):18.
Search WWH ::




Custom Search