Integration of Spatial and Temporal Information During Floral Induction in Arabidopsis

By P. Wigge, M. C. Kim, Katja E. Jaeger, Wolfgang Busch, M. Schmid, J. Lohmann, Detlef Weigel. Science, 2005

1,462 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/d1bbaaaf3fd18ec1583cc02458e3ae5669648257

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Citations in the corpus

FT protein acts as a long-range signal in Arabidopsis. (2007, background): “FT protein acts at the shoot apex of the plant in concert with a transcription factor, FLOWERING LOCUS D (FD) [5, 6].”
Reproductive physiology of mango (2007, background): “Once translocated to buds, the protein product of FT is thought to combine with the bZIP transcription factor (FD) protein to activate transcription of floral identity genes, such as APETALA1 (AP1) to begin floral expression (Abe et al., 2005; Wigge et al., 2005).”
The timing of developmental transitions in plants. (2006, background): “Recent comparison of genes activated by shifting wild-type or co mutant plants from noninductive photoperiods into inductive photoperiods showed that only FT activation depends entirely on CO (Wigge et al., 2005).”
miR156-regulated SPL transcription factors define an endogenous flowering pathway in Arabidopsis thaliana. (2009, positive): “Surprisingly, pFD:MIR156 fd -2 plants had a novel inﬂores-cence phenotype, reminiscent of ft lfy , fd lfy , and lfy ap1 double mutants (Figure 4; Abe et al., 2005; Ruiz-Garcı´a et al., 1997; Wigge et al., 2005).”
Global Analysis of DELLA Direct Targets in Early Gibberellin Signaling in Arabidopsis[W] (2007, methodology): “…with Target Promoters in Vivo ChIP is a powerful technique to detect protein–DNA interactions in vivo (Orlando, 2000) and has been used effectively to verify putative direct target genes of transcription factors in Arabidopsis (Wang et al., 2002; Wigge et al., 2005; Levesque et al., 2006).”
CONSTANS and the CCAAT Box Binding Complex Share a Functionally Important Domain and Interact to Regulate Flowering of Arabidopsis[W][OA] (2006, background): “The late-flowering phenotype does not correlate with a reduction in CO mRNA abundance but with a severe decrease in abundance of the mRNA of FT, a gene activated by CO (Samach et al., 2000; Abe et al., 2005; Wigge et al., 2005), suggesting that the basis of the effect of FLAG:At HAP3a is in antagoni”
Cytokinin signaling in plant development (2018, background): “For example, ARR7 and ARR15 are repressed by auxin in the shoot apical meristem (Leibfried et al., 2005; Wigge et al., 2005), but are induced by auxin in the root apical meristem (Müller and Sheen, 2008).”
Genetics of flower initiation and development in annual and perennial plants (2006, positive): “Since FT mRNA appears to be capable of moving from leaves to apex (Abe et al. 2005, Huang et al. 2005, Wigge et al. 2005), it should also be able to move across a graft union in Citrus.”
Role of SVP in the control of flowering time by ambient temperature in Arabidopsis. (2007, background): “2005) and FD (Abe et al. 2005; Wigge et al. 2005) may be also the target of SVP.”
Genomic Survey and Gene Expression Analysis of the Basic Leucine Zipper Transcription Factor Family in Rice1[W][OA] (2007, background): “…in both monocots and dicots have reported the involvement of bZIP transcription factors in transition from the vegetative to the reproductive phase, namely, FD in Arabidopsis (Abe et al., 2005; Wigge et al., 2005) and LIGULELESS2 (LG2) and DELAYED FLOWERING1 (DLF1) in maize (Zea Plant Physiol.”
Regulation and identity of florigen: FLOWERING LOCUS T moves center stage. (2008, background): “Similarly, CaMV 35S promoter–driven overexpression of FT causes ectopic expression of AP1, FUL, and SEP3 in leaves, which is strongly reduced if the transgene is expressed in an fd mutant background (88).”