The molecular basis of vernalization: the central role of FLOWERING LOCUS C (FLC).
By C. Sheldon, D. Rouse, E. Finnegan, W. Peacock, E. Dennis. Proceedings of the National Academy of Sciences of the United States of America, 2000
700 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/a946dae3c4c37557bc0f5f128d55cc34e3e8e283
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Citations in the corpus
- The AGAMOUS-LIKE 20 MADS domain protein integrates floral inductive pathways in Arabidopsis. (2000, background): “Late-flowering ecotypes have dominant alleles of FRI and FLC that act synergistically to suppress flowering, whereas early-flowering ecotypes have a recessive allele of FRI and/or weak allele of FLC (Koornneef et al. 1994; Lee et al. 1994b; Sanda and Amasino 1995; Sheldon et al. 2000).”
- No Flower no Fruit - Genetic Potentials to Trigger Flowering in Fruit Trees (2007, background): “On the other hand, FLC is up-regulated by a set of genes, e.g. FRIGIDA (FRI) and VERNALIZATION INDEPENDENCE (VIP) (Michaels and Amasino 1999; Sheldon et al. 2000; Zhang and van Nocker 2002; Zhang et al. 2003).”
- The transcription factor FLC confers a flowering response to vernalization by repressing meristem competence and systemic signaling in Arabidopsis. (2006, background): “In response to vernalization, the abundance of FLC mRNA and protein is reduced (Michaels and Amasino 1999; Sheldon et al. 1999, 2000 ), and therefore vernalization promotes flowering by reducing FLC expression.”
- Gene function beyond the single trait: natural variation, gene effects, and evolutionary ecology in Arabidopsis thaliana (2005, background): “2000) and FLOWERING LOCUS C ( FLC ) (Sheldon et al .”
- Common mechanisms regulate flowering and dormancy (2009, background): “These genes act to repress FLC expression in response to increased temperatures [66].”
- Construct design for efficient, effective and high-throughput gene silencing in plants. (2001, methodology): “To measure the effect of silencing FLC1, 20±30 seeds from each transgenic C24 Arabidopsis line, the transposon mutant ̄c13 (Sheldon et al., 2000), and a control GUS line, were germinated and grown on kanamycin plates as described by Sheldon et al.”
- Naturally occurring genetic variation in Arabidopsis thaliana. (2004, background): “When the functional allelic variation results in gene expression differences, as found for several natural alleles of the FRI andFLC loci (58, 107, 148), this may give a clear indication of which is the candidate gene.”
- Control of flowering time: interacting pathways as a basis for diversity. (2002, background): “Therefore, FLC encodes a repressor of flowering, and highlevel expression of FLC correlates with the vernalization requirement of winter annual varieties (Michaels and Amasino, 1999b; Sheldon et al., 1999, 2000).”
- Potent Induction of Arabidopsis thaliana Flowering by Elevated Growth Temperature (2006, unknown): “Together with its upstream regulator FRI, FLC plays an important role in natural variation of Arabidopsis thaliana flowering [7– 9,11,12,18–21].”
- Reconsidering plant memory: Intersections between stress recovery, RNA turnover, and epigenetics (2016, background): “Significantly, investigations of the FLC loci have demonstrated that memory is mitotically stable (64); memory is quantitative, with the degree of repression of FLC reflecting the length of the cold exposure (65); yet, the epigenetic state of FLC is cell-specific and likely digital, that is, ON/OFF ”
- Multiple Pathways in the Decision to Flower: Enabling, Promoting, and Resetting (2004, background): “Arabidopsis vernalization-responsive mutants and accessions that show a strong vernalization requirement have increased FLC RNA and protein levels, whereas vernalized plants have reduced FLC levels (Sheldon et al., 2000b; Michaels and Amasino, 2001; Rouse et al., 2002).”