Vernalization in Arabidopsis thaliana is mediated by the PHD finger protein VIN3

By Sibum Sung, R. Amasino. Nature, 2004

851 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/0177ba437cf5232dff9673cdaae98a5a0042021a

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

1. R. Amasino
2. M. Schmid
3. G. Coupland
4. Detlef Weigel
5. Anusha Srikanth
6. F. Fornara
7. F. Turck
8. C. Dean

In Plant Science

1. R. Amasino
2. M. Schmid
3. G. Coupland
4. Detlef Weigel
5. Anusha Srikanth
6. F. Fornara
7. F. Turck
8. C. Dean

Citations in the corpus

• Regulation of flowering time: all roads lead to Rome (2011, background): “VIN3 encodes a PHD finger protein and is transiently induced by cold temperatures [96, 97].”
• Multiple Pathways in the Decision to Flower: Enabling, Promoting, and Resetting (2004, background): “These changes in FLC chromatin are dependent on mutations in the vernalization pathway (Bastow et al., 2004; Sung and Amasino, 2004).”
• Seasonal and developmental timing of flowering. (2010, methodology): “…vrn1 mutants, and FLC silencing cannot be maintained after plants return to warm conditions (Levy et al., 2002; Bastow et al., 2004; Flowering-time control 1007 ª 2010 The Author Journal compilation ª 2010 Blackwell Publishing Ltd, The Plant Journal, (2010), 61, 1001–1013 Sung and Amasino, 2004).”
• The transcription factor FLC confers a flowering response to vernalization by repressing meristem competence and systemic signaling in Arabidopsis. (2006, background): “The mechanism of vernalization-mediated epigenetic repression of FLC involves modifications of the histones at FLC chromatin (Gendall et al. 2001; Bastow et al. 2004; Sung and Amasino 2004).”
• 1,135 Genomes Reveal the Global Pattern of Polymorphism in Arabidopsis thaliana (2016, background): “, 2012), not a single SNP reaches genome-wide significance, and the peak might well have been ignored, were it not for the fact that the most significant SNP lies in an intron of the flowering time regulator VIN3 (Sung and Amasino 2004).”
• Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “About 10 ng of RNA was used for quantitative real-time PCR.”
• Seasonal shifts in dormancy status, carbohydrate metabolism, and related gene expression in crown buds of leafy spurge (2005, background): “Induction of flower competency by cold is known to involve chromatin remodelling of specific genes involved in flower development such as FLOW-ERING LOCUS C (Bastow et al. 2004; Sung & Amasino 2004; He & Amasino 2005).”
• DEMETER DNA glycosylase establishes MEDEA polycomb gene self-imprinting by allele-specific demethylation. (2006, background): “Expression of the FLC gene is regulated by vernalization (exposure to cold), which causes an increase in H3K27 dimethylation at the locus (Bastow et al., 2004; Sung and Amasino, 2004).”
• Whole-Genome Analysis of Histone H3 Lysine 27 Trimethylation in Arabidopsis (2007, background): “Red boxes indicated individual genes and arrows indicate direction of transcription [17,19,20,23,33,53,54].”
• Role of SVP in the control of flowering time by ambient temperature in Arabidopsis. (2007, background): “1999) is central to the vernalization process (Sung and Amasino 2005), and this silencing has been attributed to the activities of the VERNALIZATION1 (VRN1), VERNALIZATION2 (VRN2), and VERNALIZATION INSENSITIVE3 (VIN3) genes (Gendall et al. 2001; Levy et al. 2002; Sung and Amasino 2004).”