Prevention of early flowering by expression of FLOWERING LOCUS C requires methylation of histone H3

Author:  ["Zhong Zhao","Yu Yu","Denise Meyer","Chengjun Wu","Wen-Hui Shen"]

Publication:  Nature Cell Biology

CITE.CC academic search helps you expand the influence of your papers.

Tags:  general   CellBiology   CancerResearch   DevelopmentalBiology   StemCells   Biological

Abstract

Flowering represents a crucial transition from a vegetative to a reproductive phase of the plant life cycle. Despite extensive studies, the molecular mechanisms controlling flowering remain elusive. Although the enzymes involved are unknown, methylation of histone H3 K9 and K27 correlates with repression of FLOWERING LOCUS C (FLC), an essential transcriptional repressor involved in flowering time control in Arabidopsis thaliana; in contrast, methylation of H3K4 correlates with FLC activation1,2,3,4. Here we show that loss-of-function of SET DOMAIN GROUP 8 (SDG 8), which encodes a homologue of the yeast SET2 histone methyltransferase, results in reduced dimethylation of histone H3K36, particularly in chromatin associated with the FLC promoter and the first intron, regions that contain essential cis-elements for transcription. sdg8 mutants display reduced FLC expression and flower early, establishing SDG8-mediated H3K36 methylation as a novel epigenetic memory code required for FLC expression in preventing early flowering. This is the first demonstrated role of H3K36 methylation in eukaryote development.

Cite this article

Zhao, Z., Yu, Y., Meyer, D. et al. Prevention of early flowering by expression of FLOWERING LOCUS C requires methylation of histone H3 K36. Nat Cell Biol 7, 1256–1260 (2005). https://doi.org/10.1038/ncb1329

View full text

>> Full Text:   Prevention of early flowering by expression of FLOWERING LOCUS C requires methylation of histone H3

Polycystin-1 and polycystin-2 regulate the cell cycle through the helix–loop–helix inhibitor Id2

Loading history determines the velocity of actin-network growth