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The histone H3 variant H3.3 regulates gene body DNA methylation in Arabidopsis thaliana.

Authors :
Wollmann, Heike
Wollmann, Heike
Stroud, Hume
Yelagandula, Ramesh
Tarutani, Yoshiaki
Jiang, Danhua
Jing, Li
Jamge, Bhagyshree
Takeuchi, Hidenori
Holec, Sarah
Nie, Xin
Kakutani, Tetsuji
Jacobsen, Steven E
Berger, Frédéric
Wollmann, Heike
Wollmann, Heike
Stroud, Hume
Yelagandula, Ramesh
Tarutani, Yoshiaki
Jiang, Danhua
Jing, Li
Jamge, Bhagyshree
Takeuchi, Hidenori
Holec, Sarah
Nie, Xin
Kakutani, Tetsuji
Jacobsen, Steven E
Berger, Frédéric
Source :
Genome biology; vol 18, iss 1, 94; 1474-7596
Publication Year :
2017

Abstract

BackgroundGene bodies of vertebrates and flowering plants are occupied by the histone variant H3.3 and DNA methylation. The origin and significance of these profiles remain largely unknown. DNA methylation and H3.3 enrichment profiles over gene bodies are correlated and both have a similar dependence on gene transcription levels. This suggests a mechanistic link between H3.3 and gene body methylation.ResultsWe engineered an H3.3 knockdown in Arabidopsis thaliana and observed transcription reduction that predominantly affects genes responsive to environmental cues. When H3.3 levels are reduced, gene bodies show a loss of DNA methylation correlated with transcription levels. To study the origin of changes in DNA methylation profiles when H3.3 levels are reduced, we examined genome-wide distributions of several histone H3 marks, H2A.Z, and linker histone H1. We report that in the absence of H3.3, H1 distribution increases in gene bodies in a transcription-dependent manner.ConclusionsWe propose that H3.3 prevents recruitment of H1, inhibiting H1's promotion of chromatin folding that restricts access to DNA methyltransferases responsible for gene body methylation. Thus, gene body methylation is likely shaped by H3.3 dynamics in conjunction with transcriptional activity.

Details

Database :
OAIster
Journal :
Genome biology; vol 18, iss 1, 94; 1474-7596
Notes :
Genome biology vol 18, iss 1, 94 1474-7596
Publication Type :
Electronic Resource
Accession number :
edsoai.on1287322005
Document Type :
Electronic Resource