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New Phytol ; 223(4): 1937-1951, 2019 09.
Artigo em Inglês | MEDLINE | ID: mdl-31063599

RESUMO

Accessible chromatin changes dynamically during development and harbours functional regulatory regions which are poorly understood in the context of wood development. We explored the importance of accessible chromatin in Eucalyptus grandis in immature xylem generally, and MYB transcription factor-mediated transcriptional programmes specifically. We identified biologically reproducible DNase I Hypersensitive Sites (DHSs) and assessed their functional significance in immature xylem through their associations with gene expression, epigenomic data and DNA sequence conservation. We identified in vitro DNA binding sites for six secondary cell wall-associated Eucalyptus MYB (EgrMYB) transcription factors using DAP-seq, reconstructed protein-DNA networks of predicted targets based on binding sites within or outside DHSs and assessed biological enrichment of these networks with published datasets. 25 319 identified immature xylem DHSs were associated with increased transcription and significantly enriched for various epigenetic signatures (H3K4me3, H3K27me3, RNA pol II), conserved noncoding sequences and depleted single nucleotide variants. Predicted networks built from EgrMYB binding sites located in accessible chromatin were significantly enriched for systems biology datasets relevant to wood formation, whereas those occurring in inaccessible chromatin were not. Our study demonstrates that DHSs in E. grandis immature xylem, most of which are intergenic, are of functional significance to gene regulation in this tissue.


Assuntos
Cromatina/genética , Eucalyptus/crescimento & desenvolvimento , Madeira/crescimento & desenvolvimento , Sequência de Bases , Biomassa , Parede Celular/metabolismo , Desoxirribonuclease I/metabolismo , Eucalyptus/genética , Redes Reguladoras de Genes , Histonas/metabolismo , Anotação de Sequência Molecular , Fatores de Transcrição/metabolismo , Sítio de Iniciação de Transcrição , Madeira/genética , Xilema/metabolismo
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