Involvement of rice histone deacetylase HDA705 in seed germination and in response to ABA and abiotic stresses

Histone acetylation and deacetylation play crucial roles in the modification of chromatin structure and regulation of gene expression in eukaryotes. Histone acetyltransferases (HATs) and histone deacetylases (HDACs) assist to maintain the balance of chromatin acetylation status. Previous studies sho...

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Veröffentlicht in:Biochemical and biophysical research communications 2016-02, Vol.470 (2), p.439-444
Hauptverfasser: Zhao, Jinhui, Li, Mingzhi, Gu, Dachuan, Liu, Xuncheng, Zhang, Jianxia, Wu, Kunlin, Zhang, Xinhua, Teixeira da Silva, Jaime A., Duan, Jun
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Sprache:eng
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Zusammenfassung:Histone acetylation and deacetylation play crucial roles in the modification of chromatin structure and regulation of gene expression in eukaryotes. Histone acetyltransferases (HATs) and histone deacetylases (HDACs) assist to maintain the balance of chromatin acetylation status. Previous studies showed that plant HDACs are key regulators involved in response to development and stresses. In this study, we examined the expression pattern and function of HDA705, a member of the RPD3/HDA1-type HDAC in rice. Overexpression of HDA705 in rice decreased ABA and salt stress resistance during seed germination. Delayed seed germination of HDA705 overexpression lines was associated with down-regulated expression of GA biosynthetic genes and up-regulation of ABA biosynthetic genes. Moreover, overexpression of HDA705 in rice enhanced osmotic stress resistance during the seedling stage. Our findings demonstrate that HDA705 may play a role in regulating seed germination and the response to abiotic stresses in rice. •HDA705 is a member of the RPD3/HDA1-type histone deacetylases in rice.•Lower germination rates were detected for HDA705 OX seeds compared to the WT.•Overexpression of HDA705 decreases seed germination under ABA and salt stresses.•Overexpression of HDA705 enhance osmotic resistance during the seedling stage.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2016.01.016