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  5. The chromatin remodeler DDM1 promotes hybrid vigor by regulating salicylic acid metabolism

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Article
en
2016

The chromatin remodeler DDM1 promotes hybrid vigor by regulating salicylic acid metabolism

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en
2016
Vol 2 (1)
Vol. 2
DOI: 10.1038/celldisc.2016.27

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Jian Kang Zhu
Jian Kang Zhu

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Qingzhu Zhang
Yanqiang Li
Tao Xu
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Abstract

In plants, hybrid vigor is influenced by genetic and epigenetic mechanisms; however, the molecular pathways are poorly understood. We investigated the potential contributions of epigenetic regulators to heterosis in Arabidposis and found that the chromatin remodeler DECREASED DNA METHYLATION 1 (DDM1) affects early seedling growth heterosis in Col/C24 hybrids. ddm1 mutants showed impaired heterosis and increased expression of non-additively expressed genes related to salicylic acid metabolism. Interestingly, our data suggest that salicylic acid is a hormetic regulator of seedling growth heterosis, and that hybrid vigor arises from crosses that produce optimal salicylic acid levels. Although DNA methylation failed to correlate with differential non-additively expressed gene expression, we uncovered DDM1 as an epigenetic link between salicylic acid metabolism and heterosis, and propose that the endogenous salicylic acid levels of parental plants can be used to predict the heterotic outcome. Salicylic acid protects plants from pathogens and abiotic stress. Thus, our findings suggest that stress-induced hormesis, which has been associated with increased longevity in other organisms, may underlie specific hybrid vigor traits.

How to cite this publication

Qingzhu Zhang, Yanqiang Li, Tao Xu, Ashish Kumar Srivastava, Dong Wang, Liang Zeng, Lan Yang, Li He, Heng Zhang, Zhimin Zheng, Dong‐Lei Yang, Cheng Zhao, Juan Dong, Zhizhong Gong, Renyi Liu, Jian Kang Zhu (2016). The chromatin remodeler DDM1 promotes hybrid vigor by regulating salicylic acid metabolism. , 2(1), DOI: https://doi.org/10.1038/celldisc.2016.27.

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Publication Details

Type

Article

Year

2016

Authors

16

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1038/celldisc.2016.27

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