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  5. An SGS3-like protein functions in RNA-directed DNA methylation and transcriptional gene silencing in Arabidopsis

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Article
en
2010

An SGS3-like protein functions in RNA-directed DNA methylation and transcriptional gene silencing in Arabidopsis

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0 Files

en
2010
Vol 62 (1)
Vol. 62
DOI: 10.1111/j.1365-313x.2010.04130.x

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Jian Kang Zhu
Jian Kang Zhu

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Zhimin Zheng
Yu Xing
Xin‐Jian He
+5 more

Abstract

RNA-directed DNA methylation (RdDM) is an important epigenetic mechanism for silencing transgenes and endogenous repetitive sequences such as transposons. The RD29A promoter-driven LUCIFERASE transgene and its corresponding endogenous RD29A gene are hypermethylated and silenced in the Arabidopsis DNA demethylase mutant ros1. By screening for second-site suppressors of ros1, we identified the RDM12 locus. The rdm12 mutation releases the silencing of the RD29A-LUC transgene and the endogenous RD29A gene by reducing the promoter DNA methylation. The rdm12 mutation also reduces DNA methylation at endogenous RdDM target loci, including transposons and other repetitive sequences. In addition, the rdm12 mutation affects the levels of small interfering RNAs (siRNAs) from some of the RdDM target loci. RDM12 encodes a protein with XS and coiled-coil domains, and is similar to SGS3, which is a partner protein of RDR6 and can bind to double-stranded RNAs with a 5′ overhang, and is required for several post-transcriptional gene silencing pathways. Our results show that RDM12 is a component of the RdDM pathway, and suggest that RdDM may involve double-stranded RNAs with a 5′ overhang and the partnering between RDM12 and RDR2.

How to cite this publication

Zhimin Zheng, Yu Xing, Xin‐Jian He, Wenbo Li, Yuanlei Hu, Sudesh Kumar Yadav, Jee‐Eun Oh, Jian Kang Zhu (2010). An SGS3-like protein functions in RNA-directed DNA methylation and transcriptional gene silencing in Arabidopsis. , 62(1), DOI: https://doi.org/10.1111/j.1365-313x.2010.04130.x.

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Publication Details

Type

Article

Year

2010

Authors

8

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1111/j.1365-313x.2010.04130.x

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