Identification of a C2H2-type zinc finger transcription factor (ZAT10) from Arabidopsis as a substrate of MAP kinase
- Authors
- Xuan Canh Nguyen; Kim, Sun Ho; Lee, Kyunghee; Kim, Kyung Eun; Liu, Xiao-Min; Hay Ju Han; My Hanh Thi Hoang; Lee, Shin-Woo; Hong, Jong Chan; Moon, Yong-Hwan; Chung, Woo Sik
- Issue Date
- Apr-2012
- Publisher
- SPRINGER
- Keywords
- Arabidopsis; C2H2-type zinc finger; MPK; Phosphorylation; Substrate; ZAT10
- Citation
- PLANT CELL REPORTS, v.31, no.4, pp 737 - 745
- Pages
- 9
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- PLANT CELL REPORTS
- Volume
- 31
- Number
- 4
- Start Page
- 737
- End Page
- 745
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/22245
- DOI
- 10.1007/s00299-011-1192-x
- ISSN
- 0721-7714
1432-203X
- Abstract
- Mitogen-activated protein kinases (MAPKs or MPKs) are one of the most important and conserved signaling molecules in plants. MPKs can directly modulate gene expression by the phosphorylation of transcription factors. However, only a few target substrates of MPKs have been isolated. Here, we identified a C2H2-type zinc finger transcription factor from Arabidopsis, ZAT10, as a substrate of MPKs. Using in vitro and in vivo protein-protein interaction analyses, we demonstrated that ZAT10 directly interacted with MPK3 and MPK6. ZAT10 was phosphorylated by recombinant Arabidopsis MPK3 and MPK6 in a kinase assay. Furthermore, ZAT10 was also phosphorylated by native MPK3 and MPK6 prepared from Arabidopsis plants in an in-gel kinase assay. Mass spectrometry analysis of phosphopeptides was used to determine two MPK phosphorylation sites in ZAT10. These sites were verified by site-directed mutagenesis and in vitro kinase assays.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - ETC > Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.