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MEKK2 inhibits activation of MAP kinases in Arabidopsis.

The Plant journal : for cell and molecular biology (2020-04-09)
Yukino Nitta, Yichun Qiu, Hoda Yaghmaiean, Qian Zhang, Jianhua Huang, Keith Adams, Yuelin Zhang
ABSTRACT

The Arabidopsis MEKK1-MKK1/MKK2-MPK4 kinase cascade is monitored by the nucleotide-binding leucine-rich-repeat immune receptor SUMM2. Disruption of this kinase cascade leads to activation of SUMM2-mediated immune responses. MEKK2, a close paralog of MEKK1, is required for defense responses mediated by SUMM2, the molecular mechanism of which is unclear. In this study, we showed that MEKK2 serves as a negative regulator of MPK4. It binds to MPK4 to directly inhibit its phosphorylation by upstream MKKs. Activation of SUMM2-mediated defense responses induces the expression of MEKK2, which in turn blocks MPK4 phosphorylation to further amplify immune responses mediated by SUMM2. Intriguingly, MEKK2 locates in a tandem repeat consisting of MEKK1, MEKK2 and MEKK3, which was generated from a recent gene duplication event, suggesting that MEKK2 evolved from a MAPKKK to become a negative regulator of MAP kinases.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Anti-AtMPK3 antibody produced in rabbit, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
Anti-AtMPK4 antibody produced in rabbit, affinity isolated antibody, liquid
Sigma-Aldrich
Anti-AtMPK6 antibody produced in rabbit, affinity isolated antibody, liquid