# Phospho‐Proteomics Identifies D‐Group MAP Kinases as Substrates of the Arabidopsis Tyrosine Phosphatase RLPH2

## TL;DR

This study uses phospho-proteomics to discover that a plant tyrosine phosphatase, RLPH2, targets specific mitogen-activated protein kinases (MPKs) in Arabidopsis, revealing new insights into plant signaling.

## Contribution

The study identifies D-group MPKs as substrates of RLPH2 and reveals a unique PP1 binding motif specific to these MPKs.

## Key findings

- RLPH2 preferentially dephosphorylates D-group MPKs with a TDY activation loop motif.
- D-group MPKs have a unique PP1 binding motif absent in other MPK groups.
- RLPH2-deficient plants show reduced repression of seed dormancy release.

## Abstract

Despite being one of the few bona fide plant tyrosine phosphatases, the
Arabidopsis thaliana

Rhizobiales‐like phosphatase 2 (RLPH2) has no known substrates. Utilizing phospho‐proteomics, we identified the activation loop phospho‐tyrosine of several
A. thaliana
D‐group mitogen‐activated protein kinases (MPKs) as potential RLPH2 substrates. All Arabidopsis D‐group MPKs possess a TDY activation loop phosphorylation motif, whereas other MPKs (Groups A, B, and C) contain a TEY motif. Our findings reveal that RLPH2 has a strong preference for aspartate (D) in the TXY motif, providing specificity for RLPH2 to exclusively target and dephosphorylate the D‐group MPKs. Additionally, D‐group MPKs contain a unique activation loop insertion that conforms to a protein phosphatase one (PP1) binding motif, with findings presented here confirming Arabidopsis PP1 phosphatases dock at this site. Intriguingly, only D‐group MPKs among all identified Arabidopsis protein kinases possess this PP1 recruiting motif. Using multiple RLPH2‐deficient plant lines, we demonstrate that RLPH2 represses seed dormancy release. Overall, this work highlights the power of phospho‐proteomics in identifying substrates of this novel plant tyrosine phosphatase while also revealing new complexities in the interactions between MPK activation loops and multiple phospho‐mediated cell signaling events.