Human CPPED1 belongs to calcineurin‐like metallophosphoesterase superfamily and dephosphorylates PI3K‐AKT pathway component PAK4
| Autor: | Antti M. Haapalainen, Ravindra Daddali, Mika Rämet, Mikko Hallman |
|---|---|
| Přispěvatelé: | Tampere University, Clinical Medicine |
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
0301 basic medicine
Protein family placenta phosphatidylinositide 3‐kinase (PI 3‐kinase) Phosphatase protein‐protein interactions protein-protein interactions AKT1 phosphatase Dephosphorylation 03 medical and health sciences 0302 clinical medicine phosphatidylinositide 3-kinase (PI 3-kinase) Protein kinase B interactomics PI3K/AKT/mTOR pathway CPPED1 Kinase Chemistry AKT PIK3R2 Cell Biology Original Articles Cell biology 030104 developmental biology PAK4 030220 oncology & carcinogenesis Molecular Medicine Phosphorylation Original Article 3111 Biomedicine microarray |
| Zdroj: | Journal of Cellular and Molecular Medicine |
| ISSN: | 1582-4934 1582-1838 |
| Popis: | Protein kinases and phosphatases regulate cellular processes by reversible phosphorylation and dephosphorylation events. CPPED1 is a recently identified serine/threonine protein phosphatase that dephosphorylates AKT1 of the PI3K-AKT signalling pathway. We previously showed that CPPED1 levels are down-regulated in the human placenta during spontaneous term birth. In this study, based on sequence comparisons, we propose that CPPED1 is a member of the class III phosphodiesterase (PDE) subfamily within the calcineurin-like metallophosphoesterase (MPE) superfamily rather than a member of the phosphoprotein phosphatase (PPP) or metal-dependent protein phosphatase (PPM) protein families. We used a human proteome microarray to identify 36 proteins that putatively interact with CPPED1. Of these, GRB2, PAK4 and PIK3R2 are known to regulate the PI3K-AKT pathway. We further confirmed CPPED1 interactions with PAK4 and PIK3R2 by coimmunoprecipitation analyses. We characterized the effect of CPPED1 on phosphorylation of PAK4 and PIK3R2 in vitro by mass spectrometry. CPPED1 dephosphorylated specific serine residues in PAK4, while phosphorylation levels in PIK3R2 remained unchanged. Our findings indicate that CPPED1 may regulate PI3K-AKT pathway activity at multiple levels. Higher CPPED1 levels may inhibit PI3K-AKT pathway maintaining pregnancy. Consequences of decreased CPPED1 expression during labour remain to be elucidated. publishedVersion |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Plný text