Abstract

The p21-activated kinases are effector proteins for Rho-family GTPases. PAK4, PAK5, and PAK6 are the group II PAKs associated with neurite outgrowth, filopodia formation, and cell survival. Pak4 knockout mice are embryonic lethal, while Pak5, Pak6, and Pak5/Pak6 double knockout mice are viable and fertile. Our previous work found that the double knockout mice exhibit locomotor changes and learning and memory deficits. We also found some differences with Pak5 and Pak6 single knockout mice and the present work further explores the potential differences of the Pak5 knockout and Pak6 knockout mice in comparison with wild type mice. The Pak6 knockout mice were found to weigh significantly more than the other genotypes. The double knockout mice were found to be less active than the other genotypes. The Pak5 knockout mice and the double knockout mice performed worse on the rotorod test. All the knockout genotypes were found to be less aggressive in the resident intruder paradigm. The double knockout mice were, once again, found to perform worse in the active avoidance assay. These results indicate, that although some behavioral differences are seen in the Pak5 and Pak6 single knockout mice, the double knockout mice exhibit the greatest changes in locomotion and learning and memory.

Highlights

  • The p21-activated kinases (PAKs) are effector proteins for the Rho-family GTPases Cdc42 and Rac

  • Animals Pak5 knockout [12], Pak6 knockout and Pak5/Pak6 double knockout (DKO) mice [18] were bred in the Laboratory for Cancer Research, Rutgers University

  • Pak6 knockout mice weigh more than other genotypes An ANOVA was used to analyze the total weight change per genotype from 19 weeks of age to 48 weeks of age

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Summary

Introduction

The p21-activated kinases (PAKs) are effector proteins for the Rho-family GTPases Cdc and Rac. Cdc and Rac are molecular switches involved in several cell processes including cell adhesion and migration as well as apoptosis [1]. There are two families of PAK in mammals; group I which includes PAK1, PAK2, and PAK3, and group II which includes PAK4, PAK5, and PAK6. These families are based on structure and homology. The group II PAKs bind preferentially to Cdc42 Their kinase activity can occur independent of Cdc binding [6]

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