Expanding functions of GIT Arf GTPase-activating proteins, PIX Rho guanine nucleotide exchange factors and GIT–PIX complexes

Author:

Zhou Wu1,Li Xiaobo2,Premont Richard T.3

Affiliation:

1. Department of Medicine, College of Medicine and Health, Lishui University, Lishui 323000, China

2. Department of Computer Science and Technology, College of Engineering and Design, Lishui University, Lishui 323000, China

3. Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA

Abstract

ABSTRACT The GIT proteins, GIT1 and GIT2, are GTPase-activating proteins (inactivators) for the ADP-ribosylation factor (Arf) small GTP-binding proteins, and function to limit the activity of Arf proteins. The PIX proteins, α-PIX and β-PIX (also known as ARHGEF6 and ARHGEF7, respectively), are guanine nucleotide exchange factors (activators) for the Rho family small GTP-binding protein family members Rac1 and Cdc42. Through their multi-domain structures, GIT and PIX proteins can also function as signaling scaffolds by binding to numerous protein partners. Importantly, the constitutive association of GIT and PIX proteins into oligomeric GIT–PIX complexes allows these two proteins to function together as subunits of a larger structure that coordinates two distinct small GTP-binding protein pathways and serves as multivalent scaffold for the partners of both constituent subunits. Studies have revealed the involvement of GIT and PIX proteins, and of the GIT–PIX complex, in numerous fundamental cellular processes through a wide variety of mechanisms, pathways and signaling partners. In this Commentary, we discuss recent findings in key physiological systems that exemplify current understanding of the function of this important regulatory complex. Further, we draw attention to gaps in crucial information that remain to be filled to allow a better understanding of the many roles of the GIT–PIX complex in health and disease.

Funder

zhejiang province natural science funding

National Natural Science Funds of China

National Institutes of Health

DOD

Publisher

The Company of Biologists

Subject

Cell Biology

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