Cited by 137Protein Kinase Regulation and GTPase SignalingCellular transport and secretionCellular Mechanics and Interactions

XPLN, a guanine nucleotide exchange factor for RhoA and RhoB, but not RhoC

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Arthur, William T., Ellerbroek, Shawn M., Der, Channing J., Burridge, Keith, Wennerberg, Krister·2002·Journal of Biological Chemistry

Abstract

Rho proteins cycle between an inactive, GDP-bound state and an active, GTP-bound state. Activation of these GTPases is mediated by guanine nucleotide exchange factors (GEFs), which promote GDP to GTP exchange. In this study we have characterized XPLN, a Rho family GEF. Like other Rho GEFs, XPLN contains a tandem Dbl homology and pleckstrin homology domain topography, but lacks homology with other known functional domains or motifs. XPLN protein is expressed in the brain, skeletal muscle, heart, kidney, platelets, and macrophage and neuronal cell lines. In vitro, XPLN stimulates guanine nucleotide exchange on RhoA and RhoB, but not RhoC, RhoG, Rac1, or Cdc42. Consistent with these data, XPLN preferentially associates with RhoA and RhoB. The specificity of XPLN for RhoA and RhoB, but not RhoC, is surprising given that they share over 85% sequence identity. We determined that the inability of XPLN to exchange RhoC is mediated by isoleucine 43 in RhoC, a position occupied by valine in RhoA and RhoB. When expressed in cells, XPLN activates RhoA and RhoB, but not RhoC, and stimulates the assembly of stress fibers and focal adhesions in a Rho kinase-dependent manner. We also found that XPLN possesses transforming activity, as determined by focus formation assays. In conclusion, here we describe a Rho family GEF that can discriminate between the closely related RhoA, RhoB, and RhoC, possibly giving insight to the divergent functions of these three proteins.

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  • XPLN shows activity toward RhoA and RhoB but not RhoC due to an amino acid difference (Ile43 vs. Val43) at the N-terminus of the Rho isoforms.

    “One example is XPLN, which shows activity toward RhoA and RhoB but not RhoC due to an amino acid difference (Ile43 vs. Val43) at the N-terminus of the Rho isoforms [20,21].”

    From RhoA Signaling in Neurodegenerative Diseases (2022) · cites this paper as [20]

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Authors
Arthur, W. T., Ellerbroek, S. M., Der, C. J., Burridge, K., & Wennerberg, K.
Affiliations
University of North Carolina at Chapel Hill (US)
Corresponding author
Arthur, William T.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2002-11
Volume
277
Issue
45
Pages
42964-42972
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2065385842
Cited by
137
References
0
Citations by year
2026: 4 · 2025: 5 · 2024: 2 · 2023: 4 · 2022: 9 · 2021: 7 · 2020: 7 · 2019: 1 · 2018: 2 · 2017: 8 · 2016: 7 · 2014: 9 · 2013: 7 · 2012: 7
FWCI
1.95
Type
journal article
Language
en
Open access
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01gm029860-35)
  • National Heart, Lung, and Blood Institute (P01HL045100, HL45100)
  • National Cancer Institute (CA 92240, R01CA063071, R01CA092240, CA63071)
  • National Institute of General Medical Sciences (GM29860)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
Keywords
guanine nucleotide exchange factor, RhoA, RhoB, RhoC, Rho GTPase activation, Dbl homology domain, pleckstrin homology domain, Rho kinase, focal adhesions, oncogenic transformation
MeSH terms
rhoC GTP-Binding Protein, Amino Acid Sequence, Animals, Brain, Cloning, Molecular, HeLa Cells, Humans, Kinetics, Leukemia, Myeloid, Molecular Sequence Data, Organ Specificity, Rabbits, Recombinant Proteins, Substrate Specificity, Transfection, Gene Library, Sequence Alignment, 3T3 Cells, Sequence Homology, Amino Acid, ras Proteins, Guanine Nucleotide Exchange Factors, rho GTP-Binding Proteins, rhoA GTP-Binding Protein, rhoB GTP-Binding Protein, Focal Adhesions, Mice, Rho Guanine Nucleotide Exchange Factors

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