35
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Nucleotide exchange factor GEF-H1 mediates cross-talk between microtubules and the actin cytoskeleton.

      Nature cell biology
      Actins, metabolism, Animals, COS Cells, DNA, Complementary, Dose-Response Relationship, Drug, Gene Expression Regulation, Genes, Reporter, Guanine Nucleotide Exchange Factors, chemistry, Guanine Nucleotides, HeLa Cells, Humans, Microscopy, Fluorescence, Microtubule-Associated Proteins, Microtubules, Models, Genetic, Plasmids, Precipitin Tests, Protein Structure, Tertiary, Rho Guanine Nucleotide Exchange Factors, Time Factors, Transfection, cdc42 GTP-Binding Protein, rac1 GTP-Binding Protein, ras GTPase-Activating Proteins, ras Guanine Nucleotide Exchange Factors, rhoA GTP-Binding Protein

      Read this article at

      ScienceOpenPublisherPubMed
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Regulation of the actin cytoskeleton by microtubules is mediated by the Rho family GTPases. However, the molecular mechanisms that link microtubule dynamics to Rho GTPases have not, as yet, been identified. Here we show that the Rho guanine nucleotide exchange factor (GEF)-H1 is regulated by an interaction with microtubules. GEF-H1 mutants that are deficient in microtubule binding have higher activity levels than microtubule-bound forms. These mutants also induce Rho-dependent changes in cell morphology and actin organization. Furthermore, drug-induced microtubule depolymerization induces changes in cell morphology and gene expression that are similar to the changes induced by the expression of active forms of GEF-H1. Furthermore, these effects are inhibited by dominant-negative versions of GEF-H1. Thus, GEF-H1 links changes in microtubule integrity to Rho-dependent regulation of the actin cytoskeleton.

          Related collections

          Author and article information

          Comments

          Comment on this article