1. Academic Validation
  2. The helicase, DDX3X, interacts with poly(A)-binding protein 1 (PABP1) and caprin-1 at the leading edge of migrating fibroblasts and is required for efficient cell spreading

The helicase, DDX3X, interacts with poly(A)-binding protein 1 (PABP1) and caprin-1 at the leading edge of migrating fibroblasts and is required for efficient cell spreading

  • Biochem J. 2017 Aug 30;474(18):3109-3120. doi: 10.1042/BCJ20170354.
Alice C Copsey 1 Simon Cooper 1 Robert Parker 2 Ella Lineham 1 Cuzack Lapworth 1 Deema Jallad 1 Steve Sweet 3 Simon J Morley 4
Affiliations

Affiliations

  • 1 Department of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K.
  • 2 Faculty of Medicine, National Heart & Lung Institute, St Mary's Campus, Imperial College London, London W2 1NY, U.K.
  • 3 Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN1 9RQ, U.K.
  • 4 Department of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K. s.j.morley@sussex.ac.uk.
Abstract

DDX3X, a helicase, can interact directly with mRNA and translation initiation factors, regulating the selective translation of mRNAs that contain a structured 5' untranslated region. This activity modulates the expression of mRNAs controlling cell cycle progression and mRNAs regulating actin dynamics, contributing to cell adhesion and motility. Previously, we have shown that ribosomes and translation initiation factors localise to the leading edge of migrating fibroblasts in loci enriched with actively translating ribosomes, thereby promoting steady-state levels of ArpC2 and Rac1 proteins at the leading edge of cells during spreading. As DDX3X can regulate Rac1 levels, cell motility and metastasis, we have examined DDX3X protein interactions and localisation using many complementary approaches. We now show that DDX3X can physically interact and co-localise with poly(A)-binding protein 1 and caprin-1 at the leading edge of spreading cells. Furthermore, as depletion of DDX3X leads to decreased cell motility, this provides a functional link between DDX3X, caprin-1 and initiation factors at the leading edge of migrating cells to promote cell migration and spreading.

Keywords

DDX3X; cell migration; translation; translation factors.

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