The Rac activator STEF (Tiam2) regulates cell migration by microtubule-mediated focal adhesion disassembly.

نویسندگان

  • Claire Rooney
  • Gavin White
  • Alicja Nazgiewicz
  • Simon A Woodcock
  • Kurt I Anderson
  • Christoph Ballestrem
  • Angeliki Malliri
چکیده

Focal adhesion (FA) disassembly required for optimal cell migration is mediated by microtubules (MTs); targeting of FAs by MTs coincides with their disassembly. Regrowth of MTs, induced by removal of the MT destabilizer nocodazole, activates the Rho-like GTPase Rac, concomitant with FA disassembly. Here, we show that the Rac guanine nucleotide exchange factor (GEF) Sif and Tiam1-like exchange factor (STEF) is responsible for Rac activation during MT regrowth. Importantly, STEF is required for multiple targeting of FAs by MTs. As a result, FAs in STEF-knockdown cells have a reduced disassembly rate and are consequently enlarged. This leads to reduced speed of migration. Together, these findings suggest a new role for STEF in FA disassembly and cell migration through MT-mediated mechanisms.

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عنوان ژورنال:
  • EMBO reports

دوره 11 4  شماره 

صفحات  -

تاریخ انتشار 2010