@article {Cummins106971, author = {Timothy D. Cummins and Kevin Z. L. Wu and Polyxeni Bozatzi and Kevin S. Dingwell and Thomas Macartney and Nicola T Wood and Joby Varghese and Robert Gourlay and David G Campbell and Alan Prescott and Eric Griffis and James C Smith and Gopal P Sapkota}, title = {FAM83G/PAWS1 controls cytoskeletal dynamics and cell migration through association with the SH3 adaptor CD2AP}, elocation-id = {106971}, year = {2017}, doi = {10.1101/106971}, publisher = {Cold Spring Harbor Laboratory}, abstract = {Our previous studies of PAWS1 (Protein Associated With SMAD1) have suggested that this molecule has roles beyond BMP signalling. To investigate these roles, we have used CRISPR/Cas9 to generate PAWS1 knockout cells. Here, we show that PAWS1 plays a role in the regulation of the cytoskeletal machinery, including actin and focal adhesion dynamics, and cell migration. Confocal microscopy and live cell imaging of actin in U2OS cells indicate that PAWS1 is also involved in cytoskeletal dynamics and organization. Loss of PAWS1 causes severe defects in F-actin organization and distribution as well as in lamellipodial organization, resulting in impaired cell migration. PAWS1 interacts in a dynamic fashion with the actin/cytoskeletal regulator CD2AP at lamellae, suggesting that its association with CD2AP controls actin organization and cellular migration.Summary statement PAWS1/FAM83G controls cell migration by influencing the organisation of F-actin and focal adhesions and the distribution of the actin stress fibre network through its association with CD2AP.}, URL = {https://www.biorxiv.org/content/early/2017/02/08/106971}, eprint = {https://www.biorxiv.org/content/early/2017/02/08/106971.full.pdf}, journal = {bioRxiv} }