Acetylation of the RhoA GEF Net1A controls its subcellular localization and activity.
J Cell Sci
; 128(5): 913-22, 2015 Mar 01.
Article
in En
| MEDLINE
| ID: mdl-25588829
ABSTRACT
Net1 isoform A (Net1A) is a RhoA GEF that is required for cell motility and invasion in multiple cancers. Nuclear localization of Net1A negatively regulates its activity, and we have recently shown that Rac1 stimulates Net1A relocalization to the plasma membrane to promote RhoA activation and cytoskeletal reorganization. However, mechanisms controlling the subcellular localization of Net1A are not well understood. Here, we show that Net1A contains two nuclear localization signal (NLS) sequences within its N-terminus and that residues surrounding the second NLS sequence are acetylated. Treatment of cells with deacetylase inhibitors or expression of active Rac1 promotes Net1A acetylation. Deacetylase inhibition is sufficient for Net1A relocalization outside the nucleus, and replacement of the N-terminal acetylation sites with arginine residues prevents cytoplasmic accumulation of Net1A caused by deacetylase inhibition or EGF stimulation. By contrast, replacement of these sites with glutamine residues is sufficient for Net1A relocalization, RhoA activation and downstream signaling. Moreover, the N-terminal acetylation sites are required for rescue of F-actin accumulation and focal adhesion maturation in Net1 knockout MEFs. These data indicate that Net1A acetylation regulates its subcellular localization to impact on RhoA activity and actin cytoskeletal organization.
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Cytoskeleton
/
Cell Membrane
/
Cell Nucleus
/
Oncogene Proteins
Limits:
Animals
/
Humans
Language:
En
Journal:
J Cell Sci
Year:
2015
Type:
Article
Affiliation country:
United States