Specific residues within the alpha 2 integrin subunit cytoplasmic domain regulate migration and cell cycle progression via distinct MAPK pathways.

Klekotka PA, Santoro SA, Wang H, Zutter MM
J Biol Chem. 2001 276 (34): 32353-61

PMID: 11418614 · DOI:10.1074/jbc.M101921200

The alpha(2) integrin subunit cytoplasmic domain is necessary for epidermal growth factor (EGF)-stimulated chemotactic migration and insulin-dependent entry into S-phase of mammary epithelial cells adherent to type I collagen. Truncation mutants revealed that the seven amino acids, KYEKMTK, in addition to the GFFKR motif were sufficient for these functions. Mutation of tyrosine 1134 to alanine inhibited the ability of the cells to phosphorylate p38 MAPK and to migrate in response to EGF but had only a modest effect on the ability of the cells to induce sustained phosphorylation of the ERK MAPK, to up-regulate cyclin E and cdk2 expression, and to enter S-phase when adherent to type I collagen. Conversely, mutation of the lysine 1136 inhibited the ability of the cells to increase cyclin E and cdk2 expression, to maintain long term phosphorylation of the ERK MAPK, and to enter S-phase but had no effect on the ability of the cells to phosphorylate the p38 MAPK or to migrate on type I collagen in response to EGF. Methionine 1137 was essential for both migration and entry into S-phase. Thus, distinctly different structural elements of the alpha(2) integrin cytoplasmic domain are required to engage the signaling pathways leading to cell migration or cell cycle progression.

MeSH Terms (20)

Amino Acid Sequence Animals Antigens, CD CDC2-CDC28 Kinases Cell Cycle Cell Line Cell Movement Cyclin-Dependent Kinase 2 Cyclin-Dependent Kinases Cyclin E Cytoplasm Integrin alpha2 MAP Kinase Signaling System Mice Mitogen-Activated Protein Kinases Molecular Sequence Data p38 Mitogen-Activated Protein Kinases Phenotype Phosphorylation Protein-Serine-Threonine Kinases

Connections (3)

This publication is referenced by other Labnodes entities:

Links