Interaction between the SH3 domain of Src family kinases and the proline-rich motif of HTLV-1 p13: a novel mechanism underlying delivery of Src family kinases to mitochondria

• Published in: Biochemical journal Vol. 439; no. 3; p. 505
• Main Authors: Tibaldi, Elena, Venerando, Andrea, Zonta, Francesca, Bidoia, Carlo, Magrin, Elisa, Marin, Oriano, Toninello, Antonio, Bordin, Luciana, Martini, Veronica, Pagano, Mario Angelo, Brunati, Anna Maria
• Format: Journal Article
• Language: English
• Published: England 01-11-2011
• Subjects: Amino Acid Motifs; Animals; HeLa Cells; Human T-lymphotropic virus 1 - chemistry; Human T-lymphotropic virus 1 - genetics; Humans; Mitochondrial Proteins - chemistry; Mitochondrial Proteins - genetics; Proline-Rich Protein Domains; Protein Binding; Protein Multimerization - genetics; Protein Transport - genetics; Rabbits; Rats; Retroviridae Proteins - chemistry; Retroviridae Proteins - genetics; src Homology Domains; src-Family Kinases - chemistry; src-Family Kinases - genetics
• ISSN: 1470-8728
• DOI: 10.1042/BJ20101650

The association of the SH3 (Src homology 3) domain of SFKs (Src family kinases) with protein partners bearing proline-rich motifs has been implicated in the regulation of SFK activity, and has been described as a possible mechanism of relocalization of SFKs to subcellular compartments. We demonstrate in the present study for the first time that p13, an accessory protein encoded by the HTLV-1 (human T-cell leukaemia virus type 1), binds the SH3 domain of SFKs via its C-terminal proline-rich motif, forming a stable heterodimer that translocates to mitochondria by virtue of its N-terminal mitochondrial localization signal. As a result, the activity of SFKs is dramatically enhanced, with a subsequent increase in mitochondrial tyrosine phosphorylation, and the recognized ability of p13 to insert itself into the inner mitochondrial membrane and to perturb the mitochondrial membrane potential is abolished. Overall, the present study, in addition to confirming that the catalytic activity of SFKs is modulated by interactors of their SH3 domain, leads us to hypothesize a general mechanism by which proteins bearing a proline-rich motif and a mitochondrial localization signal at the same time may act as carriers of SFKs into mitochondria, thus contributing to the regulation of mitochondrial functions under various pathophysiological conditions.