Physical association between Src homology 3 elements and the protein product of the c-cbl proto-oncogene
To investigate the nature of proteins recognized by Src homology 3 (SH3) domains, a cDNA expression library was prepared from macrophages and screened with a probe representing the three SH3 domains of p47nck. Two clones were isolated, and one, designated SAKAP I (for Src A box Nck-associated protei...
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Veröffentlicht in: | The Journal of biological chemistry 1994-07, Vol.269 (26), p.17363-17366 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To investigate the nature of proteins recognized by Src homology 3 (SH3) domains, a cDNA expression library was prepared from
macrophages and screened with a probe representing the three SH3 domains of p47nck. Two clones were isolated, and one, designated
SAKAP I (for Src A box Nck-associated protein I), contained the carboxyl-terminal half of the cbl proto-oncogene product.
Studies in vitro demonstrated reactivity between SAKAP I and SH3 domains derived from a variety of molecules. Wide variations
in this assay suggested a high degree of specificity inherent in SAKAP I binding. Moreover, it was possible to demonstrate
an in vivo association between p47nck and p120c-cbl in HL60 cells. These findings suggest that proteins containing SH3 elements
regulate Cbl function. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/s0021-9258(17)32443-2 |