Clark G J, Drugan J K, Rossman K L, Carpenter J W, Rogers-Graham K, Fu H, Der C J, Campbell S L
Department of Pharmacology, Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
J Biol Chem. 1997 Aug 22;272(34):20990-3. doi: 10.1074/jbc.272.34.20990.
Although Raf-1 is a critical effector of Ras signaling and transformation, the mechanism by which Ras promotes Raf-1 activation is complex and remains poorly understood. We recently reported that Ras interaction with the Raf-1 cysteine-rich domain (Raf-CRD, residues 139-184) may be required for Raf-1 activation. The Raf-CRD is located in the NH2-terminal negative regulatory domain of Raf-1 and is highly homologous to cysteine-rich domains found in protein kinase C family members. Recent studies indicate that the structural integrity of the Raf-CRD is also critical for Raf-1 interaction with 14-3-3 proteins. However, whether 14-3-3 proteins interact directly with the Raf-CRD and how this interaction may mediate Raf-1 function has not been determined. In the present study, we demonstrate that 14-3-3 zeta binds directly to the isolated Raf-CRD. Moreover, mutation of Raf-1 residues 143-145 impairs binding of 14-3-3, but not Ras, to the Raf-CRD. Introduction of mutations that impair 14-3-3 binding resulted in full-length Raf-1 mutants with enhanced transforming activity. Thus, 14-3-3 interaction with the Raf-CRD may serve in negative regulation of Raf-1 function by facilitating dissociation of 14-3-3 from the NH2 terminus of Raf-1 to promote subsequent events necessary for full activation of Raf-1.
尽管Raf-1是Ras信号传导和转化的关键效应器,但Ras促进Raf-1激活的机制很复杂,仍知之甚少。我们最近报道,Ras与Raf-1富含半胱氨酸结构域(Raf-CRD,第139 - 184位氨基酸残基)的相互作用可能是Raf-1激活所必需的。Raf-CRD位于Raf-1的NH2末端负调控结构域中,与蛋白激酶C家族成员中发现的富含半胱氨酸结构域高度同源。最近的研究表明,Raf-CRD的结构完整性对于Raf-1与14-3-3蛋白的相互作用也至关重要。然而,14-3-3蛋白是否直接与Raf-CRD相互作用以及这种相互作用如何介导Raf-1功能尚未确定。在本研究中,我们证明14-3-3ζ直接与分离的Raf-CRD结合。此外,Raf-1第143 - 145位氨基酸残基的突变会损害14-3-3与Raf-CRD的结合,但不影响Ras与Raf-CRD的结合。引入损害14-3-3结合的突变会导致具有增强转化活性的全长Raf-1突变体。因此,14-3-3与Raf-CRD的相互作用可能通过促进14-3-3从Raf-1的NH2末端解离,从而对Raf-1功能起到负调控作用,以促进Raf-1完全激活所需的后续事件。