Transactivation and transformation by Myb are negatively regulated by a leucine-zipper structure.

Kanei-Ishii, C; MacMillan, E M; Nomura, T; Sarai, A; Ramsay, R G; Aimoto, S; Ishii, S; Gonda, T J · Proc Natl Acad Sci U S A · 1992

basic_science · Level V

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Abstract

The negative regulatory domain of the c-myb protooncogene product (c-Myb) normally represses transcriptional activation by c-Myb. We show here that a leucine-zipper structure is a component of the negative regulatory domain, because its disruption markedly increases both the transactivating and transforming capacities of c-Myb. We also demonstrate that this leucine-zipper structure can interact with cellular proteins. Our results suggest that an inhibitor that suppresses transactivation binds to c-Myb through the leucine zipper and that c-Myb can be oncogenically activated by missense mutation.

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