학술논문

Mixed-lineage kinase 3 regulates B-Raf through maintenance of the B-Raf/Raf-1 complex and. inhibition by the NF2 tumor suppressor protein
CELL BIOLOGY
Document Type
Author abstract
Source
Proceedings of the National Academy of Sciences of the United States. March 21, 2006, Vol. 103 Issue 12, p4463, 6 p.
Subject
Analysis
Structure
Research
Cell proliferation -- Analysis
Mitogens -- Structure
Mitogens -- Research
Neurofibromatosis -- Research
Protein kinases -- Structure
Protein kinases -- Research
Language
English
ISSN
0027-8424
Abstract
The Ras [right arrow] Raf [right arrow] MEK1/2 [right arrow] extracellular signal-regulated kinase (ERK) mitogen-activated protein kinase (MAPK) pathway couples mitogenic signals to cell proliferation. B-Raf and Raf-1 function within an oligomer wherein they are regulated in part by mutual transactivation. The MAPK kinase kinase (MAP3K) mixed-lineage kinase 3 (MLK3) is required for mitogen activation of B-Raf and cell proliferation. Here we show that the kinase activity of MLK3 is not required for support of B-Raf activation. Instead, MLK3 is a component of the B-Raf/Raf-1 complex and is required for maintenance of the integrity of this complex. We show that the activation of ERK and the proliferation of human schwannoma cells bearing a loss-of-function mutation in the neurofibromatosis 2 (NF2) gene require MLK3. We find that merlin, the product of NF2, blunts the activation of both ERK and c-Jun N-terminal kinase (JNK). Finally, we demonstrate that merlin and MLK3 can interact in situ and that merlin can disrupt the interactions between B-Raf and Raf-1 or those between MLK3 and either B-Raf or Raf-1. Thus, MLK3 is part of a multiprotein complex and is required for ERK activation. The levels of this complex may be negatively regulated by merlin. extracellular signal-regulated kinase | mitogen-activated protein kinase/merlin