MAP2K1 Research Reagents

MAP2K1 Background

Dual specificity mitogen-activated protein kinase kinase 1 is a protein in humans that is encoded by the MAP2K1 gene ^[1][2]. MAP2K1 is also called MEK1. Dual specificity protein kinase which acts as an essential component of the MAP kinase signal transduction pathway. Binding of extracellular ligands such as growth factors, cytokines, and hormones to their cell-surface receptors activates RAS and this initiates RAF1 activation. RAF1 further activates the dual-specificity protein kinases MAP2K1/MEK1 and MAP2K2/MEK2. Both MAP2K1/MEK1 and MAP2K2/MEK2 function specifically in the MAPK/ERK cascade, and catalyze the concomitant phosphorylation of a threonine and a tyrosine residue in a Thr-Glu-Tyr sequence located in the extracellular signal-regulated kinases MAPK3/ERK1 and MAPK1/ERK2, leading to their activation and further transduction of the signal within the MAPK/ERK cascade ^[3-7]. The Ras/Raf/Mek/Erk mitogen-activated protein kinase pathway regulates fundamental processes in normal and malignant cells, including proliferation, differentiation, and cell survival, even apoptosis ^[8]. The inactivation of the MEK1 gene leads to embryonic lethality, suggesting an unique role of MEK1 during embryogenesis. Florence A. Scholl et al. demonstrated that disruption of MEK1, but not of MEK2, decreases tumor burden ^[9]. And their study also uncovered that MEK1 function is important for the early stages of skin tumor formation and that MEK2 cannot compensate for its absence ^[9].

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[7] Scholl FA, Dumesic PA, et al. Mek1/2 gene dosage determines tissue response to oncogenic Ras signaling in the skin. Oncogene 2009; 28: 1485-95.
[8] Huynh H, Nguyen TT, et al. Over-expression of the mitogen-activated protein kinase (MAPK) kinase (MEK)-MAPK in hepatocellular carcinoma: its role in tumor progression and apoptosis [J]. BMC Gastroenterol. 2003, Aug 8; 3():19.
[9] Florence A. Scholl, Phillip A. Dumesic, et al. Selective Role for Mek1 but not Mek2 in the Induction of Epidermal Neoplasia [J]. Cell, Tumor, and Stem Cell Biology, Volume 69, Issue 9, pp. 3772-3778.