A constitutively active and nuclear form of the MAP kinase ERK2 is sufficient for neurite outgrowth and cell transformation - PubMed (original) (raw)
A constitutively active and nuclear form of the MAP kinase ERK2 is sufficient for neurite outgrowth and cell transformation
M J Robinson et al. Curr Biol. 1998.
Free article
Abstract
Background: Mitogen-activated protein (MAP) kinases are ubiquitous components of many signal transduction pathways. Constitutively active variants have been isolated for every component of the extracellular-signal-regulated kinase 1 (ERK1) and ERK2 MAP kinase pathway except for the ERK itself.
Results: To create an activated ERK2 variant, we fused ERK2 to the low activity form of its upstream regulator, the MAP kinase kinase MEK1. The ERK2 in this fusion protein was active in the absence of extracellular signals. Expression of the fusion protein in mammalian cells did not activate endogenous ERK1 or ERK2. It was sufficient, however, to induce activation of the transcription factors Elk-1 and AP-1, neurite extension in PC12 cells in the absence of nerve growth factor, and foci of morphologically and growth-transformed NIH3T3 cells, if the fusion protein was localized to the nucleus. A cytoplasmic fusion protein was without effect.
Conclusions: Activation of ERK2 is sufficient to cause several transcriptional and phenotypic responses in mammalian cells. Nuclear localization of activated ERK2 is required to induce these events.
Similar articles
- Simian virus 40 small t antigen cooperates with mitogen-activated kinases to stimulate AP-1 activity.
Frost JA, Alberts AS, Sontag E, Guan K, Mumby MC, Feramisco JR. Frost JA, et al. Mol Cell Biol. 1994 Sep;14(9):6244-52. doi: 10.1128/mcb.14.9.6244-6252.1994. Mol Cell Biol. 1994. PMID: 8065356 Free PMC article. - Nuclear export of the stress-activated protein kinase p38 mediated by its substrate MAPKAP kinase-2.
Ben-Levy R, Hooper S, Wilson R, Paterson HF, Marshall CJ. Ben-Levy R, et al. Curr Biol. 1998 Sep 24;8(19):1049-57. doi: 10.1016/s0960-9822(98)70442-7. Curr Biol. 1998. PMID: 9768359 Review. - Structural analysis of the MAP kinase ERK2 and studies of MAP kinase regulatory pathways.
Cobb MH, Xu S, Cheng M, Ebert D, Robbins D, Goldsmith E, Robinson M. Cobb MH, et al. Adv Pharmacol. 1996;36:49-65. doi: 10.1016/s1054-3589(08)60576-1. Adv Pharmacol. 1996. PMID: 8783554 Review. No abstract available.
Cited by
- Cholinergic signaling via muscarinic M1 receptor confers resistance to docetaxel in prostate cancer.
Wang J, Wei J, Pu T, Zeng A, Karthikeyan V, Bechtold B, Vo K, Chen J, Lin TP, Chang AP, Corey E, Puhr M, Klocker H, Culig Z, Bland T, Wu BJ. Wang J, et al. Cell Rep Med. 2024 Feb 20;5(2):101388. doi: 10.1016/j.xcrm.2023.101388. Epub 2024 Jan 22. Cell Rep Med. 2024. PMID: 38262412 Free PMC article. - DCX, a new mediator of the JNK pathway.
Gdalyahu A, Ghosh I, Levy T, Sapir T, Sapoznik S, Fishler Y, Azoulai D, Reiner O. Gdalyahu A, et al. EMBO J. 2004 Feb 25;23(4):823-32. doi: 10.1038/sj.emboj.7600079. Epub 2004 Feb 5. EMBO J. 2004. PMID: 14765123 Free PMC article. - Transforming growth factor-β downregulates sGC subunit expression in pulmonary artery smooth muscle cells via MEK and ERK signaling.
Du L, Roberts JD Jr. Du L, et al. Am J Physiol Lung Cell Mol Physiol. 2019 Jan 1;316(1):L20-L34. doi: 10.1152/ajplung.00319.2018. Epub 2018 Sep 27. Am J Physiol Lung Cell Mol Physiol. 2019. PMID: 30260287 Free PMC article. - ERK and JNK activation is essential for oncogenic transformation by v-Rel.
Kralova J, Sheely JI, Liss AS, Bose HR Jr. Kralova J, et al. Oncogene. 2010 Nov 25;29(47):6267-79. doi: 10.1038/onc.2010.359. Epub 2010 Aug 30. Oncogene. 2010. PMID: 20802521 Free PMC article. - System theoretical investigation of human epidermal growth factor receptor-mediated signalling.
Zhang Y, Shankaran H, Opresko L, Resat H. Zhang Y, et al. IET Syst Biol. 2008 Sep;2(5):273-84. doi: 10.1049/iet-syb:20080116. IET Syst Biol. 2008. PMID: 19045822 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous