In Vivo Expression and Regulation of Elk-1, a Target of the Extracellular-Regulated Kinase Signaling Pathway, in the Adult Rat Brain

The transcription factor Elk-1, a nuclear target of extracellular-regulated kinases (ERKs), plays a pivotal role in immediate early gene induction by external stimuli. Notably, the degree of phosphorylation of Elk-1 is tightly correlated with the level of activation of transcription of c-fos by proliferative signals. No data yet indicate the role of Elk-1 in the adult brainin vivo. To address this question, we have analyzed in the present work (1) Elk-1 mRNA and protein expression in the adult rat brain, and (2) the regulation of Elk-1 (i.e., its phosphorylation state) in an in vivo model of immediate early gene (IEG) induction: an electrical stimulation of the cerebral cortex leading to c-fos and zif268 mRNA induction in the striatum. Using in situ hybridization, we show that Elk-1 mRNA is expressed in various brain structures of adult rat, and that this expression is exclusively neuronal. We demonstrate by immunocytochemistry using various specific Elk-1 antisera that the protein is not only nuclear (as shown previously in transiently transfected cell lines) but is also present in soma, dendrites, and axon terminals. On electrical stimulation of the glutamatergic corticostriatal pathway, we show a strict spatiotemporal correspondence among ERK activation, Elk-1 phosphorylation, and IEG mRNA induction. Furthermore, both activated proteins, analyzed by immunocytochemistry, are found in cytosolic and nuclear comparments of neuronal cells in the activated area. Our data suggest that the ERK signaling pathway plays an important role in regulating genes controlled by serum response element sites via phosphorylation of Elk-1 in vivo.

[1]  J. Deniau,et al.  Effect of electrical stimulation of the cerebral cortex on the expression of the fos protein in the basal ganglia , 1997, Neuroscience.

[2]  Eric R Kandel,et al.  MAP Kinase Translocates into the Nucleus of the Presynaptic Cell and Is Required for Long-Term Facilitation in Aplysia , 1997, Neuron.

[3]  D. Ginty,et al.  Calcium Regulation of Gene Expression: Isn't That Spatial? , 1997, Neuron.

[4]  Hilmar Bading,et al.  Distinct functions of nuclear and cytoplasmic calcium in the control of gene expression , 1997, Nature.

[5]  J. Girault,et al.  Differential Regulation of Proline-rich Tyrosine Kinase 2/Cell Adhesion Kinase β (PYK2/CAKβ) and pp125FAK by Glutamate and Depolarization in Rat Hippocampus* , 1996, The Journal of Biological Chemistry.

[6]  J. David Sweatt,et al.  Activation of p42 Mitogen-activated Protein Kinase in Hippocampal Long Term Potentiation* , 1996, The Journal of Biological Chemistry.

[7]  M. Greenberg,et al.  Calcium Influx via the NMDA Receptor Induces Immediate Early Gene Transcription by a MAP Kinase/ERK-Dependent Mechanism , 1996, The Journal of Neuroscience.

[8]  Michael E. Greenberg,et al.  Coupling of the RAS-MAPK Pathway to Gene Activation by RSK2, a Growth Factor-Regulated CREB Kinase , 1996, Science.

[9]  R. Davis,et al.  MKK3- and MKK6-regulated gene expression is mediated by the p38 mitogen-activated protein kinase signal transduction pathway , 1996, Molecular and cellular biology.

[10]  F. Ferraguti,et al.  Stress activated protein kinases, a novel family of mitogen-activated protein kinases, are heterogeneously expressed in the adult rat brain and differentially distributed from extracellular-signal-regulated protein kinases , 1995, Neuroscience.

[11]  M. Karin,et al.  Induction of c‐fos expression through JNK‐mediated TCF/Elk‐1 phosphorylation. , 1995, The EMBO journal.

[12]  Michael E. Greenberg,et al.  Opposing Effects of ERK and JNK-p38 MAP Kinases on Apoptosis , 1995, Science.

[13]  R. Treisman Journey to the surface of the cell: Fos regulation and the SRE. , 1995, The EMBO journal.

[14]  R. Hipskind,et al.  Protein synthesis inhibitors reveal differential regulation of mitogen-activated protein kinase and stress-activated protein kinase pathways that converge on Elk-1 , 1995, Molecular and cellular biology.

[15]  K. Fukunaga,et al.  Activation of Mitogen‐Activated Protein Kinase in Cultured Rat Hippocampal Neurons by Stimulation of Glutamate Receptors , 1995, Journal of neurochemistry.

[16]  E. Peles,et al.  Protein tyrosine kinase PYK2 involved in Ca2+-induced regulation of ion channel and MAP kinase functions , 1995, Nature.

[17]  M. Crouch,et al.  Retrograde axonal transport of signal transduction proteins in rat sciatic nerve , 1995, Brain Research.

[18]  M. Greenberg,et al.  Calcium activates serum response factor-dependent transcription by a Ras- and Elk-1-independent mechanism that involves a Ca2+/calmodulin-dependent kinase , 1995, Molecular and cellular biology.

[19]  R. Treisman,et al.  Comparative analysis of the ternary complex factors Elk‐1, SAP‐1a and SAP‐2 (ERP/NET). , 1995, The EMBO journal.

[20]  E. Krebs,et al.  The MAPK signaling cascade , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[21]  M E Greenberg,et al.  Calcium signaling in neurons: molecular mechanisms and cellular consequences. , 1995, Science.

[22]  C. Slaughter,et al.  ERK phosphorylation potentiates Elk‐1‐mediated ternary complex formation and transactivation. , 1995, The EMBO journal.

[23]  Richard J Smeyne,et al.  Regulation of c-fos expression in transgenic mice requires multiple interdependent transcription control elements , 1995, Neuron.

[24]  H. W. Harris,et al.  Extracellular signal-regulated protein kinases (ERKs) and ERK kinase (MEK) in brain: regional distribution and regulation by chronic morphine , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  L. Mahadevan,et al.  Anisomycin-activated protein kinases p45 and p55 but not mitogen-activated protein kinases ERK-1 and -2 are implicated in the induction of c-fos and c-jun , 1994, Molecular and cellular biology.

[26]  J. Woodgett,et al.  The stress-activated protein kinases are major c-Jun amino-terminal kinases activated by ischemia and reperfusion. , 1994, The Journal of biological chemistry.

[27]  R. Hipskind,et al.  Heterogeneity of ternary complex factors in HeLa cell nuclear extracts. , 1994, The Journal of biological chemistry.

[28]  R. Hipskind,et al.  Transient activation of RAF-1, MEK, and ERK2 coincides kinetically with ternary complex factor phosphorylation and immediate-early gene promoter activity in vivo , 1994, Molecular and cellular biology.

[29]  R. Hipskind,et al.  Ras/MAP kinase-dependent and -independent signaling pathways target distinct ternary complex factors. , 1994, Genes & development.

[30]  B. Wasylyk,et al.  Net, a new ets transcription factor that is activated by Ras. , 1994, Genes & development.

[31]  J. Darnell,et al.  Jak-STAT pathways and transcriptional activation in response to IFNs and other extracellular signaling proteins. , 1994, Science.

[32]  T. Libermann,et al.  ERP, a new member of the ets transcription factor/oncoprotein family: cloning, characterization, and differential expression during B-lymphocyte development , 1994, Molecular and cellular biology.

[33]  A. Nordheim,et al.  Functional dissection of the transcription factor Elk-1. , 1994, Oncogene.

[34]  M. Karin,et al.  JNK1: A protein kinase stimulated by UV light and Ha-Ras that binds and phosphorylates the c-Jun activation domain , 1994, Cell.

[35]  T. Murphy,et al.  Activation of p42 Mitogen‐Activated Protein Kinase by Glutamate Receptor Stimulation in Rat Primary Cortical Cultures , 1993, Journal of neurochemistry.

[36]  S. Hunt,et al.  The regional distribution of extracellularly regulated kinase-1 and -2 messenger RNA in the adult rat central nervous system , 1993, Neuroscience.

[37]  J. Sandkühler,et al.  JUN, FOS, KROX, and CREB transcription factor proteins in the rat cortex: Basal expression and induction by spreading depression and epileptic seizures , 1993, The Journal of comparative neurology.

[38]  Jonathan A. Cooper,et al.  p42 mitogen-activated protein kinase in brain: Prominent localization in neuronal cell bodies and dendrites , 1993, Neuroscience.

[39]  C. Sato-Bigbee,et al.  Presence of a Cyclic AMP Response Element‐Binding Protein in Oligodendrocytes , 1993, Journal of neurochemistry.

[40]  R. Hipskind,et al.  c‐fos transcriptional activation and repression correlate temporally with the phosphorylation status of TCF. , 1993, The EMBO journal.

[41]  R. Treisman,et al.  The SRF accessory protein Elk-1 contains a growth factor-regulated transcriptional activation domain , 1993, Cell.

[42]  Richard Treisman,et al.  Functional analysis of a growth factor-responsive transcription factor complex , 1993, Cell.

[43]  M E Greenberg,et al.  Regulation of gene expression in hippocampal neurons by distinct calcium signaling pathways. , 1993, Science.

[44]  R. Treisman The serum response element. , 1992, Trends in biochemical sciences.

[45]  A. Sharrocks,et al.  Phosphorylation of transcription factor p62TCF by MAP kinase stimulates ternary complex formation at c-fos promoter , 1992, Nature.

[46]  M. Greenberg,et al.  Trans-synaptic regulation of gene expression , 1992, Current Opinion in Neurobiology.

[47]  J. Blenis,et al.  Nuclear localization and regulation of erk- and rsk-encoded protein kinases , 1992, Molecular and cellular biology.

[48]  R. Treisman,et al.  Characterization of SAP-1, a protein recruited by serum response factor to the c-fos serum response element , 1992, Cell.

[49]  V. N. Roa,et al.  Ets-related protein Elk-1 is homologous to the c-fos regulatory factor p62TCF , 1991, Nature.

[50]  M E Greenberg,et al.  Stimulation of protein tyrosine phosphorylation by NMDA receptor activation , 1991, Science.

[51]  A. D. Smith,et al.  The neural network of the basal ganglia as revealed by the study of synaptic connections of identified neurones , 1990, Trends in Neurosciences.

[52]  D. Tank,et al.  Postsynaptic NMDA receptor-mediated calcium accumulation in hippocampal CAl pyramidal cell dendrites , 1990, Nature.

[53]  A. Nordheim,et al.  Synergism in ternary complex formation between the dimeric glycoprotein p67SRF, polypeptide p62TCF and the c‐fos serum response element. , 1990, The EMBO journal.

[54]  M. Greenberg,et al.  The regulation and function of c-fos and other immediate early genes in the nervous system , 1990, Neuron.

[55]  M. Isobe,et al.  elk, tissue-specific ets-related genes on chromosomes X and 14 near translocation breakpoints. , 1989, Science.

[56]  A. Nordheim,et al.  The ability of a ternary complex to form over the serum response element correlates with serum inducibility of the human c-fos promoter , 1989, Cell.

[57]  Richard Treisman,et al.  Isolation and properties of cDNA clones encoding SRF, a transcription factor that binds to the c-fos serum response element , 1988, Cell.

[58]  M. Montminy,et al.  Phosphorylation-induced binding and transcriptional efficacy of nuclear factor CREB , 1988, Nature.

[59]  Richard Treisman,et al.  Identification of a protein-binding site that mediates transcriptional response of the c-fos gene to serum factors , 1986, Cell.

[60]  J. Sweatt,et al.  Activation of p 42 Mitogen-activated Protein Kinase in Hippocampal Long Term Potentiation * , 1996 .

[61]  J. Girault,et al.  Differential regulation of proline-rich tyrosine kinase 2/cell adhesion kinase beta (PYK2/CAKbeta) and pp125(FAK) by glutamate and depolarization in rat hippocampus. , 1996, The Journal of biological chemistry.

[62]  B. Wasylyk,et al.  The Ets family of transcription factors. , 1993, European journal of biochemistry.

[63]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .