Literature DB >> 8377220

Specific regulation of immediate early genes by patterned neuronal activity.

H Z Sheng1, R D Fields, P G Nelson.   

Abstract

Electrical activity shapes development of the nervous system, presumably in part by regulating gene expression. A set of regulatory genes, immediate early genes (IEGs), which are responsive to a number of extrinsic cellular stimuli have been proposed to play a role in coupling such activity to gene expression. Using a semiquantitative polymerase chain reaction assay, we show that in dissociated mouse dorsal root ganglion neurons the expression of two IEGs, c-fos and nur/77, is differentially sensitive to patterns of electrical stimulation. Differences in c-fos activation did not correlate with the peak intracellular calcium [Ca++]i produced by the different stimulation patterns or with residual [Ca++]i following stimulation. However, the net increase in [Ca++]i (calcium time integral) was greater for the pulsed stimulus that activated c-fos (6 impulses/min), compared to the ineffective stimulus (12 impulses/2 min). This system of genes seems suited to mediating the coupling between electrical activity and other functional genes.

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Year:  1993        PMID: 8377220     DOI: 10.1002/jnr.490350502

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  19 in total

1.  Spike frequency decoding and autonomous activation of Ca2+-calmodulin-dependent protein kinase II in dorsal root ganglion neurons.

Authors:  F Eshete; R D Fields
Journal:  J Neurosci       Date:  2001-09-01       Impact factor: 6.167

2.  The use of oscillatory signals in the study of genetic networks.

Authors:  Ovidiu Lipan; Wing H Wong
Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-09       Impact factor: 11.205

3.  CaMKII inactivation by extracellular Ca(2+) depletion in dorsal root ganglion neurons.

Authors:  Jonathan E Cohen; R Douglas Fields
Journal:  Cell Calcium       Date:  2006-03-07       Impact factor: 6.817

4.  Neurons in a forebrain nucleus required for vocal plasticity rapidly switch between precise firing and variable bursting depending on social context.

Authors:  Mimi H Kao; Brian D Wright; Allison J Doupe
Journal:  J Neurosci       Date:  2008-12-03       Impact factor: 6.167

5.  Control of time-dependent biological processes by temporally patterned input.

Authors:  V Brezina; I V Orekhova; K R Weiss
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-16       Impact factor: 11.205

6.  Action potential-dependent regulation of gene expression: temporal specificity in ca2+, cAMP-responsive element binding proteins, and mitogen-activated protein kinase signaling.

Authors:  R D Fields; F Eshete; B Stevens; K Itoh
Journal:  J Neurosci       Date:  1997-10-01       Impact factor: 6.167

7.  Different Neuronal Activity Patterns Induce Different Gene Expression Programs.

Authors:  Kelsey M Tyssowski; Nicholas R DeStefino; Jin-Hyung Cho; Carissa J Dunn; Robert G Poston; Crista E Carty; Richard D Jones; Sarah M Chang; Palmyra Romeo; Mary K Wurzelmann; James M Ward; Mark L Andermann; Ramendra N Saha; Serena M Dudek; Jesse M Gray
Journal:  Neuron       Date:  2018-04-19       Impact factor: 17.173

Review 8.  The neuronal stimulation-transcription coupling map.

Authors:  Kelsey M Tyssowski; Jesse M Gray
Journal:  Curr Opin Neurobiol       Date:  2019-06-01       Impact factor: 6.627

9.  Neuronal Circuit Activity during Neonatal Hypoxic-Ischemic Seizures in Mice.

Authors:  Jennifer Burnsed; Daria Skwarzyńska; Pravin K Wagley; Laura Isbell; Jaideep Kapur
Journal:  Ann Neurol       Date:  2019-10-18       Impact factor: 10.422

10.  Expression of c-fos in hilar mossy cells of the dentate gyrus in vivo.

Authors:  Aine M Duffy; Michael J Schaner; Jeannie Chin; Helen E Scharfman
Journal:  Hippocampus       Date:  2013-05-27       Impact factor: 3.899

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