Response Modulation in the Zebra Finch Neostriatum: Relationship to Nuclear Gene Regulation

The sound of birdsong activates robust gene expression in the caudomedial neostriatum (NCM) of songbirds. To assess the function of this genomic response, we analyzed the temporal and quantitative relationships between electrophysiological activity and gene induction. Single units in zebra finch NCM showed large increases in firing in response to birdsong, whereas simple auditory tones tended to inhibit firing. Most cells showed little selectivity for individual songs based on total number of spikes produced. When a novel song stimulus was repeated, the cells rapidly modulated their firing rates so that the first response to a stimulus was markedly higher than consecutive responses. Even after many repetitions of a particular song, cells continued to fire in response to that stimulus, unlike the complete “habituation” observed previously for genomic activity. The initial modulation of the response to a particular song disappeared, however, once that song was repeated for 200 trials (∼34 min). These results indicate a dissociation between gross physiological activity and “immediate early” gene expression: genomic activity occurs only during a subset of electrophysiological responses. We propose a model in which nuclear responses in NCM are modulated by pathways distinct from the primary auditory inputs to NCM. This would account for the changing selectivity of the genomic response and implies an active role for the cell nucleus as an integrating agent in the physiological operation of neural circuits.

[1]  S Schoch,et al.  Regulation of synapsin I gene expression by the zinc finger transcription factor zif268/egr-1. , 1994, The Journal of biological chemistry.

[2]  D. Vicario,et al.  Song presentation induces gene expression in the songbird forebrain. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[3]  V. Sukhatme,et al.  Egr-1 activation of rat adrenal phenylethanolamine N-methyltransferase gene. , 1994, The Journal of biological chemistry.

[4]  D Margoliash,et al.  Global synchronous response to autogenous song in zebra finch HVc. , 1994, Journal of neurophysiology.

[5]  S. Volman,et al.  Development of neural selectivity for birdsong during vocal learning , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[6]  F. Nottebohm,et al.  Repeated exposure to one song leads to a rapid and persistent decline in an immediate early gene's response to that song in zebra finch telencephalon , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  D. Margoliash,et al.  Temporal and harmonic combination-sensitive neurons in the zebra finch's HVc , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  Clive K. Catchpole,et al.  9 – The Evolution of Bird Sounds in Relation to Mating and Spacing Behavior , 1982 .

[9]  C. Mello,et al.  Song-induced ZENK gene expression in auditory pathways of songbird brain and its relation to the song control system , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  D. Margoliash Acoustic parameters underlying the responses of song-specific neurons in the white-crowned sparrow , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  Cedric L. Williams,et al.  Neuromodulatory systems and memory storage: Role of the amygdala , 1993, Behavioural Brain Research.

[12]  S J Chew,et al.  A large-capacity memory system that recognizes the calls and songs of individual birds. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[13]  G. E. Vates,et al.  Auditory pathways of caudal telencephalon and their relation to the song system of adult male zebra finches (Taenopygia guttata) , 1996, The Journal of comparative neurology.

[14]  E. Ziff,et al.  Fos family members successively occupy the tyrosine hydroxylase gene AP-1 site after nerve growth factor or epidermal growth factor stimulation and can repress transcription. , 1994, Molecular endocrinology.

[15]  S Schoch,et al.  The Human Synapsin II Gene Promoter , 1995, The Journal of Biological Chemistry.

[16]  H. Leppelsack,et al.  Cell types of the auditory caudomedial neostriatum of the starling (Sturnus vulgaris) , 1981, The Journal of comparative neurology.

[17]  A. Seasholtz,et al.  The cAMP-responsive element in the corticotropin-releasing hormone gene mediates transcriptional regulation by depolarization. , 1994, The Journal of biological chemistry.

[18]  L. Squire,et al.  Protein synthesis and memory: a review. , 1984, Psychological bulletin.

[19]  Donald E. Kroodsma,et al.  The Function(s) of Bird Song , 1991 .

[20]  A. Routtenberg,et al.  Induction of F1/GAP-43 gene expression in hippocampal granule cells after seizures [corrected]. , 1993, Brain research. Molecular brain research.

[21]  Joseph E. LeDoux,et al.  Emotional memory systems in the brain , 1993, Behavioural Brain Research.

[22]  C. Vianna,et al.  Analysis of Immediate-Early Gene Expression in the Songbird Brain Following Song Presentation , 1993 .

[23]  C. Mello,et al.  Immediate-early gene responses in the avian song control system: cloning and expression analysis of the canary c-jun cDNA. , 1994, Brain research. Molecular brain research.

[24]  Michael Davis,et al.  Involvement of subcortical and cortical afferents to the lateral nucleus of the amygdala in fear conditioning measured with fear- potentiated startle in rats trained concurrently with auditory and visual conditioned stimuli , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  S. Hyman,et al.  Opioids modulate stress-induced proenkephalin gene expression in the hypothalamus of transgenic mice: A model of endogenous opioid gene regulation by exogenous opioids , 1994, Regulatory Peptides.

[26]  A. Graybiel,et al.  Dynamic regulation of NGFI-A (zif268, egr1) gene expression in the striatum , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[27]  P. Stoddard,et al.  Repertoire matching between neighbouring song sparrows , 1996, Animal Behaviour.

[28]  J. Julien,et al.  AP-1 and Krox-24 transcription factors activate the neurofilament light gene promoter in P19 embryonal carcinoma cells. , 1994, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[29]  D. Margoliash,et al.  Parallel pathways and convergence onto HVc and adjacent neostriatum of adult zebra finches (Taeniopygia guttata) , 1995, The Journal of comparative neurology.

[30]  F. Nottebohm,et al.  Central control of song in the canary, Serinus canarius , 1976, The Journal of comparative neurology.

[31]  M. Baudry,et al.  Synaptotagmin IV is an immediate early gene induced by depolarization in PC12 cells and in brain. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Philip Goelet,et al.  The long and the short of long–term memory—a molecular framework , 1986, Nature.

[33]  Masakazu Konishi,et al.  Birdsong for neurobiologists , 1989, Neuron.