Differential expression of the immediate early genes FOS and ZENK following auditory stimulation in the juvenile male and female zebra finch

Molecular Brain Research

Volumn 116, Issue 1-2, 2003, Pages 147-154

  Bailey, David J ^a   Wade, Juli ^a  

^a MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

cHV; Development; Hippocampus; NCM; Perception; Sex difference; Songbird

Indexed keywords

ARTICLE; AUDITORY STIMULATION; CONTROLLED STUDY; CORPUS STRIATUM; FEMALE; GENE EXPRESSION; HIPPOCAMPUS; IMMUNOREACTIVITY; JUVENILE; MALE; NERVE CELL; NONHUMAN; PERCEPTION; PRIORITY JOURNAL; STIMULUS RESPONSE; ZEBRA FISH;

FRINGILLIDAE; PASSERI; TAENIOPYGIA; TAENIOPYGIA GUTTATA;

EID: 0042020009     PISSN: 0169328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0169-328X(03)00288-2     Document Type: Article

References (28)

1. Arnold A.P. Sexual differentiation of the zebra finch song system: Positive evidence, negative evidence, null hypotheses, and a paradigm shift. J. Neurobiol. 33:1997;572-584.
2. Bailey D.J., Rosebush J.C., Wade J. The hippocampus and caudomedial neostriatum show selective responsiveness to conspecific song in the female zebra finch. J. Neurobiol. 52:2002;43-51.
3. Bolhuis J.J., Hetebrij E., den Boer-Visser A.M., De Groot J.H., Zijlstra G.G.O. Localized immediate early gene expression related to the strength of song learning in socially reared zebra finches. Eur. J. Neurosci. 13:2001;2165-2170.
4. Bolhuis J.J., Zijlstra G.G.O., den Boer-Visser A.M., Van der Zee E.A. Localized neuronal activation in the zebra finch brain is related to the strength of song learning. Proc. Natl. Acad. Sci. USA. 97:2000;2282-2285.
5. Clayton N.S. Song discrimination learning in zebra finches. Anim. Behav. 36:1988;1016-1024.
6. D'Hondt E., Vermeiren J., Peeters K., Balthazart J., Tlemcani O., Ball G.F., Duffy D.L., Vandesande F., Berghman L.R. Validation of a new antiserum directed towards the synthetic c-terminus of the FOS protein in avian species: immunological, physiological and behavioral evidence. J Neurosci. Methods. 91:1999;31-45.
7. Duffy D.L., Bentley G.E., Ball G.F. Does sex or photoperiodic condition influence ZENK induction in response to song in European starlings? Brain Res. 844:1999;78-82.
8. Jarvis E.D., Nottebohm F. Motor-driven gene expression. Proc. Natl. Acad. Sci. USA. 94:1997;4097-4102.
9. Jin H., Clayton D.F. Localized changes in immediate-early gene regulation during sensory and motor learning in zebra finches. Neuron. 19:1997;1049-1059.
10. Kimpo R.R., Doupe A.J. Fos is induced by singing in distinct neuronal populations in a motor network. Neuron. 18:1997;315-325.
11. Kroodsma D.E. Suggested experimental designs for song playbacks. Anim. Behav. 37:1989;600-609.
12. Kroodsma D.E., Byers B.E., Goodale E., Johnson S., Liu W.-C. Pseudoreplication in playback experiments, revisited a decade later. Anim. Behav. 61:2001;1029-1033.
13. Kruse A.A., Stripling R., Clayton D.F. Minimal experience required for immediate-early gene induction in zebra finch neostriatum. Neurobiol. Learn. Mem. 74:2000;179-184.
14. Lewicki M.S., Konishi M. Mechanisms underlying the sensitivity of songbird forebrain neurons to temporal order. Proc. Natl. Acad. Sci. USA. 92:1995;5582-5586.
15. Margoliash D., Fortune E.S. Temporal and harmonic combination-sensitive neurons in the zebra finch's HVc. J. Neurosci. 12:1992;4309-4326.
16. Mello C.V., Vicario D.S., Clayton D.F. Song presentation induces gene expression in the songbird forebrain. Proc. Natl. Acad. Sci. USA. 89:1992;6818-6822.
17. Mello C.V., Clayton D.F. Song-induced ZENK gene expression in auditory pathways of songbird brain and its relation to the song control system. J. Neurosci. 14:1994;6652-6666.
18. Mello C.V., Nottebohm F., Clayton D.F. 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. J. Neurosci. 15:1995;6919-6925.
19. Mello C.V., Ribeiro S. ZENK protein regulation by song in the brain of songbirds. J. Comp. Neurol. 393:1998;426-438.
20. Miller D.B. Long-term recognition of father's song by female zebra finches. Nature. 280:1979;389-391.
21. Nealen P.M., Schmidt M.F. Comparative approaches to avian song system function: insights into auditory and motor processing. J. Comp. Physiol. A. 188:2002;929-941.
22. Nordeen K.W., Nordeen E.J. Anatomical and synaptic substrates for avian song learning. J. Neurobiol. 33:1997;532-548.
23. Nottebohm F., Arnold A.P. Sexual dimorphism in vocal control areas of the songbird brain. Science. 194:1976;211-213.
24. Stripling R., Kruse A.A., Clayton D.F. Development of song responses in the zebra finch caudomedial neostriatum: role of genomic and electrophysiological activities. J. Neurobiol. 48:2001;163-180.
25. Szekely A.D., Krebs J.R. Efferent connectivity of the hippocampal formation of the zebra finch (Taenopygia guttata): an anterograde pathway tracing study using Phaseolus vulgaris leucoagglutinin. J. Comp. Neurol. 368:1996;198-214.
26. Szekely A.D. The avian hippocampal formation: subdivisions and connectivity. Behav. Brain Res. 98:1999;219-225.
27. Wade J. Zebra finch sexual differentiation: the aromatization hypothesis revisited. Microsc. Res. Tech. 54:2001;354-363.
28. Wade J., Buhlman L. Lateralization and effects of adult androgen in a sexually dimorphic neuromuscular system controlling song in zebra finches. J. Comp. Neurol. 426:2000;154-164.