Literature DB >> 11992018

Contact call-driven Zenk protein induction and habituation in telencephalic auditory pathways in the Budgerigar (Melopsittacus undulatus): implications for understanding vocal learning processes.

Steven Brauth1, Wenru Liang, Todd F Roberts, Lindsey L Scott, Elizabeth M Quinlan.   

Abstract

Expression of the immediate early gene protein Zenk (zif 268, egr-1, NGF1A, Krox24) was induced in forebrain auditory nuclei in a vocal learning parrot species, the budgerigar (Melopsittacus undulatus), when the subjects either listened to playbacks of an unfamiliar contact call or to a contact call with which they had been familiarized previously. Auditory nuclei included the Field L complex (L1, L2a, and L3), the neostriatum intermedium pars ventrolateralis (NIVL), the neostriatum adjacent to caudal nucleus basalis (peri-basalis or pBas), an area in the frontal lateral neostriatum (NFl), the supracentral nucleus of the lateral neostriatum (NLs), and the ventromedial hyperstriatum ventrale (HVvm). The latter three nuclei are main sources of auditory input to the vocal system. Two patterns of nuclear staining were induced by contact call stimulation-staining throughout cell nuclei, which was exhibited by at least some neurons in all areas examined except L2a and perinucleolar staining, which was the only kind of staining exhibited in field L2a. The different patterns of Zenk staining indicate that auditory stimulation may regulate the Zenk-dependent transcription of different subsets of genes in different auditory nuclei. The numbers of neurons expressing Zenk staining increased from seven- to 43-fold over control levels when the birds listened to a repeating unfamiliar call. Familiarization of the subjects with the call stimulus, through repeated playbacks, greatly reduced the induction of Zenk expression to the call when it was presented again after an intervening 24-h interval. To determine if neurons exhibiting contact call-driven Zenk expression project to the vocal control system, call stimulation was coupled with dextran amines pathway tracing. The results indicated that tracer injections in the vocal nucleus HVo (oval nucleus of the hyperstriatum ventrale), in fields lateral to HVo and in NLs labeled many Zenk-positive neurons in HVvm, NFl, and NLs. These results support the idea that, in these neurons, egr-1 couples auditory stimulation to the synthesis of proteins involved in either the storing of new perceptual engrams for vocal learning or the processing of novel and/or meaningful acoustic stimuli related to vocal learning or the context in which it occurs.

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Year:  2002        PMID: 11992018      PMCID: PMC155933          DOI: 10.1101/lm.40802

Source DB:  PubMed          Journal:  Learn Mem        ISSN: 1072-0502            Impact factor:   2.460


  53 in total

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Journal:  Neurobiol Learn Mem       Date:  2000-11       Impact factor: 2.877

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Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

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Journal:  J Neurobiol       Date:  1995-01

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Journal:  Brain Res       Date:  1968-10       Impact factor: 3.252

8.  Molecular mapping of brain areas involved in parrot vocal communication.

Authors:  E D Jarvis; C V Mello
Journal:  J Comp Neurol       Date:  2000-03-27       Impact factor: 3.215

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Authors:  W S Hall; P L Cohen; S E Brauth
Journal:  Brain Behav Evol       Date:  1993       Impact factor: 1.808

10.  Auditory pathways in the budgerigar. II. Intratelencephalic pathways.

Authors:  S E Brauth; C M McHale
Journal:  Brain Behav Evol       Date:  1988       Impact factor: 1.808

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  6 in total

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Journal:  Learn Mem       Date:  2005 Mar-Apr       Impact factor: 2.460

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Authors:  Kendra B Sewall; Anna M Young; Timothy F Wright
Journal:  Anim Behav       Date:  2016-09-07       Impact factor: 2.844

3.  Localized brain activation related to the strength of auditory learning in a parrot.

Authors:  Hiroko Eda-Fujiwara; Takuya Imagawa; Masanori Matsushita; Yasushi Matsuda; Hiro-Aki Takeuchi; Ryohei Satoh; Aiko Watanabe; Matthijs A Zandbergen; Kazuchika Manabe; Takashi Kawashima; Johan J Bolhuis
Journal:  PLoS One       Date:  2012-06-11       Impact factor: 3.240

4.  Differences in number and distribution of striatal calbindin medium spiny neurons between a vocal-learner (Melopsittacus undulatus) and a non-vocal learner bird (Colinus virginianus).

Authors:  Elena Garcia-Calero; Olga Bahamonde; Salvador Martinez
Journal:  Front Neuroanat       Date:  2013-12-19       Impact factor: 3.856

5.  Sex differences in behavioural and neural responsiveness to mate calls in a parrot.

Authors:  Hiroko Eda-Fujiwara; Ryohei Satoh; Yuka Hata; Marika Yamasaki; Aiko Watanabe; Matthijs A Zandbergen; Yasuharu Okamoto; Takenori Miyamoto; Johan J Bolhuis
Journal:  Sci Rep       Date:  2016-01-04       Impact factor: 4.379

6.  Memory-specific correlated neuronal activity in higher-order auditory regions of a parrot.

Authors:  Ryohei Satoh; Hiroko Eda-Fujiwara; Aiko Watanabe; Yasuharu Okamoto; Takenori Miyamoto; Matthijs A Zandbergen; Johan J Bolhuis
Journal:  Sci Rep       Date:  2021-01-15       Impact factor: 4.379

  6 in total

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