Brauth Steven, Liang Wenru, Roberts Todd F, Scott Lindsey L, Quinlan Elizabeth M
Department of Psychology, University of Maryland, College Park, Maryland 20742, USA.
Learn Mem. 2002 Mar-Apr;9(2):76-88. doi: 10.1101/lm.40802.
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.
在一种会发声学习的鹦鹉——虎皮鹦鹉(Melopsittacus undulatus)中,当实验对象收听陌生接触叫声的回放或之前已熟悉的接触叫声时,即刻早期基因蛋白Zenk(zif 268、egr - 1、NGF1A、Krox24)在前脑听觉核中被诱导表达。听觉核包括L区复合体(L1、L2a和L3)、新纹状体中间部腹外侧区(NIVL)、与基底核尾部相邻的新纹状体(基底周或pBas)、额叶外侧新纹状体中的一个区域(NFl)、外侧新纹状体的中央上核(NLs)以及腹内侧纹状体腹侧部(HVvm)。后三个核是听觉系统向发声系统输入信息的主要来源。接触叫声刺激诱导出两种核染色模式——整个细胞核染色,除L2a外,所有检测区域中至少一些神经元呈现这种染色;核仁周围染色,这是L2a区域唯一呈现的染色类型。Zenk染色的不同模式表明,听觉刺激可能在不同听觉核中调节与Zenk相关的不同基因子集的转录。当鸟类收听重复的陌生叫声时,表达Zenk染色的神经元数量比对照水平增加了7至43倍。通过重复回放使实验对象熟悉叫声刺激后,当在间隔24小时后再次呈现该叫声时,Zenk表达的诱导显著减少。为了确定表现出接触叫声驱动的Zenk表达的神经元是否投射到发声控制系统,将叫声刺激与葡聚糖胺通路追踪相结合。结果表明,在发声核HVo(纹状体腹侧卵圆核)、HVo外侧区域和NLs中注射示踪剂,标记了HVvm、NFl和NLs中许多Zenk阳性神经元。这些结果支持了这样一种观点,即在这些神经元中,egr - 1将听觉刺激与参与为发声学习存储新感知记忆痕迹、处理与发声学习或其发生背景相关的新颖和/或有意义的声学刺激的蛋白质合成联系起来。