CHIRP-Seq: FOXP2 transcriptional targets in zebra finch brain include numerous speech and language-related genes.

IF 2.4 4区 医学 Q3 NEUROSCIENCES
Gregory L Gedman, Todd H Kimball, Lee L Atkinson, Daniella Factor, Gabriela Vojtova, Madza Farias-Virgens, Timothy F Wright, Stephanie A White
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引用次数: 0

Abstract

Background: Vocal learning is a rare, convergent trait that is fundamental to both human speech and birdsong. The Forkhead Box P2 (FOXP2) transcription factor appears necessary for both types of learned signals, as human mutations in FOXP2 result in speech deficits, and disrupting its expression in zebra finches impairs male-specific song learning. In juvenile and adult male finches, striatal FOXP2 mRNA and protein decline acutely within song-dedicated neurons during singing, indicating that its transcriptional targets are also behaviorally regulated. The identities of these targets in songbirds, and whether they differ across sex, development and/or behavioral conditions, are largely unknown.

Results: Here we used chromatin immunoprecipitation followed by sequencing (ChIP-Seq) to identify genomic sites bound by FOXP2 in male and female, juvenile and adult, and singing and non-singing birds. Our results suggest robust FOXP2 binding concentrated in putative promoter regions of genes. The number of genes likely to be bound by FOXP2 varied across conditions, suggesting specialized roles of the candidate targets related to sex, age, and behavioral state. We interrogated these binding targets both bioinformatically, with comparisons to previous studies, and biochemically, with immunohistochemistry using an antibody for a putative target gene. Gene ontology analyses revealed enrichment for human speech- and language-related functions in males only, consistent with the sexual dimorphism of song learning in this species. Fewer such targets were found in juveniles relative to adults, suggesting an expansion of this regulatory network with maturation. The fewest speech-related targets were found in the singing condition, consistent with the well-documented singing-driven down-regulation of FOXP2 in the songbird striatum.

Conclusions: Overall, these data provide an initial catalog of the regulatory landscape of FOXP2 in an avian vocal learner, offering dozens of target genes for future study and providing insight into the molecular underpinnings of vocal learning.

CHIRP-Seq:斑胸草雀大脑中的FOXP2转录靶点包括许多语音和语言相关基因。
背景:声乐学习是一种罕见的、趋同的特征,是人类语言和鸟类歌唱的基础。叉头盒P2 (FOXP2)转录因子似乎对这两种类型的学习信号都是必需的,因为人类FOXP2的突变会导致语言缺陷,而在斑胸草雀中破坏其表达会损害雄性特有的鸣叫学习。在幼鸟和成年雄性雀中,歌唱专用神经元的纹状体FOXP2 mRNA和蛋白在鸣叫过程中急剧下降,表明其转录靶点也受到行为调控。鸣禽中这些靶标的身份,以及它们在性别、发育和/或行为条件上是否存在差异,在很大程度上是未知的。结果:本研究采用染色质免疫沉淀-测序(ChIP-Seq)技术鉴定了雄性和雌性、幼鸟和成鸟、鸣禽和非鸣禽中FOXP2结合的基因组位点。我们的结果表明FOXP2结合集中在假定的基因启动子区域。FOXP2可能结合的基因数量在不同的条件下有所不同,这表明候选靶点的特殊作用与性别、年龄和行为状态有关。我们对这些结合靶点进行了生物信息学研究,与之前的研究进行了比较,并使用生物化学方法,使用免疫组织化学方法对假定的靶基因进行了抗体检测。基因本体论分析显示,人类语言和语言相关功能仅在雄性中丰富,这与该物种鸣叫学习的两性二态性一致。与成年鱼相比,在幼鱼身上发现的这类靶标较少,这表明这种调节网络随着成熟而扩大。在歌唱条件下发现的与语言相关的靶标最少,这与有充分记录的歌唱驱动的鸣禽纹状体中FOXP2的下调一致。结论:总的来说,这些数据提供了FOXP2在鸟类声乐学习者中的调控格局的初步目录,为未来的研究提供了数十个靶基因,并为声乐学习的分子基础提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Neuroscience
BMC Neuroscience 医学-神经科学
CiteScore
3.90
自引率
0.00%
发文量
64
审稿时长
16 months
期刊介绍: BMC Neuroscience is an open access, peer-reviewed journal that considers articles on all aspects of neuroscience, welcoming studies that provide insight into the molecular, cellular, developmental, genetic and genomic, systems, network, cognitive and behavioral aspects of nervous system function in both health and disease. Both experimental and theoretical studies are within scope, as are studies that describe methodological approaches to monitoring or manipulating nervous system function.
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