Allele-specific cis-regulatory methylation of the gene for vasoactive intestinal peptide in white-throated sparrows

IF 2.4 4区 心理学 Q2 BEHAVIORAL SCIENCES
Mackenzie R. Prichard, Kathleen E. Grogan, Jennifer R. Merritt, Jessica Root, Donna L. Maney
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引用次数: 2

Abstract

White-throated sparrows (Zonotrichia albicollis) offer a unique opportunity to connect genotype with behavioral phenotype. In this species, a rearrangement of the second chromosome is linked with territorial aggression; birds with a copy of this “supergene” rearrangement are more aggressive than those without it. The supergene has captured the gene VIP, which encodes vasoactive intestinal peptide, a neuromodulator that drives aggression in other songbirds. In white-throated sparrows, VIP expression is higher in the anterior hypothalamus of birds with the supergene than those without it, and expression of VIP in this region predicts the level of territorial aggression regardless of genotype. Here, we aimed to identify epigenetic mechanisms that could contribute to differential expression of VIP both in breeding adults, which exhibit morph differences in territorial aggression, and in nestlings, before territorial behavior develops. We extracted and bisulfite-converted DNA from samples of the hypothalamus in wild-caught adults and nestlings and used high-throughput sequencing to measure DNA methylation of a region upstream of the VIP start site. We found that the allele inside the supergene was less methylated than the alternative allele in both adults and nestlings. The differential methylation was attributed primarily to CpG sites that were shared between the alleles, not to polymorphic sites, which suggests that epigenetic regulation is occurring independently of the genetic differentiation within the supergene. This work represents an initial step toward understanding how epigenetic differentiation inside chromosomal inversions leads to the development of alternative behavioral phenotypes.

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白喉麻雀血管活性肠肽基因等位基因特异性顺式调控甲基化
白喉麻雀提供了一个独特的机会,将基因型与行为表型联系起来。在这个物种中,第二条染色体的重排与领土侵略有关;拥有这种“超级基因”重排的鸟类比没有这种基因的鸟类更具攻击性。超级基因捕获了VIP基因,该基因编码血管活性肠肽,这是一种神经调节剂,可以驱动其他鸣禽的攻击性。在白喉麻雀中,携带该超基因的鸟类下丘脑前部VIP的表达高于不携带该超基因的鸟类,该区域VIP的表达预示着不同基因型的领土侵略水平。在这里,我们的目的是确定表观遗传机制,可能导致VIP在繁殖成虫和雏鸟中表达的差异,它们在领土攻击方面表现出形态差异,在领土行为发展之前。我们从野生捕获的成年和雏鸟的下丘脑样本中提取和亚硫酸盐转化的DNA,并使用高通量测序来测量VIP起始位点上游区域的DNA甲基化。我们发现,在成年和雏鸟中,超基因内的等位基因甲基化程度低于替代等位基因。差异甲基化主要归因于等位基因之间共享的CpG位点,而不是多态性位点,这表明表观遗传调控独立于超基因内的遗传分化发生。这项工作代表了理解染色体倒位内的表观遗传分化如何导致替代行为表型的发展的第一步。
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来源期刊
Genes Brain and Behavior
Genes Brain and Behavior 医学-行为科学
CiteScore
6.80
自引率
4.00%
发文量
62
审稿时长
4-8 weeks
期刊介绍: Genes, Brain and Behavior was launched in 2002 with the aim of publishing top quality research in behavioral and neural genetics in their broadest sense. The emphasis is on the analysis of the behavioral and neural phenotypes under consideration, the unifying theme being the genetic approach as a tool to increase our understanding of these phenotypes. Genes Brain and Behavior is pleased to offer the following features: 8 issues per year online submissions with first editorial decisions within 3-4 weeks and fast publication at Wiley-Blackwells High visibility through its coverage by PubMed/Medline, Current Contents and other major abstracting and indexing services Inclusion in the Wiley-Blackwell consortial license, extending readership to thousands of international libraries and institutions A large and varied editorial board comprising of international specialists.
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