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SRX1543306: GSM2045649: Sample_23608_Hyp; Zonotrichia albicollis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 1000) run: 15.3M spots, 3.1G bases, 1.8Gb downloads

Submitted by: NCBI (GEO)
Study: Genes located in a chromosomal inversion are correlated with territorial song in white-throated sparrows
show Abstracthide Abstract
The genome of the white-throated sparrow (Zonotrichia albicollis) contains an inversion polymorphism on chromosome 2 that is linked to predictable variation in a suite of phenotypic traits including plumage color, aggression, and parental behavior. Differences in gene expression between the two color morphs, which represent the two common inversion genotypes (ZAL2/ZAL2 and ZAL2/ZAL2m), are therefore of potential interest toward understanding the molecular underpinnings of these phenotypes. To identify genes that are differentially expressed between the two morphs and correlated with behavior, we quantified both behavior and gene expression in a population of free-living white-throated sparrows. We quantified behavioral responses to simulated territorial intrusions (STIs) early during the breeding season. In the same birds, we then performed a transcriptomewide analysis of gene expression in two behaviorally relevant brain regions, the medial amygdala and hypothalamus. Using network analyses, we identified modules of genes that were correlated with both morph and STI-induced singing behavior. The majority of these genes were located within the inversion, demonstrating the profound effect the inversion has on the expression of genes captured by the rearrangement. Gene pathway analyses revealed that in the medial amygdala, the most prominent pathways were those related to steroid hormone receptor activity. Within these pathways, the only gene encoding such a receptor was ESR1 (estrogen receptor alpha). Our results thus suggest that ESR1 and related genes are important for behavioral differences between the morphs. Overall design: RNA samples from the brain regions HYP and MeA were collected from a total of 19 male white-throated sparrows (10 WS and 9 TS). Free-living birds were collected during the peak of territorial behavior (May-June) the day after a simulated territorial intrusion using mist nets and song playback. For the MeA samples, MeA constituted the majority of the sampled tissue. For the HYP, samples included the caudal portion of the medial preoptic area (POM), the paraventricular nucleus (PVN), the anterior hypothalamus, and the ventromedial hypothalamus (VMH).
Sample: Sample_23608_Hyp
SAMN04437838 • SRS1259848 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 1000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Brains were quickly removed and flash frozen on dry ice. Brains were cryosectioned at 300um thickness and regions of interest (HYP and MeA) regions were micro dissectied from frozen setions using a 1mm punch tool. A total of 4 punches were collected from each bird and region and were pooled for RNA extraction. RNA was extracted using the Qiagen Allprep DNA/RNA micro kit with modification, as follows. Punches were homogenized in RLT plus + β-mercaptoethanol using a pellet mixer. An equal volume of phenol:chloroform:isoamyl alcohol (25:24:1) pH 7.5 was added to each sample. Samples were further homogenized by passing them through a Qiashredder column (Qiagen). Phases were separated by spinning for 15 min at 4°C, and the aqueous phase was collected and further processed according to the manufacturer’s protocol. Libraries were prepped using Illumina TruSeq RNA Sample Preparation Kit v2. Libraries were constructed using 250 ng total RNA.
Experiment attributes:
GEO Accession: GSM2045649
Links:
Runs: 1 run, 15.3M spots, 3.1G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR311539215,285,4453.1G1.8Gb2017-11-15

ID:
2186549

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