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SRX5001244: GSM3466662: ATAC-Seq WT ZT16 rep1 rep2; Danaus plexippus; ATAC-seq
2 ILLUMINA (Illumina HiSeq 2500) runs: 34M spots, 1.7G bases, 803Mb downloads

Submitted by: NCBI (GEO)
Study: Genome-wide discovery of daily transcriptome, cis-regulatory elements and transcription factor footprints in the monarch butterfly brain [ATAC-Seq]
show Abstracthide Abstract
The Eastern North American monarch butterfly, Danaus plexippus, is notorious for its spectacular seasonal long-distance migration. In recent years, it has also emerged as a novel system to study how animal circadian clocks keep track of time and regulate ecologically relevant daily rhythmic activities and seasonal behavioral outputs. However, unlike Drosophila and the mouse, little work has been undertaken in the monarch to identify clock-controlled output genes and elucidate the regulation of their rhythmic expression. Here, we used RNA-sequencing and Assay for Transposase-Accessible Chromatin (ATAC)-sequencing to profile the diurnal transcriptome, open chromatin regions, and transcription factor (TF) footprints in the brain of wild-type monarchs and Cryptochrome 2 (Cry2), Clock (Clk), and Bmal1 (named DCyc-like) butterfly mutants with impaired clock function. We identified 366 rhythmic transcripts under circadian clock control belonging to biological processes key to brain function, such as neurotransmission, neuropeptide signaling, and glucose metabolism. Surprisingly, we found no significant time of day and genotype-dependent changes in chromatin accessibility (i.e., cis-regulatory elements) in the brain. Instead, we found the existence of a temporal regulation of TFs occupancy within open chromatin regions in the vicinity of rhythmic genes in the brains of wild-type monarchs, which is abolished in clock deficient mutants. Our data suggest that TFs binding specifically in the middle of the day display pioneer-like activity by increasing the accessibility of the surrounding chromatin, while TFs binding specifically in the middle of the night would bind DNA with a longer residency time without affecting accessibility of the surrounding chromatin. Together, this work identifies for the first time the clock-controlled genes and modes of regulation by which diurnal transcription rhythms are regulated in the monarch brain. It also illustrates the power of ATAC-seq to profile genome-wide regulatory elements and TF binding in unconventional organisms. Overall design: Determine the identify of clock-controlled genes and their cis-regulatory elements in monarch butterfly brains using RNA-Seq and ATAC-Seq open chromatin profiling.
Sample: ATAC-Seq WT ZT16 rep1 rep2
SAMN10413461 • SRS4035960 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: ATAC-seq
Source: GENOMIC
Selection: other
Layout: SINGLE
Construction protocol: Brains free of eye photoreceptors were dissected in ice-cold ringer's solution and resuspended twice in 600 μl of NP-40 lysis buffer (10mM Tris-HCl at pH 7.5, 10mM NaCl, 3 mM MgCl2, and 0.1% NP-40). Crude nuclei were prepared by homogenizing the brains in a 2 ml, ice-cold, Dounce homogenizer with two strokes of a loose-fitting pestle. Nuclei was directly subjected to transposition by Tn5 transposase for 30 min at 37°C using the Nextera DNA Library Preparation Kit (Illumina), and the tagmented DNA was then purified using a Zymo DNA Clean & ConcentratorTM-5 Kit, all according to a previously published protocol (Buenrostro et al, 2015). To generate a control naked DNA library, 1ng of genomic DNA extracted with phenol/chloroform was also subjected to transposition by Tn5 transposase and the tagmented DNA was purified following the same procedures. Barcoded libraries were PCR amplified, each using a common custom primer and a unique custom Nextera barcoded primer, as in (Buenrostro et al, 2015). For each library, after an initial round of five PCR cycles, the optimal number of PCR cycles to stop amplification prior to saturation was estimated by real-time quantitative PCR. Five to ten additional PCR cycles were then performed bringing the total number to 10 (for control DNA) to 15 cycles, and the libraries were purified using a Qiagen MinElute PCR purification kit. Libraries quality and size distribution was assessed on a Bioanalyzer, libraries were quantified by real-time quantitative PCR and mixed in equimolar ratios before sequencing on a single lane of using 50bp single end reads on an Hi-seq 2500 (Illumina).
Experiment attributes:
GEO Accession: GSM3466662
Links:
Runs: 2 runs, 34M spots, 1.7G bases, 803Mb
Run# of Spots# of BasesSizePublished
SRR818124317,533,260876.7M414.7Mb2019-07-02
SRR818124416,441,572822.1M388.3Mb2019-07-02

ID:
6743798

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