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SRX3316197: GSM2829092: heart / ferret; Mustela putorius furo; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 29.4M spots, 5.9G bases, 3.5Gb downloads

Submitted by: NCBI (GEO)
Study: A quantitative model for characterizing the evolutionary history of mammalian gene expression
show Abstracthide Abstract
Characterizing the evolutionary history of a gene's expression profile is a critical component for understanding the relationship between genotype, expression, and phenotype. However, it is not well-established how best to distinguish the different evolutionary forces acting on gene expression. Here, we use RNA-seq across 7 tissues from 17 mammalian species to show that expression evolution across mammals is accurately modeled by the Ornstein-Uhlenbeck (OU) process. This stochastic process models expression trajectories across time as Gaussian distributions whose variance is parameterized by the rate of genetic drift and strength of stabilizing selection. We use these mathematical properties to identify expression pathways under neutral, stabilizing, and directional selection, quantify the extent of selective pressure on a gene's expression, and detect deleterious expression levels outside expected evolutionary distributions in single patients. Our work provides a statistical framework for interpreting expression data across species and in disease. Overall design: RNA-sequencing of 7 tissues (brain, heart, kidney, liver, lung, skeletal muscle, testis) from rabbit, dog, ferret, cow, armadillo, and opposum
Sample: heart / ferret
SAMN07828471 • SRS2621784 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: 10ug total RNA was poly-A selected twice using Dynabeads mRNA Purification Kit (Invitrogen, 610.06). Resulting mRNA was DNase treated (Ambion AM1907) and then fragmented using heat. First strand cDNA synthesis was performed using the SuperScript Double-Stranded cDNA Synthesis Kit (Invitrogen, 11917-010), supplementing in SuperScript III Reverse Transcriptase (Invitrogen, 18080-093), incorporating SUPERase*In (Ambion, AM2694), and Actinomycin D (USB, 10415). First strand cDNA was cleaned using 1.8x RNAClean XP SPRI beads (Beckman Coulter, A64987). Second-Strand Synthesis was performed replacing dTTP with dUTP, and the resulting double-stranded cDNA was cleaned using a MinElute PCR Purification Kit (Qiagen, 28004). Illumina libraries were constructed by repairing the ends of the cDNA, ligating adapters, and cleaning/size-selecting with 0.7x SPRI. Illumina libraries were treated with USER to excise dUTP, and amplified via PCR using Fusion Master mix with GC buffer (NEB, F532S). Samples were sequenced on HiSeq 2000 machines, to a minimum depth of 35 million reads.
Experiment attributes:
GEO Accession: GSM2829092
Links:
Runs: 1 run, 29.4M spots, 5.9G bases, 3.5Gb
Run# of Spots# of BasesSizePublished
SRR620690229,394,1305.9G3.5Gb2018-10-22

ID:
4644934

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