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SRX336217: GSM686384: embryo_Shield_rep1; Danio rerio; ncRNA-Seq
1 ILLUMINA (Illumina Genome Analyzer II) run: 3.2M spots, 115.1M bases, 81.4Mb downloads

Submitted by: NCBI (GEO)
Study: Transcriptome-wide analysis of small RNA expression in early zebrafish development
show Abstracthide Abstract
During early vertebrate development, a large number of noncoding RNAs are maternally inherited or expressed upon activation of zygotic transcription. The exact identity, expression levels, and function during early vertebrate development for most of these noncoding RNAs remains largely unknown. miRNAs (microRNAs) and piRNAs (piwi-interacting RNAs) are two classes of small non-coding RNAs that play important roles in gene regulation during early embryonic development. Here, we utilized Illumina next generation sequencing technology to determine temporal expression patterns for both miRNAs and piRNAs during four distinct stages of early vertebrate development using zebrafish as a model system. For miRNAs, the expression patterns for 192 known miRNAs and 12 novel miRNAs within 123 different miRNA families were determined. Significant sequence variation was observed at the 5'' and 3'' ends of miRNAs with a large number of extra nucleotides added in a non-template directed manner. We also identified a large and diverse set of piRNAs expressed during early development, far beyond that expected if piRNA expression is restricted to germ cells. Our analyses represent the deepest investigation to date of small RNA expression during early vertebrate development and suggest important novel functions for small RNAs during embryogenesis. Overall design: Identify the expression of small RNAs in zebrafish embryos of four different developmental stages using high through-put sequencing
Sample: embryo_Shield_rep1
SAMN02196996 • SRS471211 • All experiments • All runs
Organism: Danio rerio
Library:
Instrument: Illumina Genome Analyzer II
Strategy: ncRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: Zebrafish embryos were collected at the 256-cell stage, sphere stage, shield stage, and 1dpf. Total RNA was isolated from embryos using Trizol. RNAs were fractionated on 15% denaturing polyacrylamide gels and small RNAs between 15-30 nucleotides were excised and purified. cDNA libraries were generated using specific linkers and RT/PCR, as previously described. Libraries were sequenced in the Genome Technology Core of Vanderbilt University using the Illumina sequencing platform.
Experiment attributes:
GEO Accession: GSM686384
Links:
Runs: 1 run, 3.2M spots, 115.1M bases, 81.4Mb
Run# of Spots# of BasesSizePublished
SRR9535763,196,331115.1M81.4Mb2015-07-22

ID:
472919

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