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SRX288475: GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER
9 ILLUMINA (Illumina HiSeq 2000) runs: 35.9M spots, 2.7G bases, 1.7Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition
show Abstracthide Abstract
Upon fertilization, maternal factors direct development in a transcriptionally silent embryo. At the maternal-to-zygotic transition (MZT), a universal step in animal development, unknown maternal factors trigger zygotic genome activation (ZGA). In zebrafish, ZGA is required for gastrulation and clearance of maternal mRNAs, which is achieved in part by the conserved microRNA miR-430. However, the precise factors that activate the zygotic program remain largely unknown. Here we show that Nanog, Pou5f1 and SoxB1 are required for genome activation in zebrafish. We identified several hundred genes directly activated by maternal factors, thus constituting the first wave of zygotic transcription in zebrafish. Ribosome profiling in the pre-MZT embryo revealed that nanog, sox19b and pou5f1 are the most highly translated transcription factor mRNAs. Combined loss of function for Nanog, SoxB1 and Pou5f1 resulted in developmental arrest prior to gastrulation, and a failure to activate >75% of zygotic genes. Furthermore, we found that Nanog binds the miR-430 locus and together with Pou5f1 and SoxB1 initiate miR-430 expression and activity. Our results demonstrate that maternal Nanog, Pou5f1 and SoxB1 are required to initiate the zygotic developmental program and in turn trigger the clearance of the maternal program by activating miR-430 expression. Overall design: Wild type and loss-of-function total mRNA sequencing of embryonic transcriptomes pre- and post-MZT; ribosome profiling pre-MZT
Sample: WT ribosome protected fragments for Ribosome Profiling
SAMN02183599 • SRS431102 • All experiments • All runs
Organism: Danio rerio
Library:
Instrument: Illumina HiSeq 2000
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: SINGLE
Construction protocol: For mRNA-Seq, total RNA from five embryos was extracted using Trizol (Invitrogen) for each experimental condition. RNA was treated with TURBO DNase (Ambion) for 30 minutes at 37°C and extracted using phenol chloroform. For ribosome profiling, 50 wild type embryos for each condition were collected at 64-cell stage. Embryos were lysed using 800ul of a mammalian cell lysis buffer containing 100ug/ml Cycloheximide as per the manufacturer’s instruction (ARTseq Ribosome Profiling Kit, RPHMR12126, Epicentre). For nuclease treatment, 3ul of ARTseq Nuclease was used. Ribosome protected fragments were run and 28-29nt fragments were gel purified as previously described in (Bazzini et al., 2012) and cloned according to the manufacturers protocol (ARTseq Ribosome Profiling Kit, RPHMR12126, Epicentre). TruSeq strand-specific libraries were constructed according to standard protocols. For total mRNA-Seq, sequencing libraries were treated with Epicentre Ribo-Zero Gold kits according to the published protocol, in order to deplete ribosomal RNA prior to sequencing. Ribosome profiling libraries were constructed as in (Bazzini et al., Science 2012).
Experiment attributes:
GEO Accession: GSM1152437
Links:
External link:
Runs: 9 runs, 35.9M spots, 2.7G bases, 1.7Gb
Run# of Spots# of BasesSizePublished
SRR8707254,000,000304M188Mb2013-09-23
SRR8707264,000,000304M194.3Mb2013-09-23
SRR8707274,000,000304M185.7Mb2013-09-23
SRR8707283,877,037294.7M190.5Mb2013-09-23
SRR8707294,000,000304M187.2Mb2013-09-23
SRR8707304,000,000304M190.3Mb2013-09-23
SRR8707314,000,000304M191.4Mb2013-09-23
SRR8707324,000,000304M183.1Mb2013-09-23
SRR8707334,000,000304M187.4Mb2013-09-23

ID:
408310

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