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ERX013225: Deep sequencing of rainbow trout male embryonic gonads using 454 GS FLX Titanium technology
1 LS454 (454 GS FLX Titanium) run: 413,634 spots, 228.2M bases, 501.2Mb downloads

Design: The Roche 454 Titanium technology was used to sequence cDNA libraries made from gonads of all-male (XY) embryos sampled at 35 days post fertilization (dpf), i.e., at the very beginning of the molecular sex differentiation period in order to search for genes specifically expressed during gonadal differentiation
Submitted by: INRA-SCRIBE
Study: Evidence for conservation of a novel master sex-determining gene in salmonids
show Abstracthide Abstract
Master sex determining genes governing genetic sex determination have only been characterized in a very few non-mammalian vertebrates species. Teleost fishes represent the largest group of vertebrates on earth and are known for their extreme diversity with regards to sex determination. Among teleosts, all salmonid species investigated so far have a genetically determined sex with a male heterogamety. However, the master sex determining gene governing this strict genetic control in salmonid is still unknown. Here we found a previously unknown Y-chromosome gene specifically expressed during testicular differentiation in rainbow trout. This gene (named sdY for Sexually Dimorphic on the Y) was characterized by next-generation sequencing of male and female embryonic gonads. Its encodes a protein that is only found in salmonids and displays similarities with the C terminal domain of IRF9, a member of the Interferon Regulatory Factor family. We also demonstrated that sdY is conserved as a male-specific genomic sequence in all salmonids. This wide conservation of sdY -linkage with the heterogametic sex of salmonids was rather unexpected as these species do not share any Y chromosome conserved synteny. Because of its wide Y-linked conservation in salmonids and its pattern of expression restricted to the differentiating testis, our results provide strong evidence that sdY is a conserved salmonid master sex determining gene.
Sample: Oncorhynchus mykiss
SAMEA1462629 • ERS034682 • All experiments • All runs
Library:
Name: 35_dpf_Male
Instrument: 454 GS FLX Titanium
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Gonads were sampled in 35 days post fertilization (dpf) embryos obtained from genetically all-male (XY) rainbow trout populations. RNA extraction was carried out using the MELT Total Nucleic Acid Isolation System (Applied Biosystems/Ambion). After cDNA synthesis and amplification using SMARTer PCR cDNA Synthesis (Takara Bio Europe/Clontech), cDNA was nebulisated and libraries were prepared using the GS DNA Library Preparation Kit according to manufacturer's recommendations (Roche Applied Science, Meylan, France). Final libraries were quantified with the SlingShot kit using the Fluidigm Digital Array and sequenced using the 454/Roche GS FLX Titanium chemistry (GS Titanium LV emPCR and sequencing kits) according to manufacturer's informations. Each sample was sequenced on one region of a two regions Picotiterplate.
Spot descriptor:
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Runs: 1 run, 413,634 spots, 228.2M bases, 501.2Mb
Run# of Spots# of BasesSizePublished
ERR034907413,634228.2M501.2Mb2012-06-23

ID:
196974

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