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SRX9246289: N. vectensis RNA-Seq Blastula 2
1 ILLUMINA (Illumina HiSeq 2000) run: 47.6M spots, 9.6G bases, 5.9Gb downloads

Design: Developmental and adult N. vectensis RNA sequencing was performed as follows. N. vectensis were spawned and eggs were de-jellied and fertilized as previously described. Spawning and embryo development took place at 18 C. Eggs and embryos from different stages were collected (300 per sample) in duplicate as indicated: eggs (within 30min of spawn), blastula (7.5hpf), gastrula (23.5hpf) and planula (72hpf). Eggs and embryos were collected in eppendorf tubes and centrifuged to a pellet at 21,000 x g for 1 min. All seawater was quickly removed and pellets were resuspended in 150ml lysis buffer (RLT buffer supplied by the Qiagen RNeasy kit (#74104), supplemented with -mercaptoethanol). The samples were homogenized with an electric pestle (1 min continuous drilling) and further supplemented with 200 ml of the above lysis buffer. Homogenized samples were then transferred into QIAshredder columns (Qiagen #79654) and centrifuged at 21,000 x g for 2 min. The flow throughs were supplemented with 1 ml 70 % ethanol and transferred to RNeasy columns and were processed according to the Qiagen RNeasy protocol. Quality and integrity of the RNA was evaluated using the Agilent RNA 600 pico kit (Agilent Technologies) and RNA samples were stored at -80 C until further processing. cDNA libraries were then constructed for polyA stranded sequencing. The resulting libraries were sequenced on Illumina HiSeq using paired end runs (RapidSeq- 2x150bp).
Submitted by: University of Vienna
Study: Edwardsiid Genomes
show Abstracthide Abstract
Cnidaria (sea anemones, jellyfish, corals and hydra) form a close outgroup to Bilateria, and the sea anemone Nematostella vectensis has emerged as a slow evolving model, illuminating characteristics of the most recent common ancestor to Bilateria, which diverged near the Cambrian explosion. Using long read sequencing and high throughput chromosome conformation capture, we generated high quality chromosome-level assemblies of N. vectensis and the closely related edwardsiid sea anemone, Scolanthus callimorphus. In both cases we find a robust set of 15 chromosomes comprising a stable linkage group detectable within all major clades of sequenced cnidarian genomes and demonstrate remarkable chromosomal conservation with chordates. Unlike in Bilateria, extended Hox and NK gene clusters are chromosomally linked but do not retain a tight spatial conservation. Accordingly, we also observe a lack of evidence for topologically associated domains, which have been implicated in the evolutionary pressure to retain tight microsyntenic gene clusters. We also uncover ultra-conserved noncoding elements at levels previously undetected in non-chordate lineages. Both genomes are accessible through an actively updated genome browser and database at https://simrbase.stowers.org.
Sample: Nematostella vectensis blastula for RNA-Seq 2
SAMN16376581 • SRS7478946 • All experiments • All runs
Library:
Name: L3711
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Runs: 1 run, 47.6M spots, 9.6G bases, 5.9Gb
Run# of Spots# of BasesSizePublished
SRR1277598147,593,3099.6G5.9Gb2021-04-20

ID:
12063516

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