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SRX2254820: GSM2356636: 15hpa; Xenopus tropicalis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 179.7M spots, 36.3G bases, 23.8Gb downloads

Submitted by: NCBI (GEO)
Study: RNA-Seq of Xenopus tail regeneration
show Abstracthide Abstract
In contrast to humans, many amphibians are able to rapidly and completely regenerate complex tissues, including complete appendages. Following tail amputation, Xenopus tropicalis tadpoles quickly regenerate muscle, spinal cord, cartilage, vasculature and skin, all properly patterned in three dimensions. To better understand the molecular basis of this regenerative competence, we performed a transcriptional analysis of regeneration using RNA-Seq. We profiled the transcriptome at 6 timepoints during tail regeneration, and used clustering analysis to identify biological processes that are prioritized during different transitions in the regeneration process. Our work expands significantly on previous expression analyses of tail regeneration. We are able to refine the windows during which many key biological signaling processes act, including embryonic patterning signals, immune responses, bioelectrical signaling and apoptosis. By including multiple timepoints within the first 24 hours post-amputation, we have also identified new processes that are highly prioritized early in regeneration, including axonogenesis, chemotaxis, and RNA metabolism. Our work provides a deep database for researchers interested in appendage regeneration, and highlights new avenues for further study. Overall design: Whole tail (WT) samples were obtained from an an initial amputation. Immediately thereafter, a second amputation was performed on the cut tadpole to obtain 0 hour time point samples. The 0 hpa time point samples the tissue directly adjacent to the initial cut site. Regenerating tail samples collected up to 72 hpa. Expression profiling of six time points in tadpole tail regeneration were sequenced in duplicate via Illumina HiSeq.
Sample: 15hpa
SAMN05930350 • SRS1754388 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Tadpole tails were amputated and immediately placed in lysis buffer (1% SDS, 0.100M NaCl, 0.010M EDTA, 0.20M Tris ph 7.6, Proteinase K) followed by ethanol precipitation to extract RNA. Illumina TruSeq RNA Sample Prep Kit was used with 1 ug of total RNA for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM2356636
Links:
Runs: 1 run, 179.7M spots, 36.3G bases, 23.8Gb
Run# of Spots# of BasesSizePublished
SRR4435593179,698,38336.3G23.8Gb2017-01-30

ID:
3309978

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