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SRX4525915: GSM3326045: Kwon201408_XenopusHybrid_TETS1; Xenopus tropicalis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 36.2M spots, 7.3G bases, 3.4Gb downloads

Submitted by: NCBI (GEO)
Study: Xenopus hybrids provide insight into cell and organism size control
show Abstracthide Abstract
Determining how size is controlled is a fundamental question in biology that is poorly understood at the organismal, cellular and subcellular levels. The Xenopus species, X. laevis and X. tropicalis differ in size at all three of these levels. Despite these differences, fertilization of X. laevis eggs with X. tropicalis sperm gives rise to viable hybrid animals that are intermediate in size. Hybrid and X. laevis embryos initially start from the same size egg and develop at the same rate, but hybrid animals were smaller by the tailbud stage, and reduced nuclear to cell size ratios were observed shortly after zygotic genome activation (ZGA), indicating that differential gene expression may contribute to size differences. Transcriptome analysis at the onset of ZGA identified twelve transcription factors paternally expressed in hybrids. A screen of these X. tropicalis factors by expression in X. laevis embryos revealed that Hes7 and Ventx2 were sufficient to significantly reduce X. laevis organismal size by the tailbud stage, although nuclear to cell size ratios were not significantly affected. Together, these results suggest that transcriptional regulation contributes to biological size control in Xenopus. Overall design: Collect mRNA from whole embryos; three biological replicates were analyzed
Sample: Kwon201408_XenopusHybrid_TETS1
SAMN09788949 • SRS3643905 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: To isolate RNA, embryos at stage 9 were homogenized mechanically in TRIzol® (Thermo Fisher Scientific, Waltham, MA) using up to a 30-gauge needle and processed according to manufacturer instructions. After resuspension in nuclease-free H2O, RNAs were cleaned using a RNeasy kit (Qiagen Inc.) according to manufacturer instructions. Libraries were prepared using manufacturer's non-standard specific RNA-seq library protocol with poly-A capturing mRNA enrichment method (Illumina, CA, USA)
Experiment attributes:
GEO Accession: GSM3326045
Links:
Runs: 1 run, 36.2M spots, 7.3G bases, 3.4Gb
Run# of Spots# of BasesSizePublished
SRR766534736,197,6427.3G3.4Gb2018-12-21

ID:
6130455

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