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SRX26083795: GSM8516057: Xenopus embryo, stage 35, 0.1X MMR, sample 3; Xenopus laevis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 14M spots, 1.1G bases, 447.2Mb downloads

External Id: GSM8516057_r1
Submitted by: Levin lab, Biology, Tufts University
Study: Xenobot Transcriptomics: Gene Expression Changes in wild-type cells forming one form of synthetic biobot
show Abstracthide Abstract
The standard paradigm of developmental and synthetic biology focuses on changes in morphology driven by gene expression. Here, we investigated the reverse relationship: would transcriptomes change if cell collectives acquired a novel morphogenetic and behavioral phenotype in the absence of genomic editing, transgenes, heterologous materials, or drugs? We investigated the effects of morphology and nascent emergent life history on gene expression in Xenobots – motile, autonomous constructs that self-assemble from frog embryo epidermal progenitor cells. We compared transcriptomes of Xenobots with age-matched frog embryos, identifying at least 537 transcripts uniquely upregulated in the Xenobots. Pathway analyses indicated shifts in the categories of motility machinery, pattern formation and multicellularity, stress and immune response, metabolism, and sensory perception of sound and mechanical stimuli. Phylostratigraphic analysis showed that the majority of these shifts in Xenobots were towards evolutionarily ancient transcripts and systems. Lastly, we found enrichment of thanatotranscriptomic genes, shedding light on the distinction between death of an organism and that of its cells. These data on the relationship between genotype and phenotype may have implications for evolution, biomedicine, and synthetic morphoengineering. Overall design: Comparative gene expression profiling analysis of RNA-seq data for Xenopus embryos raised in 0.1X MMR and 0.75X MMR. 0.1X MMR and 0.75X MMR Xenopus embryo embryo samples are in triplicates
Sample: Xenopus embryo, stage 35, 0.1X MMR, sample 3
SAMN43764488 • SRS22651095 • All experiments • All runs
Organism: Xenopus laevis
Library:
Name: GSM8516057
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Each sample (0.1X MMR and 0.75X MMR) of Xenopus embryos consisted of 10 pooled stage 35 Xenopus embryos and each was repeated 3 times. RNA was extracted using TRI Reagent (Molecular Research Center, Inc - MRC) as per the manufacturer's protocol, and total RNA quality and quantity was assessed using a NanoDrop spectrophotometer (Thermo Fisher Scientific). RNA library preparation was done with the Illumina Stranded Total RNA with Ribo-Zero Plus. Libraries were then multiplexed, and an rRNA depletion run using single-end, 75-nucleotide sequencing was performed on Illumina HiSeq 2500.
Runs: 1 run, 14M spots, 1.1G bases, 447.2Mb
Run# of Spots# of BasesSizePublished
SRR3066486314,044,4311.1G447.2Mb2024-09-20

ID:
35198190

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