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Series GSE116164 Query DataSets for GSE116164
Status Public on Jun 23, 2018
Title Deficiency in SUMOylation, by injection of Gam1 mRNA into one cell embryos, leads to differential expression of genes in Xenopus
Organism Xenopus laevis
Experiment type Expression profiling by array
Summary Background: Adenovirus protein Gam1 triggers the proteolytic destruction of the E1 SUMO-activating enzyme. Microinjection of an empirically determined amount of Gam1 mRNA into one-cell Xenopus embryos can reduce SUMOylation activity to undetectable, but nonlethal levels, enabling an examination of the role of this post-translational modification during early vertebrate development.
Results: We find that SUMOylation-deficient embryos consistently exhibit defects in neural tube and heart development. We have measured differences in gene expression between control and embryos injected with Gam1 mRNA at three developmental stages: early gastrula (immediately following the initiation of zygotic transcription), late gastrula (completion of the formation of the three primary germ layers), and early neurula (appearance of the neural plate). Although changes in gene expression are widespread and can be linked to many biological processes, three pathways, non-canonical Wnt/PCP, snail/twist, and Ets-1, are especially sensitive to the loss of SUMOylation activity and can largely account for the predominant phenotypes of Gam1 embryos. SUMOylation appears to generate different pools of a given transcription factor having different specificities with this post-translational modification involved in the regulation of more complex as opposed to housekeeping processes.
Conclusions: We have identified changes in gene expression that underlie the neural tube and heart phenotypes resulting from depressed SUMOylation activity. Notably, these developmental defects correspond to the two most frequently occurring congenital birth defects in humans, strongly suggesting that perturbation of SUMOylation, either globally or of a specific protein, may frequently be the origin of these pathologies.
 
Overall design Three different time points (early gastrula-9 hours post fertilization, late gastrula- 13.5 hours post fertilization, and early neurula- 16.5 hours post fertilization). Twenty embryos from each time point. Three replicate experiments. Samples from control (injected with water) and experimental (injected with Gam1 mRNA).
 
Contributor(s) Bertke MM, Cronin L, Zeng E, Huber PW
Citation(s) 31101013
Submission date Jun 22, 2018
Last update date Jun 18, 2019
Contact name Paul Huber
E-mail(s) phuber@nd.edu
Organization name University of Notre Dame
Street address University of Notre Dame
City Notre Dame
State/province IN
ZIP/Postal code 46556
Country USA
 
Platforms (1)
GPL10756 [X_laevis_2] Affymetrix Xenopus laevis Genome 2.0 Array
Samples (18)
GSM3211707 Embryo at early gastrula, injected with 0.5ng Gam1 mRNA, biological replicate 1
GSM3211708 Embryo at early gastrula, injected with 0.5ng Gam1 mRNA, biological replicate 2
GSM3211709 Embryo at early gastrula, injected with 0.5ng Gam1 mRNA, biological replicate 3
Relations
BioProject PRJNA477522

Download family Format
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE116164_RAW.tar 64.4 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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