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Status |
Public on Jan 01, 2010 |
Title |
Expression from C. elegans L4 animals |
Organism |
Caenorhabditis elegans |
Experiment type |
Expression profiling by array
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Summary |
Nutrient-driven O-GlcNAcylation of key components of the transcription machinery may epigenetically modulate gene expression in metazoans. Knockouts of the O-GlcNAc cycling enzymes in C. elegans are viable and fertile, allowing a global analysis of the impact of GlcNAcylation. Whole genome transcriptional profiling of the O-GlcNAc cycling mutants confirmed dramatic deregulation of genes in these key pathways. As predicted, the O-GlcNAc cycling mutants show phenotypically altered lifespan and susceptibility to UV stress.
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Overall design |
Similarly aged L4 animals (20) staged by degree of vulval development were hand picked. Wild type and mutant animals were collected and total RNA isolated for gene expression analysis
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Contributor(s) |
Krause M, Hanover J |
Citation(s) |
20368426, 30250452 |
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Submission date |
Sep 16, 2009 |
Last update date |
Jun 11, 2019 |
Contact name |
Michael Krause |
E-mail(s) |
mwkrause@helix.nih.gov
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Phone |
(301) 402-4633
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Organization name |
NIH
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Department |
LMB/NIDDK
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Lab |
Krause
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Street address |
5 Center Drive
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
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Platforms (1) |
GPL200 |
[Celegans] Affymetrix C. elegans Genome Array |
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Samples (9)
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This SubSeries is part of SuperSeries: |
GSE18132 |
Dynamic O-GlcNAc cycling at promoters of C. elegans genes regulating Longevity, Stress, and Immunity |
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Relations |
BioProject |
PRJNA123477 |
Supplementary file |
Size |
Download |
File type/resource |
GSE18131_RAW.tar |
64.8 Mb |
(http)(custom) |
TAR (of CEL, CHP) |
Processed data included within Sample table |
Processed data provided as supplementary file |
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