Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling of C. elegans dcr-1, unc-32 homozygous mutants vs. coiling unc-32 (wild type) to investidate interference synthesis of small developmental RNAs


ABSTRACT: Homozygous mutant dcr-1 animals were analyzed by Affymetrix microarray analysis using whole worm adult animals. The worms was genetically marked with a recessive allele of unc-32 that exhibits a coiler phenotype in unc-32 homozygous null animals. The "wildtype" comparison worm used in this study were coiling unc-32 animals and the dcr-1 deficient animal contained both the dcr-1 and the unc-32 mutations. Worms were picked and pooled for analysis.
Wormbase concise description of dcr-1 (DiCer Related): The dcr-1 gene encodes a bidentate ribonuclease that is homologous to E. coli RNAse III; dcr-1 is required both for RNA interference and for synthesis of small developmental RNAs; DCR-1 interacts in vivo with RDE-4, a double-stranded RNA (dsRNA) binding protein required for RNAi that interacts with trigger dsRNAs and may function to deliver dsRNAs to DCR-1 for endonucleolytic processing.

ORGANISM(S): Caenorhabditis elegans

SUBMITTER: Brenda Bass 

PROVIDER: E-MEXP-957 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Genes misregulated in C. elegans deficient in Dicer, RDE-4, or RDE-1 are enriched for innate immunity genes.

Welker Noah C NC   Habig Jeffrey W JW   Bass Brenda L BL  

RNA (New York, N.Y.) 20070525 7


We describe the first microarray analysis of a whole animal containing a mutation in the Dicer gene. We used adult Caenorhabditis elegans and, to distinguish among different roles of Dicer, we also performed microarray analyses of animals with mutations in rde-4 and rde-1, which are involved in silencing by siRNA, but not miRNA. Surprisingly, we find that the X chromosome is greatly enriched for genes regulated by Dicer. Comparison of all three microarray data sets indicates the majority of Dice  ...[more]

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