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RIP-CHIP data from CNOT6L WT and KO hepatocytes

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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE62365
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mRNA poly(A) tail plays a key role in post-transcriptional regulation of gene expression, including mRNA decay and translation. Deadenylation is a rate-limiting step in mRNA decay, which is catalyzed by the CCR4-NOT complex. To identify mRNAs associated with the CCR4-NOT complex, we have done RIP-CHIP (RNA-immunoprecipitation followed by DNA microarray) using primary hepatocytes from CNOT6L wild-type and knockout mice. Primary hepatocytes were isolated from 8-week-old wild-type and Cnot6l knockout (KO) mice. Each sample was divided into two parts for input RNA extraction, and anti-CNOT6L immunoprecipitation followed by RNA extraction. Input mRNA and immunoprecipitated (IPed) mRNA were hybridized to separate Mouse Genome 430 2.0 Affymetrix microarrays. Cnot6l KO hepatocytes was used as a negative control. All experiments were done in triplicates, with immunoprecipitated and input RNA from wild-type and CNOT6L KO hepatocytes generated for a total of 12 microarrays.
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2019-03-31
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