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Series GSE35842 Query DataSets for GSE35842
Status Public on Dec 01, 2013
Title RIP-seq analysis of eukaryotic Sm proteins identifies three major categories of Sm-containing ribonucleoproteins
Organisms Drosophila melanogaster; Homo sapiens
Experiment type Non-coding RNA profiling by high throughput sequencing
Expression profiling by high throughput sequencing
Summary Background: Sm proteins are multimeric RNA-binding factors, found in all three domains of life. Eukaryotic Sm proteins, together with their associated RNAs, form small ribonucleoprotein (RNP) complexes important in multiple aspects of gene regulation. Comprehensive knowledge of the RNA components of Sm RNPs is critical for understanding their functions.
Results: We developed a multi-targeting RNA-immunoprecipitation sequencing (RIP-seq) strategy to reliably identify Sm-associated RNAs from Drosophila ovaries and cultured human cells. Using this method, we discovered three major categories of Sm-associated transcripts: small nuclear (sn)RNAs, small Cajal body (sca)RNAs and mRNAs. Additional RIP-PCR analysis showed both ubiquitous and tissue-specific interactions. We provide evidence that the mRNA-Sm interactions are mediated by snRNPs, and that one of the mechanisms of interaction is via base pairing. Moreover, the Sm-associated mRNAs are mature, indicating a splicing-independent function for Sm RNPs.
Conclusions: This study represents the first comprehensive analysis of eukaryotic Sm-containing RNPs, and provides a basis for additional functional analyses of Sm proteins and their associated snRNPs outside of the context of pre-mRNA splicing. Our findings expand the repertoire of eukaryotic Sm-containing RNPs and suggest new functions for snRNPs in mRNA metabolism.
 
Overall design RNA-Immunoprecipitation sequencing of RNA-Sm protein complexes.
 
Contributor(s) Lu Z, Guan X, Schmidt CA, Matera AG
Citation(s) 24393626
Submission date Feb 15, 2012
Last update date May 15, 2019
Contact name Zhipeng Lu
E-mail(s) zhipengluchina@gmail.com
Organization name Stanford University
Department Department of Dermatology
Lab Howard Chang
Street address 269 Campus Drive
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
Platforms (2)
GPL9061 Illumina Genome Analyzer II (Drosophila melanogaster)
GPL9115 Illumina Genome Analyzer II (Homo sapiens)
Samples (28)
GSM876115 Lu001
GSM876116 Lu002
GSM876117 Lu003
Relations
SRA SRP010944
BioProject PRJNA151853

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Supplementary file Size Download File type/resource
GSE35842_RAW.tar 479.7 Mb (http)(custom) TAR (of BEDGRAPH, RPKM, TXT, WIG)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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