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Series GSE19054 Query DataSets for GSE19054
Status Public on Feb 17, 2010
Title Small RNA expression and strain specificity in the rat
Organism Rattus norvegicus
Experiment type Non-coding RNA profiling by high throughput sequencing
Summary Background Digital gene expression (DGE) profiling has become an established tool to study RNA expression. Here, we provide an in-depth analysis of small RNA DGE profiles from two different rat strains (BN-Lx and SHR) from six different rat tissues (spleen, liver, brain, testis, heart, kidney). We describe the expression patterns of known and novel micro (mi)RNAs and piwi-interacting (pi)RNAs. We confirmed the expression of 589 known miRNAs and identified 56 miRNAs homologous to known human or mouse miRNAs, as well as 45 new rat miRNAs. Furthermore, we confirmed specific A to I editing in brain for mir-376a/b/c and identified mir-377 as a novel editing target. In accordance with earlier findings, we observed a highly tissue-specific expression pattern for all tissues analyzed. The brain was found to express the highest number of tissue-specific miRNAs, followed by testis. Notably, our experiments also revealed robust strain-specific differential miRNA expression in the liver that is caused by genetic variation between the strains. Finally, we identified two types of germline-specific piRNAs in testis, mapping either to transposons or in strand-specific clusters. Taken together, the small RNA compendium described here advances the annotation of small RNAs in the rat genome. Strain and tissue-specific expression patterns furthermore provide a strong basis for studying the role of small RNAs in regulatory networks as well as biological process like physiology and neurobiology that are extensively studied in this model system.
 
Overall design Small RNAs from 6 tissues were cloned and sequenced. Tissues included whole brain, liver, spleen, heart, testis, kidney. Tissues were sequenced from 2 rats: one BN-Lx rat and one SHR rat. For strain-specific miRNA expression we included 4 replicate whole livers, i.e. from 2 BN-Lx rats and 2 SHR rats.
 
Contributor(s) Linsen SE, de Wit E, de Bruijn E, Cuppen E
Citation(s) 20403161
Submission date Nov 17, 2009
Last update date May 15, 2019
Contact name Sam Linsen
E-mail(s) s.linsen@hubrecht.eu
Phone +312121828
Organization name Hubrecht Institute
Department Genome Biology
Lab Cuppen lab
Street address Uppsalalaan 8
City Utrecht
ZIP/Postal code 3584CT
Country Netherlands
 
Platforms (1)
GPL9690 AB SOLiD System (Rattus norvegicus)
Samples (16)
GSM471497 BN-Lx_adult_male_whole_brain
GSM471498 BN-Lx_adult_male_whole_liver
GSM471499 BN-Lx_adult_male_whole_spleen
Relations
SRA SRP001897
BioProject PRJNA120555

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE19054_RAW.tar 280.0 Kb (http)(custom) TAR (of TXT)
GSE19054_README.txt.gz 552 b (ftp)(http) TXT
GSE19054_hairpins_rat.fa.gz 13.0 Kb (ftp)(http) FA
GSE19054_mature_6tissues.fa.gz 37.5 Kb (ftp)(http) FA
GSE19054_mature_liver_replicates.fa.gz 19.9 Kb (ftp)(http) FA
GSE19054_piRNA_clusters.txt.gz 3.6 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Processed data provided as supplementary file
Processed data are available on Series record
Raw data are available in SRA

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