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Series GSE127247 Query DataSets for GSE127247
Status Public on Jan 17, 2020
Title Control of noncoding RNA production and histone levels by a 5’ tRNA fragment
Organisms Homo sapiens; Mus musculus
Experiment type Expression profiling by high throughput sequencing
Methylation profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Other
Summary Small RNAs derived from mature tRNAs, referred to as tRNA fragments or “tRFs”, are an emerging class of regulatory RNAs with poorly understood functions in cellular regulation. We recently identified a role for one specific tRF – 5’ tRF-Gly-GCC, or tRF-GG – in repression of genes associated with the endogenous retroelement MERVL, but the mechanistic basis for this regulation was unknown. Here, we show that tRF-GG plays a role in production of a wide variety of noncoding RNAs normally synthesized in Cajal bodies. Among these noncoding RNAs, tRF-GG regulation of the U7 snRNA modulates heterochromatin-mediated transcriptional repression of MERVL elements by supporting an adequate supply of histone proteins. Importantly, the effects of inhibiting tRF-GG on histone mRNA levels, activity of a histone 3’ UTR reporter, and ultimately on MERVL regulation could all be suppressed by the U7 RNA. We show that the related RNA-binding proteins hnRNPF and H bind directly to tRF-GG, and are required for Cajal body biogenesis. Together, our data reveal a conserved mechanism for 5’ tRNA fragment control of noncoding RNA biogenesis and, consequently, in global chromatin organization.
 
Overall design Mouse embryonic stem cells were transfected with tRNA fragments, LNA sequences against tRNA fragments, snRNAs, or siRNAs. Changes in gene expression were quantified using RNAseq and metabolic labeling. Changes in ribosomal rRNA methylation were quantified using Ribomethseq. Changes in chromatin architecture were probed with ATAC-seq. E14 mESCs were transfected with LNA-containing oligos antisense to tRF-GG or Mock transfected. iClip libraries were constructed against hnRNPF/H using sc-32310 antibody, with protocol from Zarnegar et al. 2016 Nat Methods.
 
Contributor(s) Bing XY, Rando OJ
Citation(s) 31831626, 32122968
Submission date Feb 27, 2019
Last update date Mar 23, 2020
Contact name Mike Levine
E-mail(s) msl2@princeton.edu
Organization name Princeton University
Department Lewis Sigler Institute
Street address South Dr
City Princeton
State/province NJ
ZIP/Postal code 08540
Country USA
 
Platforms (2)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (48)
GSM3633045 mESCs_siC1
GSM3633046 mESCs_siC2
GSM3633047 mESCs_siC3
Relations
BioProject PRJNA524479
SRA SRP186998

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
GSE127247_All_Ribomethseq_replicates_coverage.xlsx 3.0 Mb (ftp)(http) XLSX
GSE127247_All_peaks_compiled.xlsx 17.0 Mb (ftp)(http) XLSX
GSE127247_Boskovic_Table_S1.xlsx 3.5 Mb (ftp)(http) XLSX
GSE127247_Boskovic_Table_S2.xlsx 2.1 Mb (ftp)(http) XLSX
GSE127247_Boskovic_Table_S4.xlsx 2.2 Mb (ftp)(http) XLSX
GSE127247_tRFGG_Mock_24_1kb.bed.gz 19.7 Mb (ftp)(http) BED
GSE127247_tRFGG_Mock_48_10kb.bed.gz 2.0 Mb (ftp)(http) BED
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Processed data are available on Series record

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