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SRX4870852: GSM3427173: PreIPSN_V4; Mus musculus; RNA-Seq
3 ILLUMINA (Illumina HiSeq 3000) runs: 27.3M spots, 1.4G bases, 473.7Mb downloads

Submitted by: NCBI (GEO)
Study: The differences in local translatome across distinct neuron types is mediated by both baseline cellular differences and post-transcriptional mechanisms
show Abstracthide Abstract
Local translation in neurites is a phenomenon that enhances spatial segregation of proteins and their functions away from the cell body, yet it is unclear how local translation varies across neuronal cell types. Further, it is unclear if differences in local translation across cell types simply reflect differences in transcription or if there is also a cell type specific posttranscriptional regulation of the location and translation of specific mRNAs. Most of the mRNAs discovered as locally translated have been identified from hippocampal neurons because their laminar organization facilitates neurite specific dissection and microscopy methods. Given the diversity of neurons across the brain, studies have not yet analyzed how locally translated mRNAs differ across cell types, particularly those with neurites intertwined into other cell types. Here, we used the SynapTRAP method to harvest two broad cell types in the forebrain: GABAergic neurons and pyramidal neurons. While some transcripts overlap, the majority of the local translatome is not shared across these cell types. While most differences are driven by baseline expression levels in the respective cells, some transcripts also evidence cell type specific post transcriptional regulation of localization. Finally, we provide evidence that GABAergic neurons specifically localize mRNAs for peptide neurotransmitters, including somatostatin and cortistatin, suggesting localized production of these key signaling molecules in the neurites of GABAergic neurons. Overall, this work suggests that differences in local translation in neurites across neuronal cell types are poised to contribute substantially to the variability between cells. Overall design: 5 Replicates of 4 sample types, collect from two cell types each in the brain.
Sample: PreIPSN_V4
SAMN10234714 • SRS3925842 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina HiSeq 3000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Five replicates of RBP4-TRAP and VGAT-TRAP were harvested by rapid forebrain dissection at 21 days post birth as described (Ouwenga et al. 2017; Westmark et al. 2011). Each replicate contained a pool of two to three forebrains of both sexes as available. Four samples were collected from each replicate in parallel: whole cell homogenate (WCH) was RNA isolated from an aliquot of the initial homogenization of the tissue, TRAP was the capture of GFP-tagged ribosomes from an aliquot of WCH. RNA isolated from a fraction of the WCH subjected to synaptoneurosomal fractionation (SNF), and SynapTRAP (ST) is TRAP performed on the SNF, as described (Ouwenga et al. 2017). RNA concentration for all was measured using a Nanodrop and diluted to <5ng/µL before being assessed for quality and concentration using an Agilent TapeStation 4200 Library preparation was performed with 30ng of total RNA from each sample. ds-cDNA was prepared using the SMARTer Ultra Low RNA kit for Illumina Sequencing (Clontech #634936) per manufacturer's protocol. cDNA was fragmented using a Covaris E220 sonicator using peak incident power 18, duty factor 20%, cycles/burst 50, time 120 seconds at 18 degrees. cDNA was blunt ended, had an A base added to the 3'ends, and then had Illumina sequencing adapters ligated to the ends. Ligated fragments were then amplified for 13 cycles using primers incorporating unique index tags.
Experiment attributes:
GEO Accession: GSM3427173
Links:
Runs: 3 runs, 27.3M spots, 1.4G bases, 473.7Mb
Run# of Spots# of BasesSizePublished
SRR80402719,098,389454.9M157.7Mb2018-10-15
SRR80402729,020,375451M157.5Mb2018-10-15
SRR80402739,180,073459M158.5Mb2018-10-15

ID:
6571016

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