NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE124554 Query DataSets for GSE124554
Status Public on Feb 04, 2019
Title Axonogenesis is coordinated by alternative splicing programming and splicing regulator PTBP2
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary How a neuron acquires an axon is a fundamental question. Piecemeal identification of many axonogenesis-related genes has been done, but coordinated regulation is unknown. Through unbiased transcriptome profiling of immature primary cortical neurons during early axon formation, we discovered an association between axonogenesis and neuron-specific alternative splicing. Known axonogenesis genes exhibit little expression alternation but widespread splicing changes. Axonogenesis-associated splicing is governed by RNA binding protein PTBP2, which is enriched in neurons and peaks around axonogenesis in the brain. Cortical depletion of PTBP2 prematurely induces axonogenesis-associated splicing, causes imbalanced expression of axonogenesis-associated isoforms, and specifically affects axon formation in vitro and in vivo. PTBP2-controlled axongeneisis-associated Shtn1 splicing determines SHTN1’s capacity to regulate actin interaction, polymerization, and axon growth. Precocious Shtn1 isoform switch contributes to disorganized axon formation of Ptbp2-/- neurons. We conclude that PTBP2-orchestrated alternative splicing programming is required for robust generation of a single axon in mammals.
 
Overall design Immature cortical neurons were cultured from embryonic day 14 mouse neocortices at the density of 1 million cells per 35 mm petri dish. At 1 day in vitro (1 DIV), these neurons extend multiple indistinguishable processes in a seemingly random manner, just like pre-axonogenesis neurons in vivo. Around 3 DIV, one of the neurites accelerates its growth to become the axon. We performed unbiased deep RNA sequencing (RNA-Seq) of wildytpe DIV 1, wildtype DIV 3, and Ptbp2-/- DIV1 neurons. There are two biological replicates per sample (specific gentoype and age).
 
Contributor(s) Zheng S, Chen L
Citation(s) 30733148
Submission date Jan 02, 2019
Last update date May 06, 2019
Contact name Liang Chen
Organization name University of Southern California
Street address 1050 Childs Way
City Los Angeles
State/province CA
ZIP/Postal code 90089
Country USA
 
Platforms (1)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (6)
GSM3536443 DIV1_WT_1
GSM3536444 DIV1_WT_2
GSM3536445 DIV3_WT_1
Relations
BioProject PRJNA512484
SRA SRP175008

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
GSE124554_Gene_RSEM_cnt.xlsx 2.1 Mb (ftp)(http) XLSX
GSE124554_Transcript_RSEM_cnt.xlsx 5.6 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap