keywords: |
Transcriptome or Gene expression
|
ID: |
PRJNA138951
|
description: |
Exon and expression analysis of HeLa cells after knockdown of SON
Serine-arginine-rich (SR) proteins play a key role in alternative pre-mRNA splicing in eukaryotes. Our laboratory recently showed that a large SR protein called Son has unique repeat motifs that are essential for maintaining the subnuclear organization of pre-mRNA processing factors in nuclear speckles. Motif analysis of Son highlights putative RNA interaction domains that suggest a direct role for Son in pre-mRNA splicing. A genome-wide screen was performed to identify putative human transcription and splicing targets of Son.
Overall design: HeLa cells were transfected with siRNA against SON or a control siRNA (siLuciferase) for 48 hours. Five biological replicates were used for each condition.
|
accesstypes: |
download
|
landingpage: | http://www.ncbi.nlm.nih.gov/bioproject/PRJNA138951 |
authentication: |
none
|
authorization: |
none
|
ID: |
pmid:22193954
|
name: |
Homo sapiens
|
ncbiID: |
ncbitax:9606
|
abbreviation: |
NCBI
|
homePage: | http://www.ncbi.nlm.nih.gov |
ID: |
SCR:006472
|
name: |
National Center for Biotechnology Information
|
homePage: | http://www.ncbi.nlm.nih.gov/bioproject |
ID: |
SCR:004801
|
name: |
NCBI BioProject
|
Nonsense-mediated decay of alternative precursor mRNA splicing variants is ...
A Quantitative, High-Throughput Reverse Genetic Screen Reveals Novel Connec...
Differential Recruitment of the Splicing Machinery during Transcription Pre...
Polypyrimidine tract-binding protein homologues from Arabidopsis are key re...
Functional splicing network reveals extensive regulatory plasticity of the ...