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Status |
Public on Jun 20, 2014 |
Title |
Analysis of the expression of Ataxin-2-target genes |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
We recently identified the RNA targets of Ataxin-2 by using PAR-CLIP. To elucidate the functional role of Ataxin-2 on target-binding, we have knocked down or overexpressed Ataxin-2 in HEK293T cells and extracted RNAs 48 hrs after transfection. Then, these total RNAs were subjected to whole transcripts microarray analysis to examine how the perturbation of Ataxin-2 expression affects target gene expression.
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Overall design |
Ataxin-2 was either knocked down using siRNA or overexpressed using the expression construct of Halo-Ataxin-2.Control siRNA was transfected as a control of knockdown experiment. The expression construct of Halo-tag alone was used as a control of overexpression experiment. Forty-eight hrs after transfection, total RNAs were extracted and subjected to microarray analysis.
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Contributor(s) |
Yamamoto M, Yokoshi M, Kawahara Y |
Citation(s) |
24954906 |
Submission date |
Dec 10, 2013 |
Last update date |
Jan 09, 2018 |
Contact name |
Yukio Kawahara |
E-mail(s) |
ykawahara@rna.med.osaka-u.ac.jp
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Phone |
+81-6-6879-3827
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Organization name |
Osaka University
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Department |
Graduate School of Medicine
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Lab |
Laboratory of RNA Function
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Street address |
2-2 Yamada-oka
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City |
Suita |
State/province |
Osaka |
ZIP/Postal code |
565-0871 |
Country |
Japan |
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Platforms (1) |
GPL17077 |
Agilent-039494 SurePrint G3 Human GE v2 8x60K Microarray 039381 (Probe Name version) |
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Samples (12)
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Relations |
BioProject |
PRJNA231072 |