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Status |
Public on Sep 28, 2017 |
Title |
Identification of AtGRP7 targets by RIP-seq |
Organism |
Arabidopsis thaliana |
Experiment type |
Other
|
Summary |
A key function for RNA-binding proteins in orchestrating plant development and environmental responses is well established. However, the lack of a genome-wide view on their in vivo binding targets and binding landscapes represents a gap in understanding the mode of action of plant RNA-binding proteins. Here, we conducted RNA Immunoprecipitation (RIP-seq) for genome-wide determining the binding repertoire of the circadian clock-regulated Arabidopsis thaliana glycine-rich RNA-binding protein AtGRP7.
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Overall design |
AtGRP7 RIP-seq
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Contributor(s) |
Meyer K, Köster T, Nolte C, Weinholdt C, Lewinski M, Grosse I, Staiger D |
Citation(s) |
29084609 |
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Submission date |
May 30, 2017 |
Last update date |
Oct 11, 2019 |
Contact name |
Martin Lewinski |
Organization name |
Bielefeld University
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Department |
RNA Biology and Molecular Physiology
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Street address |
Universitätsstraße 25
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City |
Bielefeld |
ZIP/Postal code |
33615 |
Country |
Germany |
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Platforms (1) |
GPL13222 |
Illumina HiSeq 2000 (Arabidopsis thaliana) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE99616 |
Adaptation of iCLIP to plants determines the binding landscape of the clock-regulated RNA-binding protein AtGRP7 |
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Relations |
BioProject |
PRJNA388502 |
SRA |
SRP108303 |