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Status |
Public on Apr 07, 2020 |
Title |
Cryptic introns in lncRNAs recruit conserved Pir2/ARS2 protein to promote gene repression [ChIP-seq] |
Organism |
Schizosaccharomyces pombe |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Long non-coding RNAs (lncRNAs) dynamically regulate gene expression during development and in response to environmental conditions. In S. pombe, lncRNAs repress the expression of nearby genes via a mechanism involving silencing effector proteins. In this study, we find that invasion of a lncRNA into the neighboring gene results in inclusion of a cryptic intron that is required for its repressive activity. We show that cryptic introns are targeted by the conserved protein Pir2/ARS2 in association with splicing factors, which provide a scaffold for the recruitment of RNA degradation factors and chromatin modifying activities.
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Overall design |
ChIP-seq of Pir2-GFP in Schizosaccharomyces pombe.
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Contributor(s) |
Thillainadesan G, Xiao H, Holla S, Dhakshnamoorthy J, Grewal SI |
Citation(s) |
32415063 |
Submission date |
Jul 31, 2019 |
Last update date |
Jun 08, 2020 |
Contact name |
Shiv Grewal |
Phone |
2407607553
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Organization name |
NCI
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Department |
LBMB
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Lab |
Shiv Grewal
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Street address |
NCI bldg 37 Rm 6068 9000 Rockville Pike
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
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Platforms (1) |
GPL20584 |
Illumina NextSeq 500 (Schizosaccharomyces pombe) |
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Samples (1) |
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This SubSeries is part of SuperSeries: |
GSE135161 |
Cryptic introns in lncRNAs recruit conserved Pir2/ARS2 protein to promote gene repression |
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Relations |
BioProject |
PRJNA557601 |
SRA |
SRP216891 |