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Status |
Public on Jan 10, 2022 |
Title |
A Bacillus anthracis RNA binding protein post-transcriptionally regulates two component signaling through RNA turnover [RIP-Seq] |
Organism |
Bacillus anthracis |
Experiment type |
Expression profiling by high throughput sequencing Other
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Summary |
Formaldehyde cross-linking RNA immunoprecipitation coupled with illumina sequencing (fRIP-seq) was performed to pinpoint the direct RNA targets of KrrA using a FLAG-tagged KrrA construct that is driven by a constitutive promoter Plgt (pOS1.PlgtkrrA-FLAG).
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Overall design |
Two different growth conditions were implemented: LB and LB supplemented with ‘205. Two controls were included to ensure specificity: (i) a WT strain that does not harbor the FLAG-tagged KrrA construct as a nonspecific background control, and (ii) RNA extracted from WT cells harvested before immunoprecipitation, serving as an input RNA control.
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Contributor(s) |
Pi H, Skaar EP |
Citation(s) |
35314695 |
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Submission date |
Jan 07, 2022 |
Last update date |
Apr 19, 2022 |
Contact name |
Hualiang Pi |
E-mail(s) |
hualiangpi@gmail.com
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Organization name |
VUMC
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Street address |
1161 21st Avenue South
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City |
Nashville |
State/province |
TN |
ZIP/Postal code |
37232 |
Country |
USA |
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Platforms (1) |
GPL31186 |
Illumina NovaSeq 6000 (Bacillus anthracis) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE193212 |
A Bacillus anthracis RNA binding protein post-transcriptionally regulates two component signaling through RNA turnover |
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Relations |
BioProject |
PRJNA795438 |