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Status |
Public on Jan 01, 2014 |
Title |
Diversity of HrpL-regulons across Pseudomonas syringae isolates |
Organism |
Pseudomonas syringae |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
We implemented transcriptional analysis methods using cDNA and high-throughput sequencing data to identify HrpL-regulated genes for six strains of Pseudomonas syringae
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Overall design |
Each Pseudomonas syringae strains was transformed with either pBAD::EV or pBAD containing native hrpL sequence. Strains were grown in MM media supplemented with arabinose and collected 1, 3, and 5 hours post arabinose treatment. RNA was extracted for each time point and mixed at a 1/3 ratio. After removal of rRNA, double stranded cDNA was generated and library prepared accordeing to Illumina protocols.
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Contributor(s) |
Mucyn TS, Lind AL, Biswas S, Yoursatone S, Nishimura MT, Cumbie JS, Grant SR, Chang JH, Jones CD, Dangl JL |
Citation(s) |
24391493 |
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Submission date |
May 14, 2013 |
Last update date |
Aug 08, 2019 |
Contact name |
Emma Johnson |
E-mail(s) |
[email protected]
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Organization name |
University of North Carolina - Chapel Hill
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Department |
Biology
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Lab |
Dangl Lab
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Street address |
250 Bell Tower Dr
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City |
Chapel Hill |
State/province |
North Carolina |
ZIP/Postal code |
27599 |
Country |
USA |
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Platforms (2) |
GPL17159 |
Illumina Genome Analyzer II (Pseudomonas syringae) |
GPL17160 |
Illumina HiSeq 2000 (Pseudomonas syringae) |
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Samples (24)
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Relations |
BioProject |
PRJNA203106 |
SRA |
SRP022745 |