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pmid:26097806

RNA-Seq analysis and whole genome DNA-binding profile of the Vibrio cholerae histone-like nucleoid structuring protein (H-NS).

Julio C Ayala · Hongxia Wang · Jorge A Benitez · Anisia J Silva

Genomics data · 2015 doi:10.1016/j.gdata.2015.05.039

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
RNA-Seq analysis and whole genome DNA-binding profile of the Vibrio cholerae histone-like nucleoid structuring protein (H-NS).
doi
10.1016/j.gdata.2015.05.039
pmid
26097806
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Julio C Ayala
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Hongxia Wang
[2]
Jorge A Benitez
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Anisia J Silva
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Genomics data
year
2015
abstract
The data described in this article pertain to the genome-wide transcription profiling of a Vibrio cholerae mutant lacking the histone-like nucleoid structuring protein (H-NS) and the mapping of the H-NS chromosome binding sites [1, 2]. H-NS is a nucleoid-associated protein with two interrelated functions: organization of the bacterial nucleoid and transcriptional silencing [3]. Both functions require DNA binding and protein oligomerization [4, 5]. H-NS commonly silences the expression of virulence factors acquired by lateral gene transfer [6]. The highly pleiotropic nature of hns mutants in V. cholerae indicates that H-NS impacts a broad range of cellular processes such as virulence, stress response, surface attachment, biofilm development, motility and chemotaxis. We used a V. cholerae strain harboring a deletion of hns and a strain expressing H-NS tagged at the C-terminus with the FLAG epitope to generate datasets representing the hns transcriptome and DNA binding profile under laboratory conditions (LB medium, 37°C). The datasets are publicly available at the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) with accession numbers GSE62785 and GSE64249.
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Genes exhibiting a fold change ≥±2.0 and q-value < 0.05 were considered differentially expressed in the hns mutant.
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RNA-seq Analysis Identifies New Genes Regulated by the Histone-like Nucleoid Structuring Protein (H-NS) Affecting Vibrio cholerae Virulence, Stress Response and Chemotaxis
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Genome-wide DNA-binding profile of the Vibrio cholerae histone-like nucleoid structuring protein (H-NS)
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H-NS is a nucleoid-associated protein with two interrelated functions: organization of the bacterial nucleoid and transcriptional silencing [3]. Both functions require DNA binding and protein oligomerization [4, 5]. H-NS commonly silences the expression of virulence factors acquired by lateral gene transfer [6]. The highly pleiotropic nature of hns mutants in V. cholerae indicates that H-NS impacts a broad range of cellular processes such as virulence, stress response, surface attachment, biofilm development, motility and chemotaxis. We used a V. cholerae strain harboring a deletion of hns and a strain expressing H-NS tagged at the C-terminus with the FLAG epitope to generate datasets representing the hns transcriptome and DNA binding profile under laboratory conditions (LB medium, 37°C). The datasets are publicly available at the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) with accession numbers GSE62785 and GSE64249.", "claims": [{"id": "claim-method", "statement": "The MACS (Model-Based Analysis for ChIP-Seq) algorithm within SeqMonk was used for peak calling with p-value 1.0E − 05, a sonicated fragment size of 300 bp and input sample as control.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:26097806", "locator": "sections[10] \"ChiP-Seq and data analysis\" paragraph 2", "quote": "The MACS (Model-Based Analysis for ChIP-Seq) algorithm within SeqMonk was used for peak calling with p-value 1.0E − 05, a sonicated fragment size of 300 bp and input sample as control."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The raw and processed RNA-Seq datasets have been deposited in the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) and assigned accession number GSE62785. 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quantitation using the Read Count Quantitation algorithm and annotation of H-NS binding sites.", "Babraham Institute", "http://www.bioinformatics.babraham.ac.uk/projects/seqmonk"]], "row_count": 7, "column_count": 4, "numeric_cells": 4, "header_rows": 1, "locator": "section[8]/table-wrap[1]#t0005"}}, {"id": "asset:table:pmid:26097806:2", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:2ffb29973c20780c118ace708a9c193362ae13c61a1c38dee62f3bbc384dc385", "bytes": 1181, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[8]/table-wrap[2]#t0010", "version": null, "note": "TopHat statistics of the quality control of .fastq files used for alignment.", "structure": {"pmcid": "PMC4470426", "section_index": 8, "section_title": "Differential RNA-Seq and data analysis", "row_count": 11, "column_count": 4}, "table": {"label": "Table 2", "caption": "TopHat statistics of the quality control of .fastq files used for alignment.", "rows": [["Analysis", "Sample (GEO accession #)", "Forward sequencing reads (overall alignment rate)", "Reverse sequencing reads (overall alignment rate)"], ["RNA-Seq OD600 0.5", "Wild type sample 1 (GSM1533384)", "67,772,927 (81.4%)", "67,729,235 (78.7%)"], ["Δhns sample 1 (GSM1533385)", "45,204,039 (81.6%)", "45,181,086 (79.6%)"], ["Wild type sample 2 (GSM1533386)", "39,404,653 (79.7%)", "39,388,107 (78.1%)"], ["Δhns sample 2 (GSM1533387)", "40,998,335 (80.2%)", "40,981,501 (78.4%)"], ["RNA-Seq OD600 2.0", "Wild type sample 1 (GSM1533388)", "35,001,271 (76.6%)", "34,973,987 (75.6%)"], ["Δhns sample 1 (GSM1533389)", "43,629,892 (75.9%)", "43,605,111 (74.9%)"], ["Wild type sample 2 (GSM1533390)", "36,404,561 (72.6%)", "36,375,868 (71.8%)"], ["Δhns sample 2 (GSM1533391)", "38,798,568 (74.4%)", "38,776,510 (73.3%)"], ["ChIP-SeqOD600 0.5", "Anti-FLAG (GSM1567051)", "57,236,395 (63.0%)", "57,236,395 (63.0%)"], ["Input control (GSM1567052)", "58,286,380 (84.2%)", "58,286,380 (84.2%)"]], "row_count": 11, "column_count": 4, "numeric_cells": 33, "header_rows": 1, "locator": "section[8]/table-wrap[2]#t0010"}}], "gaps": ["asset:data:geo:GSE62785 not downloaded", "asset:data:geo:GSE62785 licence not read", "asset:data:geo:GSE64249 not downloaded", "asset:data:geo:GSE64249 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": null, "specific": null, "label": "MACS (Model-Based Analysis for ChIP-Seq)", "dsl_operations": [], "missing_operations": [], "expressible": null, "parameters": {}, "data_shapes": [], "evidence": {"score": 1.0, "band": "verbatim", "quote": "The MACS (Model-Based Analysis for ChIP-Seq) algorithm within SeqMonk was used for peak calling with p-value 1.0E − 05, a sonicated fragment size of 300 bp and input sample as control."}}], "targets": [], "gaps": ["method.reader_named_unmapped"]}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "blocked", "tier": "R4", "blocking_axis": "method", "blocked_on": "method:not_determinable", "axes": {"method": {"tier": "R4", "expressible": false, "required_operations": [], "missing_operations": [], "basis": "The reader quoted the method the paper names (MACS (Model-Based Analysis for ChIP-Seq)), but the corpus's method extractor could not map it onto a DSL operation, so the method is published but not expressible."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. 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