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pmid:26484177

Transcriptional profiling of UlaR-regulated genes in Streptococcus pneumoniae.

Sulman Shafeeq · Muhammad Afzal · Birgitta Henriques-Normark · Oscar P Kuipers

Genomics data · 2015 doi:10.1016/j.gdata.2015.02.004

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Transcriptional profiling of UlaR-regulated genes in Streptococcus pneumoniae.
doi
10.1016/j.gdata.2015.02.004
pmid
26484177
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Sulman Shafeeq
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Muhammad Afzal
[2]
Birgitta Henriques-Normark
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Oscar P Kuipers
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Genomics data
year
2015
abstract
The transcriptional regulator UlaR belongs to the family of PRD-containing transcriptional regulators, which are mostly involved in the regulation of carbohydrate metabolism. The role of the transcriptional regulator UlaR in Streptococcus pneumoniae has recently been described [1]. Here, we report detailed genome-wide transcriptional profiling of UlaR-regulated genes in S. pneumoniae D39 and its ∆ulaR derivative, either in the presence of 10 mM ascorbic acid in M17 medium using microarray analysis. 10 mM concentration of ascorbic acid was supplemented to the M17 medium because our lacZ-fusion studies indicated that UlaR acts as a transcriptional activator of its targets in the presence of ascorbic acid and the expression of the ula operon was maximal at a 10 mM ascorbic acid concentration [1]. All transcriptional profiling data of UlaR-regulated genes was deposited to Gene Expression Omnibus (GEO) database under accession number GSE61649.
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Impact of ulaR delation on the transcriptome of Streptococcus pneumoniae D39 in the presence of ascorbic acid
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Summary of transcriptome comparison of S. pneumoniae strain D39 ΔulaR and D39 wild-type grown in AM17 (10 mM Ascorbic acid + M17).
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The role of the transcriptional regulator UlaR in Streptococcus pneumoniae has recently been described [1]. Here, we report detailed genome-wide transcriptional profiling of UlaR-regulated genes in S. pneumoniae D39 and its ∆ulaR derivative, either in the presence of 10 mM ascorbic acid in M17 medium using microarray analysis. 10 mM concentration of ascorbic acid was supplemented to the M17 medium because our lacZ-fusion studies indicated that UlaR acts as a transcriptional activator of its targets in the presence of ascorbic acid and the expression of the ula operon was maximal at a 10 mM ascorbic acid concentration [1]. 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Hermans"], ["ΔulaR", "D39 ΔulaR; SpecR", "[1]"]], "row_count": 3, "column_count": 3, "numeric_cells": 4, "header_rows": 1, "locator": "section[4]/table-wrap[1]#t0005"}}, {"id": "asset:table:pmid:26484177:2", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:2a10e5609b3ee99e5a9449b2c4725cefa81ccedfbee737c1d379d0e05c2207cf", "bytes": 1959, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[9]/table-wrap[1]#t0010", "version": null, "note": "Summary of transcriptome comparison of S. pneumoniae strain D39 ΔulaR and D39 wild-type grown in AM17 (10 mM Ascorbic acid + M17).", "structure": {"pmcid": "PMC4535465", "section_index": 9, "section_title": "Discussion", "row_count": 22, "column_count": 4}, "table": {"label": "Table 2", "caption": "Summary of transcriptome comparison of S. pneumoniae strain D39 ΔulaR and D39 wild-type grown in AM17 (10 mM Ascorbic acid + M17).", "rows": [["D39 taga", "Functionb", "Ratioc", "p-Values"], ["spd_0063", "Beta-N-acetylhexosaminidase, StrH", "− 2.3", "6.58E-07"], ["spd-0450", "Type I restriction-modification system, S subunit, putative", "− 4.0", "4.98E-08"], ["spd-0452", "Integrase/recombinase, phage integrase family protein", "3.7", "3.40E-11"], ["spd-0608", "Orotidine 5′-phosphate decarboxylase, PyrF", "2.1", "1.50E-03"], ["spd-1046", "6-phospho-beta-galactosidase, LacG", "2.4", "1.39E-08"], ["spd-1047", "PTS system, lactose-specific IIBC components, LacE", "2.4", "2.12E-07"], ["spd-1107", "Guanosine monophosphate reductase, GuaC", "2.4", "1.19E-07"], ["spd-1131", "Carbamoyl-phosphate synthase, large subunit, CarB", "2.3", "1.62E-07"], ["spd-1302", "Oxidoreductase, putative", "− 2.0", "2.03E-03"], ["spd-1324", "IS630-Spn1, transposase Orf2", "2.4", "9.43E-03"], ["spd-1413", "ATP-dependent RNA helicase, putative", "2.3", "4.52E-07"], ["spd_1839", "Transketolase, Tkt", "− 2.3", "9.58E-09"], ["spd_1840", "l-ascorbate 6-phosphate lactonase, UlaG", "− 26.1", "4.16E-09"], ["spd_1841", "BglG family transcriptional regulator, UlaR", "− 7.0", "4.42E-08"], ["spd_1842", "l-ribulose-5-phosphate 4-epimerase, UlaF/AraD", "− 10.1", "1.81E-07"], ["spd_1843", "l-xylulose 5-phosphate 3-epimerase, UlaE", "− 19.1", "1.07E-12"], ["spd_1844", "3-keto-l-gulonate-6-phosphate decarboxylase, UlaD", "− 25.8", "4.50E-13"], ["spd_1845", "Ascorbate-specific PTS system, IIA component, UlaC", "− 12.4", "8.74E-09"], ["spd_1846", "Ascorbate-specific PTS system, IIB component, UlaB", "− 24.7", "7.72E-10"], ["spd_1847", "Ascorbate-specific PTS system, IIC component, UlaA", "− 9.5", "1.75E-08"], ["spd_1913", "Phosphate ABC transporter, ATP-binding protein, PstB", "2.1", "2.30E-04"]], "row_count": 22, "column_count": 4, "numeric_cells": 71, "header_rows": 1, "locator": "section[9]/table-wrap[1]#t0010"}}], "gaps": ["asset:data:geo:GSE61649 not downloaded", "asset:data:geo:GSE61649 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": null, "specific": null, "label": "CyberT implementation of a variant of t-test", "dsl_operations": [], "missing_operations": [], "expressible": null, "parameters": {}, "data_shapes": [], "evidence": {"score": 1.0, "band": "verbatim", "quote": "CyberT implementation of a variant of t-test (http://bioinformatics.biol.rug.nl/cybert/index.shtml) was performed and false discovery rates (FDRs) were calculated as described [7]."}}], "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 (CyberT implementation of a variant of t-test), 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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