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dc.contributor.authorWong, Sandy M. S.
dc.contributor.authorAkerley, Brian J.
dc.date2022-08-11T08:09:25.000
dc.date.accessioned2022-08-23T16:29:54Z
dc.date.available2022-08-23T16:29:54Z
dc.date.issued2003-10-18
dc.date.submitted2010-02-01
dc.identifier.citationGene. 2003 Oct 16;316:177-86.
dc.identifier.issn0378-1119 (Print)
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37353
dc.description.abstractComplete bacterial genomic DNA sequences have allowed application of genome-scale strategies to identify essential genes. Efficient generation of conditional loss of function mutations provides a means of characterization of this class of genes. Promoter systems conferring tight regulation are particularly applicable to generating such mutations and we sought to apply this approach for the analysis of an essential gene of Haemophilus influenzae. Therefore, we developed the use of a D-xylose-inducible promoter for verification of an essential role in growth for yraM, which encodes a putative periplasmic lipoprotein, in both H. influenzae Rd and virulent type b strains. This promoter was sufficiently tightly regulated to generate conditionally viable strains by inducible expression of YraM. A second approach was used to further characterize YraM. Natural transformation and an ordered mutant collection spanning the H. influenzae genome provide the means to target any gene of interest for mutagenesis and temperature-sensitive (TS) mutant isolation. This strategy was applied to generate a conditionally lethal allele of yraM. The resulting TS mutation was directly mapped to a single amino acid substitution within a motif conserved in all putative YraM orthologs and this mutation was shown to be sufficient to confer the TS phenotype.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=14563564&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/S0378-1119(03)00762-5
dc.subjectBacterial Proteins
dc.subjectCell Division
dc.subjectDNA Transposable Elements
dc.subjectGene Deletion
dc.subjectGene Expression Regulation, Bacterial
dc.subjectGenetic Complementation Test
dc.subjectGenetic Markers
dc.subjectGenomics
dc.subjectHaemophilus influenzae
dc.subjectMutagenesis, Insertional
dc.subjectMutagenesis, Site-Directed
dc.subjectMutation
dc.subjectPromoter Regions, Genetic
dc.subjectTemperature
dc.subjectTime Factors
dc.subjectXylose
dc.subjectMicrobiology
dc.subjectMolecular Genetics
dc.titleInducible expression system and marker-linked mutagenesis approach for functional genomics of Haemophilus influenzae
dc.typeJournal Article
dc.source.journaltitleGene
dc.source.volume316
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/mgm_pp/18
dc.identifier.contextkey1127077
html.description.abstract<p>Complete bacterial genomic DNA sequences have allowed application of genome-scale strategies to identify essential genes. Efficient generation of conditional loss of function mutations provides a means of characterization of this class of genes. Promoter systems conferring tight regulation are particularly applicable to generating such mutations and we sought to apply this approach for the analysis of an essential gene of Haemophilus influenzae. Therefore, we developed the use of a D-xylose-inducible promoter for verification of an essential role in growth for yraM, which encodes a putative periplasmic lipoprotein, in both H. influenzae Rd and virulent type b strains. This promoter was sufficiently tightly regulated to generate conditionally viable strains by inducible expression of YraM. A second approach was used to further characterize YraM. Natural transformation and an ordered mutant collection spanning the H. influenzae genome provide the means to target any gene of interest for mutagenesis and temperature-sensitive (TS) mutant isolation. This strategy was applied to generate a conditionally lethal allele of yraM. The resulting TS mutation was directly mapped to a single amino acid substitution within a motif conserved in all putative YraM orthologs and this mutation was shown to be sufficient to confer the TS phenotype.</p>
dc.identifier.submissionpathmgm_pp/18
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.source.pages177-86


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