Show simple item record

dc.contributor.authorElias, Dwayne A.
dc.contributor.authorMukhopadhyay, A.
dc.contributor.authorJoachimiak, M. P.
dc.contributor.authorDrury, Elliott C.
dc.contributor.authorRedding, Alyssa M.
dc.contributor.authorYen, Huei-Che B.
dc.contributor.authorFields, Matthew W.
dc.contributor.authorHazen, Terry C.
dc.contributor.authorArkin, Adam P.
dc.contributor.authorKeasling, J. D.
dc.contributor.authorWall, Judy D.
dc.date.accessioned2017-07-12T19:12:45Z
dc.date.available2017-07-12T19:12:45Z
dc.date.issued2009-03
dc.identifier.citationElias DA, Drury EC, Redding AM, Mukhopadyay A, Yen HC, Fields MW, Hazen TC, Arkin AP, Keasling JD, Wall JD, "Expression profiling of hypothetical genes in Desulfovibrio vulgaris leads to improved functional annotation," Nucleic Acids Res 2009 37(9):2926–2939en_US
dc.identifier.issn0305-1048
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/13224
dc.description.abstractHypothetical (HyP) and conserved HyP genes account for >30% of sequenced bacterial genomes. For the sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough, 347 of the 3634 genes were annotated as conserved HyP (9.5%) along with 887 HyP genes (24.4%). Given the large fraction of the genome, it is plausible that some of these genes serve critical cellular roles. The study goals were to determine which genes were expressed and provide a more functionally based annotation. To accomplish this, expression profiles of 1234 HyP and conserved genes were used from transcriptomic datasets of 11 environmental stresses, complemented with shotgun LC–MS/MS and AMT tag proteomic data. Genes were divided into putatively polycistronic operons and those predicted to be monocistronic, then classified by basal expression levels and grouped according to changes in expression for one or multiple stresses. One thousand two hundred and twelve of these genes were transcribed with 786 producing detectable proteins. There was no evidence for expression of 17 predicted genes. Except for the latter, monocistronic gene annotation was expanded using the above criteria along with matching Clusters of Orthologous Groups. Polycistronic genes were annotated in the same manner with inferences from their proximity to more confidently annotated genes. Two targeted deletion mutants were used as test cases to determine the relevance of the inferred functional annotations.en_US
dc.titleExpression profiling of hypothetical genes in Desulfovibrio vulgaris leads to improved functional annotationen_US
dc.typeArticleen_US
mus.citation.extentfirstpage2926en_US
mus.citation.extentlastpage2939en_US
mus.citation.issue9en_US
mus.citation.journaltitleNucleic Acids Researchen_US
mus.citation.volume37en_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.doi10.1093/nar/gkp164en_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemical Engineering.en_US
mus.relation.departmentMicrobiology & Immunology.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.data.thumbpage7en_US
mus.contributor.orcidFields, Matthew W.|0000-0001-9053-1849en_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record


MSU uses DSpace software, copyright © 2002-2017  Duraspace. For library collections that are not accessible, we are committed to providing reasonable accommodations and timely access to users with disabilities. For assistance, please submit an accessibility request for library material.