Show simple item record

dc.contributor.authorDavies, Bryan W.
dc.contributor.authorGhosal, Anubrata
dc.contributor.authorKoehrer, Caroline
dc.contributor.authorBabu, Vignesh M.P.
dc.contributor.authorYamanaka, Kinrin
dc.contributor.authorJacob, Asha I
dc.contributor.authorFerullo, Daniel J.
dc.contributor.authorGruber, Charley C
dc.contributor.authorVercruysse, Maarten
dc.contributor.authorWalker, Graham C.
dc.date.accessioned2018-07-12T19:39:06Z
dc.date.available2018-07-12T19:39:06Z
dc.date.issued2017-01
dc.date.submitted2017-01
dc.identifier.issn0006-291X
dc.identifier.issn1090-2104
dc.identifier.urihttp://hdl.handle.net/1721.1/116955
dc.description.abstractThe product of the human C21orf57 (huYBEY) gene is predicted to be a homologue of the highly conserved YbeY proteins found in nearly all bacteria. We show that, like its bacterial and chloroplast counterparts, the HuYbeY protein is an RNase and that it retains sufficient function in common with bacterial YbeY proteins to partially suppress numerous aspects of the complex phenotype of an Escherichia coli ΔybeY mutant. Expression of HuYbeY in Saccharomyces cerevisiae, which lacks a YbeY homologue, results in a severe growth phenotype. This observation suggests that the function of HuYbeY in human cells is likely regulated through specific interactions with partner proteins similarly to the way YbeY is regulated in bacteria.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM31010)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM17151)en_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.BBRC.2017.01.149en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleC21orf57 is a human homologue of bacterial YbeY proteinsen_US
dc.typeArticleen_US
dc.identifier.citationGhosal, Anubrata et al. “C21orf57 Is a Human Homologue of Bacterial YbeY Proteins.” Biochemical and Biophysical Research Communications 484, 3 (March 2017): 612–617 © 2017 Elsevier Incen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorGhosal, Anubrata
dc.contributor.mitauthorKoehrer, Caroline
dc.contributor.mitauthorBabu, Vignesh M.P.
dc.contributor.mitauthorYamanaka, Kinrin
dc.contributor.mitauthorJacob, Asha I
dc.contributor.mitauthorFerullo, Daniel J.
dc.contributor.mitauthorGruber, Charley C
dc.contributor.mitauthorVercruysse, Maarten
dc.contributor.mitauthorWalker, Graham C
dc.relation.journalBiochemical and Biophysical Research Communicationsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-07-12T13:34:29Z
dspace.orderedauthorsGhosal, Anubrata; Köhrer, Caroline; Babu, Vignesh M.P.; Yamanaka, Kinrin; Davies, Bryan W.; Jacob, Asha I.; Ferullo, Daniel J.; Gruber, Charley C.; Vercruysse, Maarten; Walker, Graham C.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8465-3433
dc.identifier.orcidhttps://orcid.org/0000-0001-5539-4391
dc.identifier.orcidhttps://orcid.org/0000-0003-1777-1082
dc.identifier.orcidhttps://orcid.org/0000-0002-7127-9833
dc.identifier.orcidhttps://orcid.org/0000-0001-7243-8261
mit.licensePUBLISHER_CCen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record