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dc.contributor.authorCapewell, Paul
dc.contributor.authorMonk, Stephanie
dc.contributor.authorIvens, Alasdair
dc.contributor.authorMacgregor, Paula
dc.contributor.authorFenn, Katelyn
dc.contributor.authorWalrad, Pegine
dc.contributor.authorBringaud, Frederic
dc.contributor.authorSmith, Terry K
dc.contributor.authorMatthews, Keith R
dc.date.accessioned2014-07-16T16:01:04Z
dc.date.available2014-07-16T16:01:04Z
dc.date.issued2013-06-26
dc.identifier118164916
dc.identifiere3ea18bb-3216-40b8-8d86-849c6201a347
dc.identifier23840587
dc.identifier000321424400067
dc.identifier84879481263
dc.identifier.citationCapewell , P , Monk , S , Ivens , A , Macgregor , P , Fenn , K , Walrad , P , Bringaud , F , Smith , T K & Matthews , K R 2013 , ' Regulation of Trypanosoma brucei total and polysomal mRNA during development within its mammalian host ' , PLoS One , vol. 8 , no. 6 , e67069 . https://doi.org/10.1371/journal.pone.0067069en
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/10023/5036
dc.descriptionThis work was supported by a Wellcome Trust Programme grant to KM and by a Wellcome Trust Strategic award to the Centre for Immunity, Infection and Evolution at the University of Edinburgh. SM was supported by a studentship from the Medical Research Council, UK.en
dc.description.abstractThe gene expression of Trypanosoma brucei has been examined extensively in the blood of mammalian hosts and in forms found in the midgut of its arthropod vector, the tsetse fly. However, trypanosomes also undergo development within the mammalian bloodstream as they progress from morphologically 'slender forms' to transmissible 'stumpy forms' through morphological intermediates. This transition is temporally progressive within the first wave of parasitaemia such that gene expression can be monitored in relatively pure slender and stumpy populations as well as during the progression between these extremes. The development also represents the progression of cells from translationally active forms adapted for proliferation in the host to translationally quiescent forms, adapted for transmission. We have used metabolic labelling to quantitate translational activity in slender forms, stumpy forms and in forms undergoing early differentiation to procyclic forms in vitro. Thereafter we have examined the cohort of total mRNAs that are enriched throughout development in the mammalian bloodstream (slender, intermediate and stumpy forms), irrespective of strain, revealing those that exhibit consistent developmental regulation rather than sample specific changes. Transcripts that cosediment with polysomes in stumpy forms and slender forms have also been enriched to identify transcripts that escape translational repression prior to transmission. Combined, the expression and polysomal association of transcripts as trypanosomes undergo development in the mammalian bloodstream have been defined, providing a resource for trypanosome researchers. This facilitates the identification of those that undergo developmental regulation in the bloodstream and therefore those likely to have a role in the survival and capacity for transmission of stumpy forms.
dc.format.extent14
dc.format.extent1848843
dc.language.isoeng
dc.relation.ispartofPLoS Oneen
dc.subjectQH426 Geneticsen
dc.subject.lccQH426en
dc.titleRegulation of Trypanosoma brucei total and polysomal mRNA during development within its mammalian hosten
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doi10.1371/journal.pone.0067069
dc.description.statusPeer revieweden


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