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dc.contributor.authorMosonik, N.C
dc.contributor.authorMurphy, N.B
dc.contributor.authorPelle, R
dc.contributor.authorKinyanjui, P.W
dc.date.accessioned2013-03-21T09:48:52Z
dc.date.issued2004
dc.identifier.citationInternational Journal of BioChemiPhysics, Vol. 13, No.2, December 2004en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/14884
dc.description.abstractTrypanosoma congolense parasites are routinely propagated in vitro in many laboratories for various studies. However it is important to know whether the in vitro propagated parasites express the same genes as the in vivo generated parasites. To address this question procyclic trypanosomes of T. congolense ILl180 were isolated from both infected tsetse flies and culture. Total mRNA was prepared from the two types of trypanosomes. The mRNA was used as template to synthesize cDNAs. The cDNAs were subsequently used in randomly amplified differentially expressed sequences (RADES) analysis using olgonucleotide primers of arbitrary sequence. The primers revealed differences in cDNA products generated by the mRNAs from in vitro and in vivo parasites suggesting differences in the genes expressed by the two forms oftrypanosomes. Primer 899 amplified a 280 bp in vivo specific product. The product was cloned and used to probe genomic DNA from T. congolense IL1l80. The product identified a gene that is either single copy with two alleles or a gene that has two alleles and a few tandem repeats. The 280bp DNA fragment was sequenced and analysis of the sequence revealed a gene product with significant homology in one domain to eukaryotic Ll9 ribosomal gene product.en
dc.language.isoenen
dc.titleDifferential expression of a DNA fragment obtained from in vivo and in vitro propagated parasites of Trypanosoma congolenseen
dc.typeArticleen
local.embargo.terms6 monthsen
local.publisherInternational Livestock Research Instituteen
local.publisherDepartment of Biochemistry, University of Nairobien


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