Molecular cloning, characterization and overexpression of a novel cyclin from Leishmania mexicana.

dc.FacultyEndemic Diseasesen_US
dc.contributor.authorIbrahim, Muntaser E.
dc.contributor.authorGrant, KM
dc.contributor.authorMottram, JC
dc.contributor.editoren_US
dc.contributor.otherClinical Pathology and Immunologyen_US
dc.date2013
dc.date.accessioned2015-11-23T07:35:23Z
dc.date.available2015-11-23T07:35:23Z
dc.date.issued2015-11-23
dc.date.submitted2015-11-23
dc.description.abstractWe are reporting here, the cloning and characterization of the first cyclin from Leishmania mexicana. We have identified a cyclin-like motif from the L. major genome sequencing project. A cyclin homologue was cloned and sequenced from L. mexicana genome and it showed 96.1% amino acid identity with the putative L. major cyclin. It has also sequence identity to mitotic cyclins from other organisms. Southern analysis showed that it is present as a single copy gene. CYCa has been over-expressed in E. coli as a histidine fusion and western blot has confirmed the immunoreactive property of the recombinant cyclin, which then used to reconstitute active recombinant L. mexicana CRK3. No phosphorylation of histone HI was detected by both wild type and mutated CRK3 on the activation assays suggesting that phosphorylation status and cyclin binding are important for reconstituting protein kinase activity. The results confirm that we have isolated a cyclin molecule from L. mexicana (LmCYCa) which may play an important role in the regulation of the parasite cell cycle.en_US
dc.identifier.urihttp://khartoumspace.uofk.edu/123456789/17264
dc.publisherUOFKen_US
dc.subjectCloning, Molecularen_US
dc.subjectCyclinsen_US
dc.subjectEscherichia colien_US
dc.subjectLeishmania mexicanaen_US
dc.subjectMolecular Sequence Dataen_US
dc.subjectPhylogenyen_US
dc.subjectProtozoan Proteinsen_US
dc.subjectAmino Acid Sequenceen_US
dc.titleMolecular cloning, characterization and overexpression of a novel cyclin from Leishmania mexicana.en_US
dc.typeArticleen_US

Files