کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5915777 | 1163328 | 2010 | 4 صفحه PDF | دانلود رایگان |
TbKif13-2, a member of the microtubule-depolymerising Kinesin-13 family was localised at the tip of the flagellum in Trypanosoma brucei. Its predicted activity suggested a role in the regulation of axonemal length. However, using gene deletion and overexpression of TbKif13-2 we show that, in procyclic T. brucei, this kinesin has only a very limited effect on flagellar length. Gene deletion resulted in no significant elongation of the flagellum and overexpression only slightly decreased flagellar length and the rate of growth of a new flagellum during cell division. This is in contrast to studies in Leishmania major, where overexpression of the TbKif13-2 homologue resulted in a significant length reduction of the flagellum. Knockout of TbKif13-2 has, however, an effect on the initial growth of the emerging new flagellum. In conclusion, we show that TbKif13-2 has only a marginal impact on flagellar length in T. brucei.
Trypanosoma brucei contains at least five microtubule-depolymerising kinesins, but the flagellar kinesin TbKif13-2 has only a moderate effect on flagellar dynamics.84Research highlightsⶠThe depolymerising kinesin TbKif13-2 is localised at the tip of the mature and new flagellum of T. brucei. ⶠA gene deletion mutant of this kinesin has no measurable effect on the length of the flagellum. ⶠOverexpression of a myc-tagged TbKif13-2 has marginal, but significant effects on the initial rate of outgrowth of the new flagellum and on the length of the mature flagellum.
Journal: Molecular and Biochemical Parasitology - Volume 174, Issue 2, December 2010, Pages 137-140