Trypanosoma brucei is a protozoan flagellate that causes African sleeping sickness.Flagellar function in this organism is critical for life cycle progression and pathogenesis,however the regulation of flagellar motili...Trypanosoma brucei is a protozoan flagellate that causes African sleeping sickness.Flagellar function in this organism is critical for life cycle progression and pathogenesis,however the regulation of flagellar motility is not well understood.The flagellar axoneme produces a complex beat through the pre-cisely coordinated firing of many proteins,including multiple dynein motors.These motors are found in the inner arm and outer arm complexes.We are studying one of the inner arm dynein motors in the T.brucei flagellum:dynein-f.RNAi knockdown of genes for two components of dynein-f:DNAH10,theαheavy chain,and IC138,an intermediate chain,cause severe motility defects including immotility.To determine if motility defects result from structural disruption of the axoneme,we used two different flagellar preparations to carefully examine axoneme structure in these strains using transmission electron microscopy(TEM).Our analysis showed that inner arm dynein size,axoneme structural integrity and fixed central pair orientation are not significantly different in either knockdown culture when compared to control cultures.These results support the idea that immotility in knockdowns affecting DNAH10 or IC138 results from loss of dynein-f function rather than from obvious structural defects in the axoneme.展开更多
文摘Trypanosoma brucei is a protozoan flagellate that causes African sleeping sickness.Flagellar function in this organism is critical for life cycle progression and pathogenesis,however the regulation of flagellar motility is not well understood.The flagellar axoneme produces a complex beat through the pre-cisely coordinated firing of many proteins,including multiple dynein motors.These motors are found in the inner arm and outer arm complexes.We are studying one of the inner arm dynein motors in the T.brucei flagellum:dynein-f.RNAi knockdown of genes for two components of dynein-f:DNAH10,theαheavy chain,and IC138,an intermediate chain,cause severe motility defects including immotility.To determine if motility defects result from structural disruption of the axoneme,we used two different flagellar preparations to carefully examine axoneme structure in these strains using transmission electron microscopy(TEM).Our analysis showed that inner arm dynein size,axoneme structural integrity and fixed central pair orientation are not significantly different in either knockdown culture when compared to control cultures.These results support the idea that immotility in knockdowns affecting DNAH10 or IC138 results from loss of dynein-f function rather than from obvious structural defects in the axoneme.
