Two paralogues of N-ethylmaleimide sensitive factor: An exception to the minimal vesicular trafficking machinery ofGiardia

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Abstract

Vesicular trafficking plays a critical role in the survival of the human gut pathogen Giardia lamblia as it drives nutrient uptake and morphological stage transition. Unlike most eukaryotes, Giardia has a minimal vesicular trafficking machinery. Herein, we report a rare exception to this minimalism wherein two paralogues of NSF, a crucial factor driving vesicular trafficking by uncoupling the cis-SNARE bundle, are present in this unicellular parasite. While GlNSF 114776 and GlNSF 112681 share very high sequence homology, they are likely to have distinct cellular roles as they exhibit differences in their affinities towards the Glα-SNAPs and display non-overlapping distribution in encysting trophozoites. Under multiple stress conditions (nutritional, oxidative and nitrosative), while GlNSF 112681 remains at peripheral vesicles, GlNSF 114776 relocalizes to the anterior flagella-associated striated fibres, indicating a possible role in regulating flagellar motility. At this location, GlNSF 114776 is likely to perform a 20S complex independent function as neither Glα-SNAPs nor GlSNAREs are present there. The two paralogues are likely needed for stress adaptation as both copies have also been retained in Giardia genomes isolated from clinical samples. This non-canonical function of the GlNSF 114776 may have evolved to support the unique architecture and motility of the anterior flagella.

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