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pubmed:abstractText |
The biosynthesis of the variant surface glycoprotein (VSG) and its release from the surface of Trypanosoma brucei 427 variant clone MITat 1.4 (117) during in vitro transformation of bloodstream trypomastigotes to procyclic trypomastigotes was investigated. After transfer to the transformation medium at 27 degrees C, VSG synthesis is repressed with a half-time, t1/2 = 30 min. Concomitantly VSG-specific mRNA is lost suggesting that repression operates at the transcriptional level. The expression-linked extra gene copy, which codes for VSG, is retained during and after completion of transformation. After repression of VSG synthesis, surface VSG is shed from the cells into the culture medium. During release part of VSG (apparent mol. wt. 61 000) is proteolytically cleaved to a product (apparent mol. wt. 51 000) which represents the N-terminal domain of the protein as judged by the absence of the carbohydrate moiety normally linked to the C terminus.
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