EARLY EXPRESSION OF A TRYPANOSOMA-BRUCEI VSG GENE DUPLICATED FROM AN INCOMPLETE BASIC COPY

Intrachromosomal variant surface glycoprotein (VSG) genes in Trypanoso ma brucei are expressed by a mechanism involving gene conversion. The 3' boundary of gene conversion is usually within the last 130 bp of th e VSG gene, a region of partially conserved sequences. We report here the loss of the predominant telomeric A VSG gene in the cloned variant antigenic type (VAT) 5(A3), leaving only an intrachromosomal A VSG ge ne (the A-B gene). The nucleotide sequence of the A-B VSG gene reveals that it lacks the normal VSG 3' sequence. Surprisingly, we find cells expressing this A-B VSG gene in relapse populations arising from VAT 5(A3) Since the A VSG mRNAs from these cells have a normal 3' sequence , the incomplete A-B VSG gene must be expressed via a partial gene con version that supplies the functional 3' end. Although the A-B VSG gene is no longer predominant like the telomeric A VSG gene, it is still e xpressed more frequently than other intrachromosomal VSG genes, sugges ting that factors other than a telomeric location determine whether a VSG gene is expressed early in a serodeme.