Trypanosoma brucei is still the only kinetoplastid known to undergo genetic
exchange, but it seems unreasonable to suppose that it evolved this proces
s all by itself. The position of T. brucei on a molecular phylogenetic tree
constructed from 18S ribosomal RNA gene sequences offers no clues to the l
ikely existence of genetic exchange in trypanosome species other than the S
alivaria, because this group of trypanosomes appears to have diverged from
the rest a very long time ago. Antigenic variation is one characteristic sh
ared by the Salivaria, which has been particularly well-studied in T. bruce
i. The large proportion of the genome devoted to variant antigen genes and
related sequences in T. brucei, suggests a possible role for genetic exchan
ge in enhancing the diversity of the repertoire. Alternatively, genetic exc
hange may counter potential excessive double-strand DNA damage brought abou
t by the DNA rearrangements associated with antigenic variation. The remark
able biparental inheritance of organelle DNA ( = kinetoplast DNA) in T. bru
cei is without precedent in other eukaryotes. The result of genetic exchang
e is to enhance the heterogeneity of the kinetoplast DNA minicircles. (C) 2
001 Australian Society for Parasitology Inc. Published by Elsevier Science
Ltd. All rights reserved.