Molecular and Biochemical Parasitology 94 (1998) 249 – 264
Conserved organization of genes in trypanosomatids
1
Fre ´de ´ric Bringaud
a,
*, Ce ´cile Vedrenne
a
, Armelle Cuvillier
a
, Daniel Parzy
b
,
Dominique Baltz
a
, Emmanuel Tetaud
a
, Etienne Pays
c
, Juan Venegas
a,2
,
Gilles Merlin
a
, The ´o Baltz
a
a
Laboratoire de Parasitologie Mole ´culaire, Uniersite ´ Victor Se ´gole `ne de Bordeaux II, UPRESA-5016 CNRS, 146 rue Le ´o Saignat,
33076 Bordeaux cedex, France
b
Laboratoire de Parasitologie, IMTSSA, Bd Charles Liom, Parc du Pharo, 13007 Marseille, France
c
De ´partement de Biologie Mole ´culaire, Uniersite ´ libre de Bruxelles, 67 rue des cheaux, B1640 Rhode St Gene `se, Belgium
Received 2 March 1998; received in revised form 29 May 1998; accepted 2 June 1998
Abstract
Trypanosomatids are unicellular protozoan parasites which constitute some of the most primitive eukaryotes.
Leishmania spp, Trypanosoma cruzi and members of the Trypanosoma brucei group, which cause human diseases, are
the most studied representatives of this large family. Here we report a comparative analysis of a large genomic region
containing glucose transporter genes in three Salivarian trypanosomes (T. brucei, T. congolense and T. iax ), T. cruzi
and Leishmania donoani. In T. brucei, the 8 kb (upstream) and 14 kb (downstream) regions flanking the glucose
transporter genes cluster contain two and six new genes, respectively, six of them encoding proteins homologous to
known eukaryotic proteins (phosphatidylinositol 3 kinase, ribosomal protein S12, DNAJ and three small G-
proteins — Rab1, YPT6 and ARL3). This gene organization is identical in T. brucei, T. congolense and T. iax
suggesting that Salivarian trypanosomes have a high level of conservation in gene organization. In T. cruzi and
Leishmania, the overall organization of this cluster is conserved, with insertion of additional genes when compared
with T. brucei. Phylogenetic reconstitution based on glucose transporters is in accord with the monophyly of the
Abbreiations: ARL3, ADP ribosylation factor like 3; ORF, open reading frame; PI3K, phosphatidylinositol 3 kinase; RPS12,
ribosomal protein S12; THT, trypanosome hexose transporter from T. brucei ; TcoHT, from T. congolense ; TcrHT, from T. cruzi ;
TvHT, from T. iax.
* Corresponding author. Fax: +33 5 57571015; e-mail: bringaud@u-bordeaux2.fr
1
Note: The GenBank accession numbers are: AF031925 (T. brucei :5 THT-flanking region), AF031926 and AF032098 (T. brucei :
3 THT-flanking region), AF031927 (CosTcr1 clone of T. cruzi :3 TcrHT-flanking region), AF031928 (CosTcr2 clone of T. cruzi :
ORF1 downstream of the retrotransposon), AF032096 (T. congolense : unit repeat containing the TcoHT1 gene) and AF032097 (T.
congolense : unit repeat containing the TcoHT2 gene).
2
Present address: Instituto de Ciencias Biome ´dicas (ICBM), Facultad de Medicina, Independencia 1027, Casilla 70086-Stgo-7,
Chile.
0166-6851/98/$19.00 © 1998 Elsevier Science B.V. All rights reserved.
PII S0166-6851(98)00080-2