CONSERVATION OF MITOCHONDRIAL TARGETING SEQUENCE FUNCTION IN MITOCHONDRIAL AND HYDROGENOSOMAL PROTEINS FROM THE EARLY-BRANCHING EUKARYOTES CRITHIDIA, TRYPANOSOMA AND TRICHOMONAS
T. Hausler et al., CONSERVATION OF MITOCHONDRIAL TARGETING SEQUENCE FUNCTION IN MITOCHONDRIAL AND HYDROGENOSOMAL PROTEINS FROM THE EARLY-BRANCHING EUKARYOTES CRITHIDIA, TRYPANOSOMA AND TRICHOMONAS, European journal of cell biology, 73(3), 1997, pp. 240-251
Kinetoplastid protozoa are the earliest-branching eukaryotes to posses
s a true mitochondrion. This organelle is host to a variety of intrigu
ing and unique features, including RNA editing. We examined the charac
teristics of protein import into mitochondria of Trypanosoma brucei. D
ihydrofolate reductase (DHFR) carrying a yeast mitochondrial targeting
signal was correctly translocated into trypanosome mitochondria in vi
vo, as were DHFR fusion proteins bearing two unusually short (7-9 amin
o acids) presequences from trypanosomatids. The short trypanosomal tar
geting signals were functional in Saccharomyces cerevisiae as well, bu
t their targeting efficiency was lower and processing was absent. Tric
homonads branched even earlier than kinetoplastids in eukaryotic evolu
tion and contain energy-generating organelles called hydro genosomes.
The origin of hydrogenosomes has been controversial, but most evidence
suggests that they are related to mitochondria. Putative hydrogenosom
al targeting signals from Trichomonas vaginalis are short (5-12 amino
acids). Three such sequences were capable of targeting a passenger pro
tein to mitochondria both in yeast and in trypanosomes, and one of the
hydrogenosomal presequences was effi ciently processed in both organi
sms. These findings suggest a resemblance between the import machineri
es of mitochondria and hydrogenosomes.