More surprises from Kinetoplastida
Open Access
- 16 March 1999
- journal article
- editorial
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 96 (6) , 2579-2581
- https://doi.org/10.1073/pnas.96.6.2579
Abstract
Protozoan parasites of the order Kinetoplastida include various species of the genera Leishmania and Trypanosoma that are responsible for substantial human morbidity and mortality in the tropics. Pathogenic Leishmania species cause a diverse group of diseases, collectively called leishmaniasis, that range in severity from spontaneously healing skin ulcers to fatal visceral disease. African and American trypanosomes cause fatal sleeping sickness and debilitating Chagas disease, respectively. More than a billion people live in areas inhabited by the insects that transmit these parasites, and millions of people are newly infected each year. Organisms of the order Kinetoplastida have a unique organelle called the kinetoplast, an appendix of their single mitochondrion located near the basal body of the flagellum that contains a network of thousands of small interlocking circular DNAs. Kinetoplastids are among the most ancient eukaryotes, with rRNA lineages extending farther back than those of animals, plants, and even fungi (1, 2). As might be expected of such ancient organisms, the kinetoplast is only one of their many distinctive features. The top 10 list of fundamentally important biological phenomena first discovered in Leishmania and trypanosomes includes “programmed” antigenic variation of surface glycoproteins (3), glycosylphosphatidylinositol anchors of membrane proteins (4, 5), expansion/contraction of telomeric DNA repeats (6), bent DNA helices (7), eukaryotic polycistronic transcription (8), trans-splicing of precursor RNAs (9, 10), mitochondrial RNA editing (11), other unique organelles such as glycosomes (12), and distinctive metabolic pathways (13). Several of these phenomena, first unearthed because of their prominence in kinetoplastids, have subsequently been found in higher eukaryotes and have become the focus of intense research interest in those systems. In addition, the many nefarious mechanisms used by Leishmania and trypanosomes to thwart immune defenses thrown at them by their mammalian hosts have led to an enhanced appreciation of the diversity and …This publication has 30 references indexed in Scilit:
- Localization of nine glycolytic enzymes in a microbody‐like organelle in Trypanosoma brucei: The glycosomePublished by Wiley ,2001
- Chromosome 2 Sequence of the Human Malaria ParasitePlasmodium falciparumScience, 1998
- Conserved organization of genes in trypanosomatidsMolecular and Biochemical Parasitology, 1998
- The Saccharomyces cerevisiae kinetochoreFEBS Letters, 1996
- Structure and Function of Kinetochores in Budding YeastAnnual Review of Cell and Developmental Biology, 1995
- A common pyrimidine-rich motif governs trans-splicing and polyadenylation of tubulin polycistronic pre-mRNA in trypanosomes.Genes & Development, 1994
- The 35-Nucleotide Spliced Leader Sequence Is Common to All Trypanosome Messenger RNA'sScience, 1986
- Growth of chromosome ends in multiplying trypanosomesNature, 1983
- Transcripts coding for variant surface glycoproteins of Trypanosoma brucei have a short, identical exon at their 5′ endGene, 1982
- N-terminal amino acid sequences of variant-specific surface antigens from Trypanosoma bruceiNature, 1976