The expression of the major shed Trypanosoma cruzi antigen results from the developmentally‐regulated transcription of a small gene family
- 25 March 1991
- journal article
- Published by Wiley in FEBS Letters
- Vol. 280 (2) , 316-320
- https://doi.org/10.1016/0014-5793(91)80320-3
Abstract
To better understand the mechanisms involved in the developmental expression of Trypanosoma cruzi antigens we examined the gene structure and transcription properties of the major shed trypomastigote (SAPA). We report in this paper that SAPA is encoded by a small family of at least 6 genes which differ mainly in the length of a repeat region made up of tandemly arranged 36‐bp repeat units. SAPA genes are located distant from chromosomal telomeres as inferred from their insensitivity to Ba131 nuclease treatment. Furthermore, Northern blot and S1 protection analyses strongly support the fact that most (or all) SAPA genes are transcribed in the infective form of the parasite.Keywords
This publication has 10 references indexed in Scilit:
- Fetal IgG specificities against Trypanosoma cruzi antigens in infected newborns.Proceedings of the National Academy of Sciences, 1990
- The 85-kd surface antigen gene of Trypanosoma cruzi is telomeric and a member of a multigene family.The EMBO Journal, 1989
- Trypanosoma cruzi expresses diverse repetitive protein antigensInfection and Immunity, 1989
- Identification of a Trypanosoma cruzi antigen that is shed during the acute phase of Chagas' diseaseMolecular and Biochemical Parasitology, 1989
- Multiple Trypanosoma cruzi antigens containing tandemly repeated amino acid sequence motifsMolecular and Biochemical Parasitology, 1988
- Antigenic determinants of Trypanosoma cruzi defined by cloning of parasite DNAMolecular and Biochemical Parasitology, 1987
- Trypanosoma cruzi: Structure and Transcription of Kinetoplast DNA Maxicircles of Cloned Stocks12The Journal of Protozoology, 1986
- Temporal variations in dissolved selenium in a coastal ecosystemNature, 1982
- Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybridsCell, 1977