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Abstract:

Gene expression in trypanosomes is controlled mainly by post-transcriptional processes. This study was designed to analyse HX1, one of the TcP2β upstream intergenic regions. It is an efficient pre-mRNA processing region that has been widely and successfully used in Trypanosoma cruzi transfection vectors. Herein we compared its performance with other regions within the same locus, and we identified the sequence elements responsible for the HX1 efficiency in trans-splicing and protein synthesis. Our mutational analysis showed the flexibility of the branch point site selection for HX1 trans-splicing process. We demonstrated also that its 12 nt 5′UTR sequence contributes to both trans-splicing and translation efficiency. The natural insertion of the repetitive element short interspersed repetitive element (SIRE) in one of the HX1 polypyrimidine tracts decreases the translated protein level by 40%. In this report, we demonstrated that this reduction is a consequence of a decrease of five-fold in the level of processed mRNA balanced by an increased efficiency of translation due to the inclusion of a 38 nt SIRE specific sequence in the 5′UTR of the mRNA. © 2005 Elsevier B.V. All rights reserved.

Registro:

Documento: Artículo
Título:Analysis of the highly efficient pre-mRNA processing region HX1 of Trypanosoma cruzi
Autor:Ben-Dov, C.P.; Levin, M.J.; Vázquez, M.P.
Filiación:Lab. Biol. Molec. Enfermedad Chagas, INGEBI-CONICET, University of Buenos Aires, Vuelta de Obligado 2490 2P, 1428 Buenos Aires, Argentina
Programme of Gene Regulation, Centre for Genomic Regulation, 08003 Barcelona, Spain
Palabras clave:Chagas disease; Post-transcriptional regulation; Repetitive sequences; trans-Splicing; messenger RNA; ribosome protein; 5' untranslated region; article; gene locus; mutational analysis; nonhuman; priority journal; protein analysis; protein synthesis; RNA processing; trans splicing; transcription regulation; Trypanosoma cruzi; insertion sequences; Trypanosoma; Trypanosoma cruzi; Trypanosoma cruzi
Año:2005
Volumen:140
Número:1
Página de inicio:97
Página de fin:105
DOI: http://dx.doi.org/10.1016/j.molbiopara.2005.01.001
Título revista:Molecular and Biochemical Parasitology
Título revista abreviado:Mol. Biochem. Parasitol.
ISSN:01666851
CODEN:MBIPD
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01666851_v140_n1_p97_BenDov

Referencias:

  • Vanhamme, L., Pays, E., Control of gene expression in trypanosomes (1995) Microbiol Rev, 59, pp. 223-240
  • Liang, X.H., Haritan, A., Uliel, S., Michaeli, S., Trans and cis splicing in trypanosomatids: Mechanism, factors, and regulation (2003) Eukaryot Cell, 2, pp. 830-840
  • Clayton, C.E., Life without transcriptional control? from fly to man and back again (2002) EMBO J, 21, pp. 1881-1888
  • Sutton, R.E., Boothroyd, J.C., Evidence for trans-splicing in trypanosomes (1986) Cell, 47, pp. 527-535
  • Lebowitz, J.H., Smith, H.Q., Rusche, L., Beverley, M., Coupling of poly (A) site selection and trans-splicing in Leishmania (1993) Genes Dev, 7, pp. 996-1007
  • Matthews, K.R., Tschudi, C., Ullu, E., A common pyrimidine-rich motif governs trans-splicing and polyadenylation of tubulin polycistronic pre-mRNA in trypanosomes (1994) Genes Dev, 8, pp. 491-501
  • Vasella, E., Braun, E., Roditi, I., Control of polyadenylation and alternative splicing of transcripts from adjacent genes in procyclic expression site: A dual role for polypirimidine tracts in trypanosomes? (1994) Nucleic Acids Res, 22, pp. 1359-1364
  • Hartmann, C., Hotz, H.R., McAndrew, M., Clayton, C., Effect of multiple downstream splice sites on polyadenylation in Trypanosoma brucei (1998) Mol Biochem Parasitol, 93, pp. 149-152
  • Patzelt, E., Perry, K., Agabian, N., Mapping of branch sites in trans-spliced pre-mRNAs of Trypanosoma brucei (1989) Mol Cell Biol, 9, pp. 4291-4297
  • Hummel, H.S., Gilleespie, D.R., Swindle, J., Mutational analyses of 3′ splice site selection during trans-splicing (2000) J Biol Chem, 275, pp. 35522-35531
  • Ullu, E., Tschudi, C., Günzl, A., Trans-splicing in trypanosomatid protozoa (1996) Frontiers in Molecular Biology: Molecular Biology of Parasitic Protozoa, pp. 115-133. , D.F. Smith M. Parsons Oxford
  • Vázquez, M.P., Levin, M.J., Functional analysis of the intergenic regions of TcP2β gene loci allowed the construction of an improved Trypanosoma cruzi vector (1999) Gene, 239, pp. 217-225
  • Darocha, W.D., Otsu, K., Teixeira, S.M., Donelson, J.E., Tests of cytoplasmic RNA interference (RNAi) and construction of a tetracycline-inducible T7 promoter system in Trypanosoma cruzi (2004) Mol Biochem Parasitol, 133, pp. 175-186
  • Lorenzi, H.A., Vazquez, M.P., Levin, M.J., Integration of expression vectors into the ribosomal locus of Trypanosoma cruzi (2003) Gene, 310, pp. 91-99
  • Vázquez, M., Schijman, A., Levin, M.J., A short interspersed repetitive element provides a new 3′ acceptor site for trans-splicing in certain ribosomal TcP2β protein genes of Trypanosoma cruzi (1994) Mol Biochem Parasitol, 67, pp. 327-336
  • Vázquez, M., Ben-Dov, C., Lorenzi, H., Moore, T., Schijman, A., Levin, M.J., The short interspersed repetitive element of Trypanosoma cruzi, SIRE, is part of VIPER, an unusual retroelement related to long terminal repeat retrotransposons (2000) Proc Natl Acad Sci USA, 97, pp. 2128-2133
  • Ho, S.N., Hunt, H.D., Horton, R.M., Pullen, J.K., Pease, L.R., Site directed mutagenesis by overlap extension using polymerase chain reaction (1989) Gene, 77, pp. 51-59
  • Drozdz, M., Clayton, C., Structure of a regulatory 3′ untranslated region from Trypanosoma brucei (1999) RNA, 5, pp. 1632-1644
  • Burge, C.B., Tuschl, T.H., Sharp, P.A., Splicing of precursors to mRNA by the spliceosomes (1999) The RNA World, pp. 525-560. , R.F. Gesteland T.R. Cech J.F. Atkins 2nd ed. Cold Spring Harbor Laboratory Press
  • Vázquez, M., Atorrasagasti, C., Bercovich, N., Volcovich, R., Levin, M.J., Unique features of the Trypanosoma cruzi U2AF35 splicing factor (2003) Mol Biochem Parasitol, 128 (1), pp. 77-81
  • López-Estranio, C., Tschudi, C., Ullu, E., Exonic sequences in the 5′ untranslated region of α-tubulin mRNA modulate trans-splicing in Trypanosoma brucei (1998) Mol Cell Biol, 8, pp. 4620-4628

Citas:

---------- APA ----------
Ben-Dov, C.P., Levin, M.J. & Vázquez, M.P. (2005) . Analysis of the highly efficient pre-mRNA processing region HX1 of Trypanosoma cruzi. Molecular and Biochemical Parasitology, 140(1), 97-105.
http://dx.doi.org/10.1016/j.molbiopara.2005.01.001
---------- CHICAGO ----------
Ben-Dov, C.P., Levin, M.J., Vázquez, M.P. "Analysis of the highly efficient pre-mRNA processing region HX1 of Trypanosoma cruzi" . Molecular and Biochemical Parasitology 140, no. 1 (2005) : 97-105.
http://dx.doi.org/10.1016/j.molbiopara.2005.01.001
---------- MLA ----------
Ben-Dov, C.P., Levin, M.J., Vázquez, M.P. "Analysis of the highly efficient pre-mRNA processing region HX1 of Trypanosoma cruzi" . Molecular and Biochemical Parasitology, vol. 140, no. 1, 2005, pp. 97-105.
http://dx.doi.org/10.1016/j.molbiopara.2005.01.001
---------- VANCOUVER ----------
Ben-Dov, C.P., Levin, M.J., Vázquez, M.P. Analysis of the highly efficient pre-mRNA processing region HX1 of Trypanosoma cruzi. Mol. Biochem. Parasitol. 2005;140(1):97-105.
http://dx.doi.org/10.1016/j.molbiopara.2005.01.001