Abstract

Trypanosoma cruzi, the agent of Chagas disease, does not seem to control gene expression through regulation of transcription initiation and makes use of post-transcriptional mechanisms. We report here a 43-nt U-rich RNA element located in the 3'-untranslated region (3'-UTR) of a large number of T. cruzi mRNAs that is important for mRNA abundance in the intracellular amastigote stage of the parasite. Whole genome scan analysis, differential display RT-PCR, Northern blot, and RT-PCR analyses were used to determine the transcript levels of more than 900 U-rich-containing mRNAs of large gene families as well as single and low copy number genes. Our results indicate that the 43-nt U-rich mRNA element is preferentially present in amastigotes. The cis-element of a protein kinase 3'-UTR but not its mutated version promoted the expression of the green fluorescent protein reporter gene in amastigotes. The regulatory cis-element, but not its mutated version, was also shown to interact with the trypanosome-specific RNA-binding protein (RBP) TcUBP1 but not with other related RBPs. Co-immunoprecipitation experiments of TcUBP1-containing ribonucleoprotein complexes formed in vivo validated the interaction with representative endogenous RNAs having the element. These results suggest that this 43-nt U-rich element together with other yet unidentified sequences might be involved in the modulation of abundance and/or translation of subsets of transcripts in the amastigote stage.

Highlights

  • Trypanosoma cruzi regulates gene expression by means of post-transcriptional mechanisms

  • We report here a 43-nt U-rich RNA element located in the 3؅-untranslated region (3؅-untranslated regions (UTRs)) of a large number of T. cruzi mRNAs that is important for mRNA abundance in the intracellular amastigote stage of the parasite

  • This cis-element, but not its mutated version, was shown to interact with the trypanosome-specific factor TcUBP1. These results suggest that messenger ribonucleoprotein complexes containing this 43-nt RNA element could act as a post-transcriptional regulon in the amastigote stages of the parasite

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Summary

Background

Trypanosoma cruzi regulates gene expression by means of post-transcriptional mechanisms. It has been reported that multiple mRNAs can be co-regulated by one or more sequence-specific RBPs that orchestrate their splicing, export, stability, localization, and translation [13,14,15,16] The existence of these post-transcriptional regulons would be a very appropriate mechanism for the developmental regulation of gene expression in trypanosomatids. The list of developmentally regulated transcripts includes more than 900 mRNAs of large gene families (trans-sialidase (TS), mucin-associated protein (MASP), mucin, surface protease GP63, and protein kinase) as well as single or low copy number genes This cis-element, but not its mutated version, was shown to interact with the trypanosome-specific factor TcUBP1. These results suggest that messenger ribonucleoprotein (mRNP) complexes containing this 43-nt RNA element could act as a post-transcriptional regulon in the amastigote stages of the parasite

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