A short RNA stem–loop is necessary and sufficient for repression of gene expression during early logarithmic phase in trypanosomes
Fecha de publicación
2014ISSN
1362-4962
Resumen
We have compared the transcriptomes of cultured procyclic Trypanosoma brucei cells in early and late logarithmic phases and found that ∼200 mRNAs were differentially regulated. In late log phase cells, the most upregulated mRNA encoded the nucleobase transporter NT8. The 3′ untranslated region (UTR) of NT8 contains a short stem–loop cis-element that is necessary for the regulation of NT8 expression in response to external purine levels. When placed in the 3′-UTR of an unregulated transcript, the cis-element is sufficient to confer regulation in response to purines. To our knowledge, this is the first example of a discrete RNA element that can autonomously regulate gene expression in trypanosomes in response to an external factor and reveals an unprecedented purine-dependent signaling pathway that controls gene expression in eukaryotes.
Tipo de documento
Artículo
Versión del documento
Versión publicada
Lengua
Inglés
Materias (CDU)
61 - Medicina
Páginas
8
Publicado por
Nucleic Acids Research
Colección
42; 11
Publicado en
Nucleic Acids Research
Citación
Fernández-Moya, Sandra M.; Carrington, Mark; Estévez, Antonio M. [et al.]. A short RNA stem–loop is necessary and sufficient for repression of gene expression during early logarithmic phase in trypanosomes. Nucleic Acids Research, 2014, 42(11), p. 7201-7209. Disponible en: <https://academic.oup.com/nar/article/42/11/7201/1444696?login=false>. Fecha de acceso: 24 ene. 2025. DOI: 10.1093/nar/gku358
Nota
Ministerio de Ciencia e Innovación [BFU 2009-07510 to A.M.E.]; The Wellcome Trust [085956 to M.C.]; The Royal Society Joint Project [2008/R2 to M.C. and A.M.E.]. Funding for open access charge: The Wellcome Trust.
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© This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
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