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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

CRISPR/Cas9-mediated endogenous C-terminal Tagging of Trypanosoma cruzi Genes Reveals the Acidocalcisome Localization of the Inositol 1,4,5-Trisphosphate Receptor

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Autor(es):
Lander, Noelia ; Chiurillo, Miguel A. ; Storey, Melissa ; Vercesi, Anibal E. ; Docampo, Roberto
Número total de Autores: 5
Tipo de documento: Artigo Científico
Fonte: Journal of Biological Chemistry; v. 291, n. 49, p. 25505-25515, DEC 2 2016.
Citações Web of Science: 27
Resumo

Methods for genetic manipulation of Trypanosoma cruzi, the etiologic agent of Chagas disease, have been highly inefficient, and no endogenous tagging of genes has been reported to date. We report here the use of the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas9 (CRISPR-associated gene 9) system for endogenously tagging genes in this parasite. The utility of the method was established by tagging genes encoding proteins of known localization such as TcFCaBP (flagellar calcium binding protein) and TcVP1 (vacuolar proton pyrophosphatase), and two proteins of undefined or disputed localization, the TcMCU (mitochondrial calcium uniporter) and TcIP3R (inositol 1,4,5-trisphosphate receptor). We confirmed the flagellar and acidocalcisome localization of TcFCaBP and TcVP1 by co-localization with antibodies to the flagellum and acidocalcisomes, respectively. As expected, TcMCU was co-localized with the voltage-dependent anion channel to the mitochondria. However, in contrast to previous reports and our own results using overexpressed TcIP3R, endogenously tagged TcIP3R showed co-localization with antibodies against VP1 to acidocalcisomes. These results are also in agreement with our previous reports on the localization of this channel to acidocalcisomes of Trypanosoma brucei and suggest that caution should be exercised when overexpression of tagged genes is done to localize proteins in T. cruzi. (AU)

Processo FAPESP: 14/08995-4 - Sinalização por íons de cálcio em tripanosomatídeos
Beneficiário:Noelia Marina Lander Manfredi
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
Processo FAPESP: 14/13148-9 - Sinalização por íons de cálcio em tripanossomatídeos
Beneficiário:Miguel Angel Chiurillo Siervo
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado