Gene editing of putative c<scp>AMP</scp> and Ca<sup>2+</sup>‐regulated proteins using an efficient cloning‐free <scp>CRISPR</scp>/Cas9 system in <i>Trypanosoma cruzi</i>
Miguel Ángel Chiurillo, Milad Ahmed, César Antonio González-Díaz, Aqsa Raja, Noelia Lander
Abstract
Abstract Trypanosoma cruzi , the agent of Chagas disease, must adapt to a diversity of environmental conditions that it faces during its life cycle. The adaptation to these changes is mediated by signaling pathways that coordinate the cellular responses to the new environmental settings. Cyclic AMP (cAMP) and Calcium (Ca 2+ ) signaling pathways regulate critical cellular processes in this parasite, such as differentiation, osmoregulation, host cell invasion and cell bioenergetics. Although the use of CRISPR/Cas9 technology prompted reverse genetics approaches for functional analysis in T . cruzi , it is still necessary to expand the toolbox for genome editing in this parasite, as for example to perform multigene analysis. Here we used an efficient T7RNAP/Cas9 strategy to tag and delete three genes predicted to be involved in cAMP and Ca 2+ signaling pathways: a putative Ca 2+ /calmodulin‐dependent protein kinase ( CAMK ), Flagellar Member 6 ( FLAM6 ) and Cyclic nucleotide‐binding domain/C2 domain‐containing protein ( CC2CP ). We endogenously tagged these three genes and determined the subcellular localization of the tagged proteins. Furthermore, the strategy used to knockout these genes allows us to presume that TcCC2CP is an essential gene in T . cruzi epimastigotes. Our results will open new venues for future research on the role of these proteins in T . cruzi .