dc.creatorNajle, Sebastián Rodrigo
dc.creatorHernandez, Josefina
dc.creatorOcaña Pallarès, Eduard
dc.creatorGarcía Siburu, Nicolás Pablo
dc.creatorNusblat, Alejandro David
dc.creatorNudel, Berta Clara
dc.creatorSlamovits, Claudio H.
dc.creatorUttaro, Antonio Domingo
dc.date.accessioned2022-02-22T00:14:49Z
dc.date.accessioned2022-10-15T02:27:08Z
dc.date.available2022-02-22T00:14:49Z
dc.date.available2022-10-15T02:27:08Z
dc.date.created2022-02-22T00:14:49Z
dc.date.issued2020-03
dc.identifierNajle, Sebastián Rodrigo; Hernandez, Josefina; Ocaña Pallarès, Eduard; García Siburu, Nicolás Pablo; Nusblat, Alejandro David; et al.; Genome-wide Transcriptional Analysis of Tetrahymena thermophila Response to Exogenous Cholesterol; Wiley Blackwell Publishing, Inc; Journal of Eukaryotic Microbiology; 67; 2; 3-2020; 209-222
dc.identifier1066-5234
dc.identifierhttp://hdl.handle.net/11336/152434
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4335009
dc.description.abstractThe ciliate Tetrahymena thermophila does not require sterols for growth and synthesizes pentacyclic triterpenoid alcohols, mainly tetrahymanol, as sterol surrogates. However, when sterols are present in the environment, T. thermophila efficiently incorporates and modifies them. These modifications consist of desaturation reactions at positions C5(6), C7(8), and C22(23), and de-ethylation at C24 of 29-carbon sterols (i.e. phytosterols). Three out of four of the enzymes involved in the sterol modification pathway have been previously identified. However, identification of the sterol C22 desaturase remained elusive, as did other basic aspects of this metabolism. To get more insights into this peculiar metabolism, we here perform a whole transcriptome analysis of T. thermophila in response to exogenous cholesterol. We found 356 T. thermophila genes to be differentially expressed after supplementation with cholesterol for 2 h. Among those that were upregulated, we found two genes belonging to the long spacing family of desaturases that we tentatively identified by RNAi analysis as sterol C22 desaturases. Additionally, we determined that the inhibition of tetrahymanol synthesis after supplementation with cholesterol occurs by a transcriptional downregulation of genes involved in squalene synthesis and cyclization. Finally, we identified several uncharacterized genes that are likely involved in sterols transport and signaling.
dc.languageeng
dc.publisherWiley Blackwell Publishing, Inc
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1111/jeu.12774
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1111/jeu.12774
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCILIATE
dc.subjectRNA INTERFERENCE
dc.subjectRNA SEQUENCING
dc.subjectSTEROL C22 DESATURASE
dc.subjectSTEROLS METABOLISM
dc.subjectTETRAHYMANOL BIOSYNTHESIS
dc.titleGenome-wide Transcriptional Analysis of Tetrahymena thermophila Response to Exogenous Cholesterol
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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