Measuring FOXO Activity by Using qPCR-Based Expression Analysis of FOXO Target Genes.

Autor:	Jimenez L; Sols-Morreale Biomedical Research Institute (IIBM), Spanish National Research Council (CSIC), Universidad Autónoma de Madrid (UAM), Madrid, Spain., Grenho I; ABC-Ri, Algarve Biomedical Center Research Institute, Algarve Biomedical Center, Faro, Portugal.; Faculty of Medicine and Biomedical Sciences, University of Algarve, Faro, Portugal., Santos B; ABC-Ri, Algarve Biomedical Center Research Institute, Algarve Biomedical Center, Faro, Portugal.; Faculty of Medicine and Biomedical Sciences, University of Algarve, Faro, Portugal., Serrão G; ABC-Ri, Algarve Biomedical Center Research Institute, Algarve Biomedical Center, Faro, Portugal.; Faculty of Medicine and Biomedical Sciences, University of Algarve, Faro, Portugal., Mayoral-Varo V; Facultad HM Hospitales de Ciencias de la Salud de la Universidad Camilo José Cela, Madrid, Spain., Link W; Department of Cancer Biology, Sols-Morreale Biomedical Research Institute (IIBM), Spanish National Research Council (CSIC), Universidad Autónoma de Madrid (UAM), Madrid, Spain., Ferreira BI; ABC-Ri, Algarve Biomedical Center Research Institute, Algarve Biomedical Center, Faro, Portugal. biferreira@ualg.pt.; Faculty of Medicine and Biomedical Sciences, University of Algarve, Faro, Portugal. biferreira@ualg.pt.
Jazyk:	angličtina
Zdroj:	Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2025; Vol. 2871, pp. 33-43.
DOI:	10.1007/978-1-0716-4217-7_4
Abstrakt:	FOXO transcription factors belong to the forkhead protein family and are distinguished by their unique forkhead (FKH) DNA-binding domain. In the realm of mammals, four FOXO paralogs are recognized: FOXO1, FOXO3, FOXO4, and FOXO6. These paralogs are evolutionary counterparts of the daf-16 gene discovered in the nematode C. elegans. A key feature shared by these paralogs is a consensus binding site known as the DAF-16 family protein-binding site (DBE: 5'-TTGTTTAC-3'). The functional outcome of FOXO transcription factors primarily hinges on their affinity for these specific binding sites within the promoters of their target genes. Nevertheless, it is worth noting that many of these target genes exhibit tissue-specific expression patterns. Consequently, there is not a single FOXO target gene whose expression can reliably serve as a universal indicator of FOXO activity across all cell types and tissues or in response to all stimuli. In light of these considerations, we present a collection of target genes that, when collectively assessed, can accurately gauge FOXO activation. In this chapter, we outline a specific protocol for utilizing quantitative reverse transcription polymerase chain reaction (qRT-PCR) to measure the expression levels of these genes. (© 2025. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.)
Databáze:	MEDLINE
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