Please use this identifier to cite or link to this item: http://hdl.handle.net/10662/7274
Title: Alu retrotransposons promote differentiation of human carcinoma cells through the aryl hydrocarbon receptor
Authors: Morales Hernández, Antonio
González Rico, Francisco Javier
Román García, Ángel Carlos
Rico Leo, Eva María
Álvarez Barrientos, Alberto
Sánchez Ruiz, Laura
Macia Ortega, Ángela
Rodríguez Heras, Sara
García Pérez, José Luis
Merino Fernández, Jaime María
Fernández Salguero, Pedro María
CSIC-Instituto Cajal. Madrid
Universidad de Extremadura. Departamento de Bioquímica, Biología Molecular y Genética
Universidad de Granada
Keywords: Diferenciación celular
Regulación de genes
Células de carcinoma
Elementos discretos de Alu
Cell differentiation
Gene regulation
Carcinoma cells
Discrete Alu elements
Issue Date: 2016
Abstract: Cell differentiation is a central process in development and in cancer growth and dissemination. OCT4 (POU5F1) and NANOG are essential for cell stemness and pluripotency; yet, the mechanisms that regulate their expression remain largely unknown. Repetitive elements account for almost half of the Human Genome; still, their role in gene regulation is poorly understood. Here, we show that the dioxin receptor (AHR) leads to differentiation of human carcinoma cells through the transcriptional upregulation of Alu retrotransposons, whose RNA transcripts can repress pluripotency genes. Despite the genome-wide presence of Alu elements, we provide evidences that those located at the NANOG and OCT4 promoters bind AHR, are transcribed by RNA polymerase-III and repress NANOG and OCT4 in differentiated cells. OCT4 and NANOG repression likely involves processing of Alu-derived transcripts through the miRNA machinery involving the Microprocessor and RISC. Consistently, stable AHR knockdown led to basal undifferentiation, impaired Alus transcription and blockade of OCT4 and NANOG repression. We suggest that transcripts produced from AHR-regulated Alu retrotransposons may control the expression of stemness genes OCT4 and NANOG during differentiation of carcinoma cells. The control of discrete Alu elements by specific transcription factors may have a dynamic role in genome regulation under physiological and diseased conditions.
URI: http://hdl.handle.net/10662/7274
ISSN: 0305-1048
Appears in Collections:DBYBM - Artículos

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