Psychiatric disorders are known to result from a strong interaction between genetic predisposition and environmental factors, mainly exposure to stressful events. Environmental events can modulate genes expression, possibly via epigenetic mechanisms, and affect onset/expression of a disease [1]. Epigenetic mechanisms include, among others, post-transcriptional regulation by non-coding RNAs such as microRNAs (miRNAs). MiRNAs are small non-coding RNAs predicted to regulate hundreds of targets and to be engaged in every biological process [2]. Thanks to their ability to fine-tune gene expression, miRNAs can control gene expression patterns favoring organism’s adaptation to internal and environmental (external) factors [3], such as stressful events.

MiRNA-34 and stress response / Andolina, Diego; DI SEGNI, Matteo; Ventura, Rossella. - In: ONCOTARGET. - ISSN 1949-2553. - STAMPA. - 4:8(2017), pp. 5658-5659. [10.18632/oncotarget.13923]

MiRNA-34 and stress response

ANDOLINA, DIEGO;DI SEGNI, MATTEO;VENTURA, Rossella
2017

Abstract

Psychiatric disorders are known to result from a strong interaction between genetic predisposition and environmental factors, mainly exposure to stressful events. Environmental events can modulate genes expression, possibly via epigenetic mechanisms, and affect onset/expression of a disease [1]. Epigenetic mechanisms include, among others, post-transcriptional regulation by non-coding RNAs such as microRNAs (miRNAs). MiRNAs are small non-coding RNAs predicted to regulate hundreds of targets and to be engaged in every biological process [2]. Thanks to their ability to fine-tune gene expression, miRNAs can control gene expression patterns favoring organism’s adaptation to internal and environmental (external) factors [3], such as stressful events.
2017
MIR-34; stress response; anxiety; medial prefrontal cortex; amygdala; neuroscience
01 Pubblicazione su rivista::01m Editorial/Introduzione in rivista
MiRNA-34 and stress response / Andolina, Diego; DI SEGNI, Matteo; Ventura, Rossella. - In: ONCOTARGET. - ISSN 1949-2553. - STAMPA. - 4:8(2017), pp. 5658-5659. [10.18632/oncotarget.13923]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/943595
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