The gene regulatory capacity and diversity of microRNAs (miRNAs) is critical in the central nervous system where constant and rapid adaptation to environmental changes is needed, both during development and in the adult. Here, we will discuss how miRNA biogenesis is modulated to sustain a variety of neural phenomena, including embryonic and adult neurogenesis. Moreover, we will present the newly discovered miRNA-independent function of the microprocessor where mRNA regulation is achieved through direct site-specific cleavage by the RNAse III Drosha. Noncanonical functions of the microprocessor have striking effects on neural stem cells (NSCs), directly repressing the stability of mRNAs that encode proteins crucial for stem cell activity. We will discuss and compare different mechanisms through which the microprocessor regulates NSC maintenance and differentiation during embryonic and adult neurogenesis.

miRNA-Dependent and Independent Functions of the Microprocessor in the Regulation of Neural Stem Cell Biology / A. Erni, C. Rolando, V. Taylor - In: Essentials of Noncoding RNA in Neuroscience : Ontogenetics, Plasticity of the Vertebrate Brain / [a cura di] D. De Pietri Tonelli. - [s.l] : Academic Press, 2017 Aug. - ISBN 9780128044025. - pp. 101-117 [10.1016/B978-0-12-804402-5.00006-6]

miRNA-Dependent and Independent Functions of the Microprocessor in the Regulation of Neural Stem Cell Biology

C. Rolando;
2017

Abstract

The gene regulatory capacity and diversity of microRNAs (miRNAs) is critical in the central nervous system where constant and rapid adaptation to environmental changes is needed, both during development and in the adult. Here, we will discuss how miRNA biogenesis is modulated to sustain a variety of neural phenomena, including embryonic and adult neurogenesis. Moreover, we will present the newly discovered miRNA-independent function of the microprocessor where mRNA regulation is achieved through direct site-specific cleavage by the RNAse III Drosha. Noncanonical functions of the microprocessor have striking effects on neural stem cells (NSCs), directly repressing the stability of mRNAs that encode proteins crucial for stem cell activity. We will discuss and compare different mechanisms through which the microprocessor regulates NSC maintenance and differentiation during embryonic and adult neurogenesis.
Nuclear receptor TLX; epigenetic regulation; messenger-RNA; subventricular zone; neuronal migration; target recognition; conditional loss; in-vivo; microRna; drosha
Settore BIO/06 - Anatomia Comparata e Citologia
Settore BIO/16 - Anatomia Umana
ago-2017
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/705647
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