Brain development involves proliferation, migration and specification of neural progenitor cells, culminating in neuronal circuit formation. Mounting evidence indicates that improper regulation of RNA binding proteins (RBPs), including members of the FET (FUS, EWS, TAF15) family, results in defective cortical development and/or neurodegenerative disorders. However, in spite of their physiological relevance, the precise pattern of FET protein expression in developing neurons is largely unknown. Herein, we found that FUS, EWS and TAF15 expression is differentially regulated during brain development, both in time and in space. In particular, our study identifies a fine-tuned regulation of FUS and EWS during neuronal differentiation, whereas TAF15 appears to be more constitutively expressed. Mechanistically FUS and EWS protein expression is regulated at the post-transcriptional level during neuron differentiation and brain development. Moreover, we identified miR-141 as a key regulator of these FET proteins that modulate their expression levels in differentiating neuronal cells. Thus, our studies uncover a novel link between post-transcriptional regulation of FET proteins expression and neurogenesis.

Post-transcriptional regulation of FUS and EWS protein expression by miR-141 during neural differentiation / Svetoni, Francesca; De Paola, Elisa; La Rosa, Piergiorgio; Mercatelli, Neri; Caporossi, Daniela; Sette, Claudio; Paronetto, Maria Paola. - In: HUMAN MOLECULAR GENETICS ONLINE. - ISSN 1460-2083. - 26:14(2017), pp. 2732-2746. [10.1093/hmg/ddx160]

Post-transcriptional regulation of FUS and EWS protein expression by miR-141 during neural differentiation

La Rosa, Piergiorgio;
2017

Abstract

Brain development involves proliferation, migration and specification of neural progenitor cells, culminating in neuronal circuit formation. Mounting evidence indicates that improper regulation of RNA binding proteins (RBPs), including members of the FET (FUS, EWS, TAF15) family, results in defective cortical development and/or neurodegenerative disorders. However, in spite of their physiological relevance, the precise pattern of FET protein expression in developing neurons is largely unknown. Herein, we found that FUS, EWS and TAF15 expression is differentially regulated during brain development, both in time and in space. In particular, our study identifies a fine-tuned regulation of FUS and EWS during neuronal differentiation, whereas TAF15 appears to be more constitutively expressed. Mechanistically FUS and EWS protein expression is regulated at the post-transcriptional level during neuron differentiation and brain development. Moreover, we identified miR-141 as a key regulator of these FET proteins that modulate their expression levels in differentiating neuronal cells. Thus, our studies uncover a novel link between post-transcriptional regulation of FET proteins expression and neurogenesis.
2017
Animals; Brain; Cell Differentiation; Humans; Mice; Mice, Inbred C57BL; MicroRNAs; Neurogenesis; Neurons; Protein Processing, Post-Translational; RNA-Binding Protein EWS; RNA-Binding Protein FUS; RNA-Binding Proteins; TATA-Binding Protein Associated Factors; RNA Processing, Post-Transcriptional
01 Pubblicazione su rivista::01a Articolo in rivista
Post-transcriptional regulation of FUS and EWS protein expression by miR-141 during neural differentiation / Svetoni, Francesca; De Paola, Elisa; La Rosa, Piergiorgio; Mercatelli, Neri; Caporossi, Daniela; Sette, Claudio; Paronetto, Maria Paola. - In: HUMAN MOLECULAR GENETICS ONLINE. - ISSN 1460-2083. - 26:14(2017), pp. 2732-2746. [10.1093/hmg/ddx160]
File allegati a questo prodotto
File Dimensione Formato  
Svetoni_Post-trascriptional_2017.pdf

accesso aperto

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 1.98 MB
Formato Adobe PDF
1.98 MB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1531327
Citazioni
  • ???jsp.display-item.citation.pmc??? 11
  • Scopus 16
  • ???jsp.display-item.citation.isi??? 14
social impact