Fine-tuning multiciliated cell differentiation at the post-transcriptional level: contribution of miR-34/449 family members

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3009133 7 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Fine-tuning multiciliated cell differentiation at the post-transcriptional level: contribution of miR-34/449 family members
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Cell differentiation is a process that must be precisely regulated for the maintenance of tissue homeostasis. Differentiation towards a multiciliated cell fate is characterized by well-defined stages, where a transcriptional cascade is activated leading to the formation of multiple centrioles and cilia. Centrioles migrate and dock to the apical cell surface and, acting as basal bodies, give rise to multiple motile cilia. The concerted movement of cilia ensures directional fluid flow across epithelia and defects either in their number or structure can lead to disease phenotypes. Micro-RNAs (miRNAs; miRs) are small, non-coding RNA molecules that play an important role in post-transcriptional regulation of gene expression. miR-34b/c and miR-449a/b/c specifically function throughout the differentiation of multiciliated cells, fine-tuning the expression of many different centriole- and cilia-related genes. They strictly regulate the expression levels of genes that are required both for commitment towards the multiciliated cell fate (e.g. Notch) and for the establishment and maintenance of this fate by regulating the expression of transcription factors and structural components of the pathway. Herein we review miR-34 and miR-449 spatiotemporal regulation along with their roles during the different stages of multiciliogenesis. © 2021 Cambridge Philosophical Society.
Έτος δημοσίευσης:
2021
Συγγραφείς:
Loukas, I.
Skamnelou, M.
Tsaridou, S.
Bournaka, S.
Grigoriadis, S.
Taraviras, S.
Lygerou, Z.
Arbi, M.
Περιοδικό:
Fungal Biology Reviews
Εκδότης:
John Wiley and Sons Inc
Τόμος:
96
Αριθμός / τεύχος:
5
Σελίδες:
2321-2332
Επίσημο URL (Εκδότης):
DOI:
10.1111/brv.12755
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.