4.7 Review

TFEB Signalling-Related MicroRNAs and Autophagy

期刊

BIOMOLECULES
卷 11, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/biom11070985

关键词

TFEB; miRNA; autophagy

资金

  1. AIRC-Associazione Italiana Per la Ricerca sul Cancro [22910]
  2. Regione Piemonte [A1907A]
  3. Fondazione CRT
  4. Ministero dell'Universita e della Ricerca (PRIN 2017) [2017237P5X]
  5. FPRC 5xmille 2016 MIUR (Biofilm)
  6. ERA-Net Transcan-2 [TRS-2018-00000689]

向作者/读者索取更多资源

TFEB, an oncogenic transcription factor, is a key regulator of genes controlling lysosomal biogenesis, autophagy, and vesicle flux. Its activation is modulated by stress factors, with miRNAs playing a role in post-transcriptional regulation. miRNAs are involved in various cellular processes and are important in autophagy.
The oncogenic Transcription Factor EB (TFEB), a member of MITF-TFE family, is known to be the most important regulator of the transcription of genes responsible for the control of lysosomal biogenesis and functions, autophagy, and vesicles flux. TFEB activation occurs in response to stress factors such as nutrient and growth factor deficiency, hypoxia, lysosomal stress, and mitochondrial damage. To reach the final functional status, TFEB is regulated in multimodal ways, including transcriptional rate, post-transcriptional regulation, and post-translational modifications. Post-transcriptional regulation is in part mediated by miRNAs. miRNAs have been linked to many cellular processes involved both in physiology and pathology, such as cell migration, proliferation, differentiation, and apoptosis. miRNAs also play a significant role in autophagy, which exerts a crucial role in cell behaviour during stress or survival responses. In particular, several miRNAs directly recognise TFEB transcript or indirectly regulate its function by targeting accessory molecules or enzymes involved in its post-translational modifications. Moreover, the transcriptional programs triggered by TFEB may be influenced by the miRNA-mediated regulation of TFEB targets. Finally, recent important studies indicate that the transcription of many miRNAs is regulated by TFEB itself. In this review, we describe the interplay between miRNAs with TFEB and focus on how these types of crosstalk affect TFEB activation and cellular functions.

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