SLU7: a new hub of gene expression regulation-from epigenetics to protein stability in health and disease
Keywords: 
Alternative splicing
Gene expression
Transcription
Epigenetics
Differentiation
Stress
Genomic stability
Cell cycle
Liver pathophysiology
Cancer
Issue Date: 
2022
ISSN: 
1422-0067
Note: 
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license
Citation: 
Gárate-Rascón, M. (María); Recalde-Domínguez de Vidaurreta, M. (Miriam); Rojo-González, C. (Carla); et al. "SLU7: a new hub of gene expression regulation-from epigenetics to protein stability in health and disease". International Journal of Molecular Sciences. 23 (21), 2022, 13411
Abstract
SLU7 (Splicing factor synergistic lethal with U5 snRNA 7) was first identified as a splicing factor necessary for the correct selection of 3 ' splice sites, strongly impacting on the diversity of gene transcripts in a cell. More recent studies have uncovered new and non-redundant roles of SLU7 as an integrative hub of different levels of gene expression regulation, including epigenetic DNA remodeling, modulation of transcription and protein stability. Here we review those findings, the multiple factors and mechanisms implicated as well as the cellular functions affected. For instance, SLU7 is essential to secure liver differentiation, genome integrity acting at different levels and a correct cell cycle progression. Accordingly, the aberrant expression of SLU7 could be associated with human diseases including cancer, although strikingly, it is an essential survival factor for cancer cells. Finally, we discuss the implications of SLU7 in pathophysiology, with particular emphasis on the progression of liver disease and its possible role as a therapeutic target in human cancer.

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