SLU7: A New Hub of Gene Expression Regulation-From Epigenetics to Protein Stability in Health and Disease

被引:4
作者
Garate-Rascon, Maria [1 ]
Recalde, Miriam [1 ]
Rojo, Carla [1 ]
Fernandez-Barrena, Maite G. [1 ,2 ,3 ]
Avila, Matias A. [1 ,2 ,3 ]
Arechederra, Maria [1 ,2 ,3 ]
Berasain, Carmen [1 ,2 ,3 ]
机构
[1] Univ Navarra, Program Hepatol, Ctr Appl Med Res CIMA, Avda Pio XII,n55, Pamplona 31008, Spain
[2] Navarra Inst Hlth Res, IdiSNA, Pamplona 31008, Spain
[3] Carlos III Hlth Inst, Natl Inst Study Liver & Gastrointestinal Dis, CIBERehd, Madrid 28029, Spain
关键词
alternative splicing; gene expression; transcription; epigenetics; differentiation; stress; genomic stability; cell cycle; liver pathophysiology; cancer; SISTER-CHROMATID COHESION; SPLICING FACTOR HSLU7; MIR-17-92; CLUSTER; GROWTH-FACTOR; HEPATOCELLULAR-CARCINOMA; OXIDATIVE STRESS; DNA METHYLATION; LIVER-DISEASE; P53; FAMILY; CELL-CYCLE;
D O I
10.3390/ijms232113411
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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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页数:19
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