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miRNA let-7 expression is regulated by glucose and TNF-α by a remote upstream promoter.
- Source :
-
The Biochemical journal [Biochem J] 2015 Dec 01; Vol. 472 (2), pp. 147-56. Date of Electronic Publication: 2015 Sep 16. - Publication Year :
- 2015
-
Abstract
- miRNAs regulate protein abundance and control diverse aspects of cellular processes and biological functions in metabolic diseases, such as obesity and type 2 diabetes (T2D). Let (lethal)-7 miRNAs specifically targets genes associated with T2D and have been implicated in the regulation of peripheral glucose metabolism, yet the direct regulators of let-7 miRNA expression are unknown. In the present study, we report on a putative promoter region for the let-7a-1, let-7f-1 and let-7d gene cluster on chromosome 9 and characterize the promoter activity of this novel area. We show that promoter activity and let-7 miRNA expression is dynamically regulated in response to different factors including serum, glucose, tumour necrosis factor (TNF)-α and caffeine. These findings will contribute to understanding the interaction between precise promoter elements to control the transcription and translation of let-7 miRNA genes.<br /> (© 2015 Authors; published by Portland Press Limited.)
- Subjects :
- Blood Glucose metabolism
Cells, Cultured
Chromosomes, Human, Pair 9
Computational Biology
Databases, Nucleic Acid
Genes, Reporter
Genome, Human
HEK293 Cells
Humans
Hyperglycemia blood
Hyperglycemia metabolism
MicroRNAs metabolism
Multigene Family
Osmolar Concentration
RNA, Messenger metabolism
Recombinant Proteins metabolism
Transfection
Tumor Necrosis Factor-alpha genetics
Caffeine metabolism
Gene Expression Regulation
Glucose metabolism
MicroRNAs agonists
Promoter Regions, Genetic
Satellite Cells, Skeletal Muscle metabolism
Tumor Necrosis Factor-alpha metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1470-8728
- Volume :
- 472
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- The Biochemical journal
- Publication Type :
- Academic Journal
- Accession number :
- 26378151
- Full Text :
- https://doi.org/10.1042/BJ20150224