Genetic Variants in Transcription Factor Binding Sites in Humans: Triggered by Natural Selection and Triggers of Diseases.
Chia-Chun TsengMan-Chun WongWei-Ting LiaoChung-Jen ChenSu-Chen LeeJeng-Hsien YenShun-Jen ChangPublished in: International journal of molecular sciences (2021)
Variants of transcription factor binding sites (TFBSs) constitute an important part of the human genome. Current evidence demonstrates close links between nucleotides within TFBSs and gene expression. There are multiple pathways through which genomic sequences located in TFBSs regulate gene expression, and recent genome-wide association studies have shown the biological significance of TFBS variation in human phenotypes. However, numerous challenges remain in the study of TFBS polymorphisms. This article aims to cover the current state of understanding as regards the genomic features of TFBSs and TFBS variants; the mechanisms through which TFBS variants regulate gene expression; the approaches to studying the effects of nucleotide changes that create or disrupt TFBSs; the challenges faced in studies of TFBS sequence variations; the effects of natural selection on collections of TFBSs; in addition to the insights gained from the study of TFBS alleles related to gout, its associated comorbidities (increased body mass index, chronic kidney disease, diabetes, dyslipidemia, coronary artery disease, ischemic heart disease, hypertension, hyperuricemia, osteoporosis, and prostate cancer), and the treatment responses of patients.
Keyphrases
- gene expression
- copy number
- chronic kidney disease
- end stage renal disease
- transcription factor
- prostate cancer
- coronary artery disease
- endothelial cells
- body mass index
- dna methylation
- type diabetes
- blood pressure
- cardiovascular disease
- genome wide association
- newly diagnosed
- pluripotent stem cells
- metabolic syndrome
- heart failure
- peritoneal dialysis
- ejection fraction
- physical activity
- cardiovascular events
- amino acid
- percutaneous coronary intervention
- genome wide identification
- left ventricular
- transcatheter aortic valve replacement
- replacement therapy