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Genetic variation in CFTR and modifier loci may modulate cystic fibrosis disease severity
- Source :
- Journal of Cystic Fibrosis, Journal of Cystic Fibrosis, Elsevier, 2020, 19, pp.S10-S14. ⟨10.1016/j.jcf.2019.11.001⟩, J Cyst Fibros
- Publication Year :
- 2020
- Publisher :
- HAL CCSD, 2020.
-
Abstract
- In patients with cystic fibrosis (CF), genetic variants within and outside the CFTR locus contribute to the variability of the disease severity. CFTR transcription is tightly regulated by cis-regulatory elements (CREs) that control the three-dimensional structure of the locus, chromatin accessibility and transcription factor recruitment. Variants within these CREs may contribute to the pathophysiology and to the phenotypic heterogeneity by altering CFTR transcript abundance. In addition to the CREs, variants outside the CFTR locus, namely "modifiers genes", may also be associated with the clinical variability. This review addresses variants at the CFTR locus itself and CFTR CREs, together with the outcomes of the latest modifier gene studies with respect to the different CF phenotypes.
- Subjects :
- 0301 basic medicine
Pulmonary and Respiratory Medicine
congenital, hereditary, and neonatal diseases and abnormalities
Cystic Fibrosis
[SDV]Life Sciences [q-bio]
Cystic Fibrosis Transmembrane Conductance Regulator
Locus (genetics)
Cystic fibrosis
Severity of Illness Index
Article
03 medical and health sciences
0302 clinical medicine
Genetic variation
Medicine
Humans
Gene
Transcription factor
Genetic Association Studies
Genetics
Genes, Modifier
business.industry
Genetic heterogeneity
Genetic Variation
respiratory system
medicine.disease
Phenotype
digestive system diseases
Chromatin
respiratory tract diseases
030104 developmental biology
030228 respiratory system
Pediatrics, Perinatology and Child Health
business
Subjects
Details
- Language :
- English
- ISSN :
- 15691993
- Database :
- OpenAIRE
- Journal :
- Journal of Cystic Fibrosis, Journal of Cystic Fibrosis, Elsevier, 2020, 19, pp.S10-S14. ⟨10.1016/j.jcf.2019.11.001⟩, J Cyst Fibros
- Accession number :
- edsair.doi.dedup.....f9150548cace8327eb9ccdc56a9317aa
- Full Text :
- https://doi.org/10.1016/j.jcf.2019.11.001⟩