Literature DB >> 33677604

The Impact of Environmental Factors on Monogenic Mendelian Diseases.

Anke M Tukker1, Charmaine D Royal2, Aaron B Bowman1, Kimberly A McAllister3.   

Abstract

Environmental factors and gene-environment interactions modify the variable expressivity, progression, severity, and onset of some classic (monogenic) Mendelian-inherited genetic diseases. Cystic fibrosis, Huntington disease, Parkinson's disease, and sickle cell disease are examples of well-known Mendelian disorders that are influenced by exogenous exposures. Environmental factors may act by direct or indirect mechanisms to modify disease severity, timing, and presentation, including through epigenomic influences, protein misfolding, miRNA alterations, transporter activity, and mitochondrial effects. Because pathological features of early-onset Mendelian diseases can mimic later onset complex diseases, we propose that studies of environmental exposure vulnerabilities using monogenic model systems of rare Mendelian diseases have high potential to provide insight into complex disease phenotypes arising from multi-genetic/multi-toxicant interactions. Mendelian disorders can be modeled by homologous mutations in animal model systems with strong recapitulation of human disease etiology and natural history, providing an important advantage for study of these diseases. Monogenic high penetrant mutations are ideal for toxicant challenge studies with a wide variety of environmental stressors, because background genetic variability may be less able to alter the relatively strong phenotype driving disease-causing mutations. These models promote mechanistic understandings of gene-environment interactions and biological pathways relevant to both Mendelian and related sporadic complex disease outcomes by creating a sensitized background for relevant environmental risk factors. Additionally, rare disease communities are motivated research participants, creating the potential of strong research allies among rare Mendelian disease advocacy groups and disease registries and providing a variety of translational opportunities that are under-utilized in genetic or environmental health science. Published by Oxford University Press on behalf of the Society of Toxicology 2021. This work is written by a US Government employee and is in the public domain in the US.

Entities:  

Keywords:  cystic fibrosis; gene-environment interactions; huntington disease; monogenic mendelian diseases; parkinson’s disease; sickle cell disease

Year:  2021        PMID: 33677604     DOI: 10.1093/toxsci/kfab022

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  2 in total

1.  Compound Heterozygous COX20 Variants Impair the Function of Mitochondrial Complex IV to Cause a Syndrome Involving Ophthalmoplegia and Visual Failure.

Authors:  Peizheng Li; Dandan Guo; Xiufang Zhang; Kunqian Ji; Hongbo Lv; Yanli Zhang; Zhichao Chen; Jun Ma; Yaofeng Fang; Yiming Liu
Journal:  Front Neurol       Date:  2022-05-16       Impact factor: 4.086

Review 2.  Incomplete Penetrance and Variable Expressivity: From Clinical Studies to Population Cohorts.

Authors:  Rebecca Kingdom; Caroline F Wright
Journal:  Front Genet       Date:  2022-07-25       Impact factor: 4.772

  2 in total

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