Your browser doesn't support javascript.
loading
Canalization and Robustness in Human Genetics and Disease.
Gibson, Greg; Lacek, Kristine A.
Afiliación
  • Gibson G; School of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia 30332, USA; email: greg.gibson@biology.gatech.edu.
  • Lacek KA; School of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia 30332, USA; email: greg.gibson@biology.gatech.edu.
Annu Rev Genet ; 54: 189-211, 2020 11 23.
Article en En | MEDLINE | ID: mdl-32867542
ABSTRACT
Canalization refers to the evolution of populations such that the number of individuals who deviate from the optimum trait, or experience disease, is minimized. In the presence of rapid cultural, environmental, or genetic change, the reverse process of decanalization may contribute to observed increases in disease prevalence. This review starts by defining relevant concepts, drawing distinctions between the canalization of populations and robustness of individuals. It then considers evidence pertaining to three continuous traits and six domains of disease. In each case, existing genetic evidence for genotype-by-environment interactions is insufficient to support a strong inference of decanalization, but we argue that the advent of genome-wide polygenic risk assessment now makes an empirical evaluation of the role of canalization in preventing disease possible. Finally, the contributions of both rare and common variants to congenital abnormality and adult onset disease are considered in light of a new kerplunk model of genetic effects.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma / Genética Humana / Enfermedades Genéticas Congénitas Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Annu Rev Genet Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Genoma / Genética Humana / Enfermedades Genéticas Congénitas Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Annu Rev Genet Año: 2020 Tipo del documento: Article