Chromothripsis and DNA Repair Disorders.
Ontology highlight
ABSTRACT: Chromothripsis is a mutational mechanism leading to complex and relatively clustered chromosomal rearrangements, resulting in diverse phenotypic outcomes depending on the involved genomic landscapes. It may occur both in the germ and the somatic cells, resulting in congenital and developmental disorders and cancer, respectively. Asymptomatic individuals may be carriers of chromotriptic rearrangements and experience recurrent reproductive failures when two or more chromosomes are involved. Several mechanisms are postulated to underlie chromothripsis. The most attractive hypothesis involves chromosome pulverization in micronuclei, followed by the incorrect reassembly of fragments through DNA repair to explain the clustered nature of the observed complex rearrangements. Moreover, exogenous or
SUBMITTER: Nazaryan-Petersen L
PROVIDER: S-EPMC7141117 | biostudies-literature | 2020 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA