Analysis of the human SOX10 mutation Q377X in mice and its implications for genotype-phenotype correlation in SOX10-related human disease

Truch, Kathrin and Arter, Juliane and Turnescu, Tanja and Weider, Matthias and Hartwig, Anna C. and Tamm, Ernst R. and Sock, Elisabeth and Wegner, Michael (2018) Analysis of the human SOX10 mutation Q377X in mice and its implications for genotype-phenotype correlation in SOX10-related human disease. HUMAN MOLECULAR GENETICS, 27 (6). pp. 1078-1092. ISSN 0964-6906, 1460-2083

Full text not available from this repository. (Request a copy)

Abstract

Human SOX10 mutations lead to various diseases including Waardenburg syndrome, Hirschsprung disease, peripheral demyelinating neuropathy, central leukodystrophy, Kallmann syndrome and various combinations thereof. It has been postulated that PCWH as a combination of Waardenburg and Hirschsprung disease, peripheral neuropathy and central leukodystrophy is caused by heterozygous SOX10 mutations that result in the presence of a dominantly acting mutant SOX10 protein in the patient. One such protein with postulated dominant action is SOX10 Q377X. In this study, we generated a mouse model, in which the corresponding mutation was introduced into the Sox10 locus in such a way that Sox10 Q377X is constitutively expressed. Heterozygous mice carrying this mutation exhibited pigmentation and enteric nervous system defects similar to mice in which one Sox10 allele was deleted. However, despite presence of the mutant protein in Schwann cells and oligodendrocytes throughout development and in the adult, we found no phenotypic evidence for neurological defects in peripheral or central nervous systems. In the nervous system, the mutant Sox10 protein did not act in a dominant fashion but rather behaved like a hypomorph with very limited residual function. Our results question a strict genotype-phenotype correlation for SOX10 mutations and argue for the influence of additional factors including genetic background.

Item Type: Article
Uncontrolled Keywords: TRANSCRIPTION FACTOR SOX10; NEURAL CREST DEVELOPMENT; HIRSCHSPRUNG-DISEASE; MOUSE MODEL; GENE-EXPRESSION; SPINAL-CORD; CELLS; DIFFERENTIATION; CONSEQUENCES; DOMAIN;
Subjects: 500 Science > 570 Life sciences
Divisions: Biology, Preclinical Medicine > Institut für Anatomie > Lehrstuhl für Humananatomie und Embryologie > Prof. Dr. Ernst Tamm
Depositing User: Dr. Gernot Deinzer
Date Deposited: 20 Mar 2020 10:13
Last Modified: 20 Mar 2020 10:13
URI: https://pred.uni-regensburg.de/id/eprint/14891

Actions (login required)

View Item View Item