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Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures

Title: Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures
Authors: Tan, TY; Sedmik, J; Fitzgerald, MP; Halevy, RS; Keegan, LP; Helbig, I; Basel-Salmon, L; Cohen, L; Straussberg, R; Chung, WK; Helal, M; Maroofian, R; Houlden, H; Juusola, J; Sadedin, S; Pais, L; Howell, KB; White, SM; Christodoulou, J; O'Connell, MA
Source: The American Journal of Human Genetics (AJHG) , 106 (4) pp. 467-483. (2020)
Publisher Information: CELL PRESS
Publication Year: 2020
Collection: University College London: UCL Discovery
Subject Terms: Science & Technology; Life Sciences & Biomedicine; Genetics & Heredity; MIGRATING PARTIAL SEIZURES; DYSCHROMATOSIS SYMMETRICA HEREDITARIA; RNA RECOGNITION; BINDING DOMAINS; MICE DEFICIENT; MESSENGER-RNA; INFANCY; GENE; MUTATIONS; ADENOSINE
Description: The RNA editing enzyme ADAR2 is essential for the recoding of brain transcripts. Impaired ADAR2 editing leads to early-onset epilepsy and premature death in a mouse model. Here, we report bi-allelic variants in ADARB1, the gene encoding ADAR2, in four unrelated individuals with microcephaly, intellectual disability, and epilepsy. In one individual, a homozygous variant in one of the double-stranded RNA-binding domains (dsRBDs) was identified. In the others, variants were situated in or around the deaminase domain. To evaluate the effects of these variants on ADAR2 enzymatic activity, we performed in vitro assays with recombinant proteins in HEK293T cells and ex vivo assays with fibroblasts derived from one of the individuals. We demonstrate that these ADAR2 variants lead to reduced editing activity on a known ADAR2 substrate. We also demonstrate that one variant leads to changes in splicing of ADARB1 transcript isoforms. These findings reinforce the importance of RNA editing in brain development and introduce ADARB1 as a genetic etiology in individuals with intellectual disability, microcephaly, and epilepsy.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/10107754/3/Houlden_ADARB1%20submitted%20version.pdf; https://discovery.ucl.ac.uk/id/eprint/10107754/
Availability: https://discovery.ucl.ac.uk/id/eprint/10107754/3/Houlden_ADARB1%20submitted%20version.pdf; https://discovery.ucl.ac.uk/id/eprint/10107754/
Rights: open
Accession Number: edsbas.77037A6E
Database: BASE