Pregled bibliografske jedinice broj: 1111177
Molecular map of GNAO1-related disease phenotypes and reactions to therapy
Molecular map of GNAO1-related disease phenotypes and reactions to therapy, 2017. doi:10.1101/232058 (rukopis).
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Naslov
Molecular map of GNAO1-related disease phenotypes and reactions to therapy
Autori
Mihalek, Ivana ; Waugh, Jeff L. ; Park, Meredith ; Kayani, Saima ; Poduri, Annapurna ; Bodamer, Olaf
Izvornik
BioRxiv
Vrsta, podvrsta
Ostale vrste radova, rukopis
Godina
2017
Ključne riječi
GNAO1 ; genotype-phenotype correlation ; molecular basis of disease
Sažetak
The GNAO1 gene codes for the most commonly expressed Gα protein in the central nervous system. Pathogenic GNAO1 variants result in early-onset neurological phenotypes, sometimes with distinct epilepsy or movement disorder, and sometimes with both mani-festations in the same patient. The existing extensive knowledge about G-protein coupled receptor (GPCR) signaling provides the input needed to describe quantitatively how mutations modify the GPCR signal. This in turn allows rational interpretation of distinct phenotypes arising from mutations in GNAO1. In this work we outline a model that enables understanding of clinical phenotypes at a molecular level. The mutations affecting the catalytic pocket of GNAO1, we show, result in the improper withdrawal of the signal, and give rise to epileptic phenotypes (EPs). The converse is not true - some pure EPs are caused by mutations with no obvious impact on catalysis. Mutations close to the interface with GNAO1’s downstream effector block the signal propagation in that direction, and manifest as a movement disorder phenotype without epilepsy. Quantifying the reported reaction to therapy highlights the tendency of the latter group to be unresponsive to the therapies currently in use. We argue, however, that the majority of clinically described mutations can impact several aspects of GNAO1 function at once, resulting in the continuum of phenotypes observed in patients. The reasoning based on GNAO1 signaling model provides a precision medicine paradigm to aid clinicians in selecting effective categories of medication, and in addition, can suggest pragmatic targets for future therapies.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Računarstvo, Interdisciplinarne biotehničke znanosti, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)