Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome.

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License: CC BY 4.0
Serval ID
serval:BIB_D9A4B043FC02
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome.
Journal
Journal of medical genetics
Author(s)
De Nittis P., Efthymiou S., Sarre A., Guex N., Chrast J., Putoux A., Sultan T., Raza Alvi J., Ur Rahman Z., Zafar F., Rana N., Rahman F., Anwar N., Maqbool S., Zaki M.S., Gleeson J.G., Murphy D., Galehdari H., Shariati G., Mazaheri N., Sedaghat A., Lesca G., Chatron N., Salpietro V., Christoforou M., Houlden H., Simonds W.F., Pedrazzini T., Maroofian R., Reymond A.
Working group(s)
SYNAPS Study Group
Contributor(s)
Groppa S., Karashova B.M., Nachbauer W., Boesch S., Arning L., Timmann D., Cormand B., Pérez-Dueñas B., Goraya J.S., Sultan T., Mine J., Avdjieva D., Kathom H., Tincheva R., Banu S., Pineda-Marfa M., Veggiotti P., Ferrari M.D., Maagdenberg AMJMVD, Verrotti A., Marseglia G., Savasta S., García-Silva M., Ruiz A.M., Garavaglia B., Borgione E., Portaro S., Sanchez B.M., Boles R., Papacostas S., Vikelis M., Papanicolaou E.Z., Dardiotis E., Maqbool S., Ibrahim S., Kirmani S., Rana N.N., Atawneh O., Koutsis G., Mangano S., Scuderi C., Borgione E., Morello G., Stojkovic T., Zollo M., Heimer G., Dauvilliers Y.A., Striano P., Al-Khawaja I., Al-Mutairi F., Sherifa H.
ISSN
1468-6244 (Electronic)
ISSN-L
0022-2593
Publication state
Published
Issued date
12/2021
Peer-reviewed
Oui
Volume
58
Number
12
Pages
815-831
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
Pathogenic variants of GNB5 encoding the β <sub>5</sub> subunit of the guanine nucleotide-binding protein cause IDDCA syndrome, an autosomal recessive neurodevelopmental disorder associated with cognitive disability and cardiac arrhythmia, particularly severe bradycardia.
We used echocardiography and telemetric ECG recordings to investigate consequences of Gnb5 loss in mouse.
We delineated a key role of Gnb5 in heart sinus conduction and showed that Gnb5-inhibitory signalling is essential for parasympathetic control of heart rate (HR) and maintenance of the sympathovagal balance. Gnb5 <sup>-/-</sup> mice were smaller and had a smaller heart than Gnb5 <sup>+/+</sup> and Gnb5 <sup>+/-</sup> , but exhibited better cardiac function. Lower autonomic nervous system modulation through diminished parasympathetic control and greater sympathetic regulation resulted in a higher baseline HR in Gnb5 <sup>-/-</sup> mice. In contrast, Gnb5 <sup>-/-</sup> mice exhibited profound bradycardia on treatment with carbachol, while sympathetic modulation of the cardiac stimulation was not altered. Concordantly, transcriptome study pinpointed altered expression of genes involved in cardiac muscle contractility in atria and ventricles of knocked-out mice. Homozygous Gnb5 loss resulted in significantly higher frequencies of sinus arrhythmias. Moreover, we described 13 affected individuals, increasing the IDDCA cohort to 44 patients.
Our data demonstrate that loss of negative regulation of the inhibitory G-protein signalling causes HR perturbations in Gnb5 <sup>-</sup> <sup>/-</sup> mice, an effect mainly driven by impaired parasympathetic activity. We anticipate that unravelling the mechanism of Gnb5 signalling in the autonomic control of the heart will pave the way for future drug screening.
Keywords
GNB5variants, Gnb5-null mouse models, IDDCA, cardiac conduction anomalies, GNB5variants, Gnb5-null mouse models
Pubmed
Web of science
Open Access
Yes
Create date
16/11/2020 14:20
Last modification date
23/11/2022 6:50
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