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GABRA2 致病性错义突变的结构分析及脱敏门控中新发的从头变异体的鉴定。

Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gate.

机构信息

Department of Haematology, University of Cambridge, NHS Blood and Transplant Centre, Cambridge, UK.

NIHR BioResource, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, UK.

出版信息

Mol Genet Genomic Med. 2020 Jul;8(7):e1106. doi: 10.1002/mgg3.1106. Epub 2020 Apr 29.

DOI:10.1002/mgg3.1106
PMID:32347641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7336760/
Abstract

BACKGROUND

Cys-loop receptors control neuronal excitability in the brain and their dysfunction results in numerous neurological disorders. Recently, six missense variants in GABRA2, a member of this family, have been associated with early infantile epileptic encephalopathy (EIEE). We identified a novel de novo missense variant in GABRA2 in a patient with EIEE and performed protein structural analysis of the seven variants.

METHODS

The novel variant was identified by trio whole-genome sequencing. We performed protein structural analysis of the seven variants, and compared them to previously reported pathogenic mutations at equivalent positions in other Cys-loop receptors. Additionally, we studied the distribution of disease-associated variants in the transmembrane helices of these proteins.

RESULTS

The seven variants are in the transmembrane domain, either close to the desensitization gate, the activation gate, or in inter-subunit interfaces. Six of them have pathogenic mutations at equivalent positions in other Cys-loop receptors, emphasizing the importance of these residues. Also, pathogenic mutations are more common in the pore-lining helix, consistent with this region being highly constrained for variation in control populations.

CONCLUSION

Our study reports a novel pathogenic variant in GABRA2, characterizes the regions where pathogenic mutations are in the transmembrane helices, and underscores the value of considering sequence, evolutionary, and structural information as a strategy for variant interpretation of novel missense mutations.

摘要

背景

Cys 环受体控制大脑中的神经元兴奋性,其功能障碍会导致多种神经疾病。最近,该家族的一个成员 GABRA2 中的六个错义变异与早发性婴儿癫痫性脑病 (EIEE) 有关。我们在一名 EIEE 患者中发现了 GABRA2 中的一个新的从头错义变异,并对这七个变异进行了蛋白质结构分析。

方法

通过三人体全基因组测序鉴定新的变异。我们对这七个变异进行了蛋白质结构分析,并将它们与其他 Cys 环受体中等效位置的先前报道的致病性突变进行了比较。此外,我们研究了这些蛋白质的跨膜螺旋中与疾病相关的变异的分布。

结果

这七个变异位于跨膜域,要么靠近脱敏门,要么靠近激活门,要么位于亚基界面。其中六个在其他 Cys 环受体中具有等效位置的致病性突变,这强调了这些残基的重要性。此外,在孔衬螺旋中更常见致病性突变,这与该区域在对照人群中变异高度受限一致。

结论

我们的研究报告了 GABRA2 中的一个新的致病性变异,描述了致病性突变位于跨膜螺旋的区域,并强调了将序列、进化和结构信息作为新型错义突变变异解释的策略的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/550b5c5cba01/MGG3-8-e1106-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/903fcaa3c4fd/MGG3-8-e1106-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/f411f6141b51/MGG3-8-e1106-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/6a369a672395/MGG3-8-e1106-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/550b5c5cba01/MGG3-8-e1106-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/903fcaa3c4fd/MGG3-8-e1106-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/f411f6141b51/MGG3-8-e1106-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/6a369a672395/MGG3-8-e1106-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f1/7336760/550b5c5cba01/MGG3-8-e1106-g004.jpg

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