Gria2-flox Mouse
一般名
Gria2-flox
製品ID
S-CKO-02746
背景情報
C57BL/6JCya
系統ID
CKOCMP-14800-Gria2-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Gria2-flox Mouse(カタログ番号S-CKO-02746)はサイアジェンから購入しました。」と引用してください。
製品タイプ
年齢
遺伝子型
性別
数量
標準的な配送方法では、少なくとも3匹のヘテロ接合体キャリアを保証しています。ホモ接合体キャリアや指定された性別の個体の繁殖サービスも利用可能です。
基本情報
系統名
Gria2-flox
系統ID
CKOCMP-14800-Gria2-B6J-VA
遺伝子名
製品ID
S-CKO-02746
遺伝子別名
GluA2, Glur2, GluR-B, Glur-2, gluR-K2
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 3
表現型
アプリケーション
--
さらに
系統詳細
EnsemblトランスクリプトID
ENSMUST00000075316
NCBIトランスクリプトID
NM_013540
ターゲット領域
Exon 4
有効領域の大きさ
~1.4 kb
遺伝子研究の概要
Gria2, also known as Glutamate receptor, ionotropic, AMPA2 (alpha 2), encodes the GluA2 subunit of the AMPA receptor. AMPA receptors are tetrameric ligand-gated channels, and GluA2 is crucial as post-transcriptional editing at the Q607 site renders heteromultimeric AMPARs Ca2+-impermeable. This gene is involved in glutamatergic synaptic transmission, which is vital for normal brain function [2].
In lower extremity artery restenosis after percutaneous transluminal angioplasty (PTA), GRIA2 is highly differentially expressed in restenotic arterial plaques. Overexpression of GRIA2 promotes the proliferation and migration of vascular smooth muscle cells (VSMCs) through upregulation of ENPP3, suggesting its role in restenosis development [1].
In neurodevelopmental disorders, de-novo heterozygous mutations in GRIA2 have been found in patients with intellectual disability, autism spectrum disorder, Rett syndrome-like features, and seizures. Functional expression studies show that these mutations decrease agonist-evoked current mediated by mutant subunits [2]. A novel gain-of-function GRIA2 variant has been associated with neurodevelopmental delay and seizures, and the antiseizure drug perampanel was effective in treating the patient [7]. Also, in a patient with atypical autism spectrum disorder, a de novo GRIA2 variant was reported, expanding the phenotypic variation spectrum [3].
In methamphetamine-use disorder, serum GRIA2 is higher in patients, and miR-181a negatively regulates GRIA2 expression [5].
In Dazu Black Goats, SNPs in GRIA2 are associated with reproductive traits [6]. GRIA2 is also a useful diagnostic marker for solitary fibrous tumour [4].
In conclusion, Gria2 plays essential roles in multiple biological processes and disease conditions. Its functions in the nervous system related to synaptic transmission and in non-neural tissues such as in vascular smooth muscle cell regulation in restenosis, as well as its associations with various disorders like neurodevelopmental disorders, autism spectrum disorder, methamphetamine-use disorder, and reproductive traits in goats, are significant. Research on Gria2 using genetic models could potentially provide more insights into these disease mechanisms and lead to better treatment strategies.
References:
1. Zhou, Mi, Qi, Lixing, Gu, Yongquan. 2021. GRIA2/ENPP3 Regulates the Proliferation and Migration of Vascular Smooth Muscle Cells in the Restenosis Process Post-PTA in Lower Extremity Arteries. In Frontiers in physiology, 12, 712400. doi:10.3389/fphys.2021.712400. https://pubmed.ncbi.nlm.nih.gov/34504438/
2. Salpietro, Vincenzo, Dixon, Christine L, Guo, Hui, Kullmann, Dimitri M, Houlden, Henry. 2019. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. In Nature communications, 10, 3094. doi:10.1038/s41467-019-10910-w. https://pubmed.ncbi.nlm.nih.gov/31300657/
3. Cai, Qianyun, Zhou, Zhongjie, Luo, Rong, Yang, Fan, Yang, Zuozhen. 2022. Novel GRIA2 variant in a patient with atypical autism spectrum disorder and psychiatric symptoms: a case report. In BMC pediatrics, 22, 629. doi:10.1186/s12887-022-03702-7. https://pubmed.ncbi.nlm.nih.gov/36329391/
4. Vivero, Marina, Doyle, Leona A, Fletcher, Christopher D M, Mertens, Fredrik, Hornick, Jason L. 2014. GRIA2 is a novel diagnostic marker for solitary fibrous tumour identified through gene expression profiling. In Histopathology, 65, 71-80. doi:10.1111/his.12377. https://pubmed.ncbi.nlm.nih.gov/24456377/
5. Zhang, Kai, Wang, Qingzhong, Jing, Xuxiu, Yu, Shunying, Zhao, Min. 2016. miR-181a is a negative regulator of GRIA2 in methamphetamine-use disorder. In Scientific reports, 6, 35691. doi:10.1038/srep35691. https://pubmed.ncbi.nlm.nih.gov/27767084/
6. Fang, Xingqiang, Yang, Songjian, Chen, Meixi, Peng, Peng, Zhao, Yongju. 2023. Association analysis of polymorphisms at GLRB, GRIA2, and GASK1B genes with reproductive traits in Dazu Black Goats. In Animal biotechnology, 34, 4721-4729. doi:10.1080/10495398.2023.2187406. https://pubmed.ncbi.nlm.nih.gov/36927330/
7. Coombs, Ian D, Ziobro, Julie, Krotov, Volodymyr, Cull-Candy, Stuart G, Farrant, Mark. 2022. A gain-of-function GRIA2 variant associated with neurodevelopmental delay and seizures: Functional characterization and targeted treatment. In Epilepsia, 63, e156-e163. doi:10.1111/epi.17419. https://pubmed.ncbi.nlm.nih.gov/36161652/
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