Gria2-flox Mouse
Common Name
Gria2-flox
제품 ID
S-CKO-02746
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-14800-Gria2-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Gria2-flox Mouse (카탈로그 번호 S-CKO-02746)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
기본 정보
품종 계통
Gria2-flox
품종 계통계통 ID
CKOCMP-14800-Gria2-B6J-VA
유전자명
제품 ID
S-CKO-02746
유전자 별칭
GluA2, Glur2, GluR-B, Glur-2, gluR-K2
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 3
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000075316
NCBI 전사체 ID
NM_013540
타겟 영역
Exon 4
유효 영역 크기
~1.4 kb
유전자 연구 개요
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/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
Cyagen문의하기
맞춤형 동물 모델 관련 상담을 위해 Cyagen 전문가와 연락해 보세요. 아래 양식을 작성하여 상담을 시작하거나 견적을 요청하시기 바랍니다.
Cyagen은 고객님의 개인정보를 소중히 여깁니다. 최신 제품, 서비스 및 인사이트를 안내드리고자 합니다. 고객님의 수신 설정은 다음과 같습니다:
해당 커뮤니케이션은 언제든지 수신 거부하실 수 있습니다. 수신 거부 방법 및 데이터 보호에 대한 자세한 내용은 개인정보처리방침을 참고해 주시기 바랍니다.
아래 버튼을 클릭함으로써, 요청하신 콘텐츠 제공을 위해 본 양식을 통해 제출된 개인정보를 Cyagen이 저장 및 처리하는 데 동의하게 됩니다.
