Gnai3-KO Mouse
Common Name
Gnai3-KO
제품 ID
S-KO-19469
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-14679-Gnai3-B6J-VC
상태
이 마우스 계통을 논문에서 사용할 경우, “Gnai3-KO Mouse (카탈로그 번호 S-KO-19469)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
Gnai3-KO
품종 계통계통 ID
KOCMP-14679-Gnai3-B6J-VC
유전자명
제품 ID
S-KO-19469
유전자 별칭
Hg1a, Gnai-3, Galphai3
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 3
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000000001
NCBI 전사체 ID
NM_010306
타겟 영역
Exon 2~3
유효 영역 크기
~1.9 kb
유전자 연구 개요
Gnai3, also known as Guanine nucleotide binding protein, alpha inhibiting activity polypeptide 3, is involved in multiple biological processes. It participates in signaling pathways, such as those related to cytokine regulation and G-protein-coupled receptor signaling, and is of great biological importance in processes like cell migration, inflammation, and tumorigenesis [4,2,1]. Genetic models, like Gnai3-iresGFP reporter mice, are useful tools for studying its expression patterns [3].
In mice, GNAI1 and GNAI3 double-knockout (DKO) mice showed more severe colitis and significantly more colonic tumors compared to control mice after treatment with dextran sulfate sodium (DSS) and azoxymethane (AOM). The increased tumor development was associated with activation of NF-κB and STAT3, increased levels of GNAI2, nitric oxide synthase 2, and IL6, and changes in immune cell populations. Blocking IL6 with an antibody reduced the expansion of myeloid-derived suppressor cells (MDSCs) and the number of tumors in DKO mice, indicating that GNAI3 suppresses DSS-plus-AOM-induced colon tumor development by blocking IL6 signaling and down-regulating GNAI2 expression [1]. In hepatocellular carcinoma (HCC) cells, GNAI3 inhibits cell migration and invasion, and its down-regulation, potentially caused by up-regulation of miR-222, promotes HCC cell migration and invasion [4]. In non-alcoholic fatty liver disease (NAFLD) models, GNAI3 knockout enhanced dysregulated hepatic lipid metabolism and liver damage in mice, and down-regulation of GNAI3 promoted cellular lipid accumulation in HepG2 cells, suggesting GNAI3 is involved in NAFLD development [5].
In conclusion, Gnai3 plays crucial roles in various biological processes and disease conditions. The use of gene knockout mouse models, such as in colitis-associated tumorigenesis and NAFLD studies, has revealed its functions in inhibiting tumor development and regulating lipid metabolism. Its down-regulation in certain cancers like HCC is associated with increased cell migration and invasion. Understanding Gnai3's functions provides insights into disease mechanisms and potential therapeutic targets.
References:
1. Li, Zhi-Wei, Sun, Beicheng, Gong, Ting, Zhou, Xiqiao, Chu, Wen-Ming. 2019. GNAI1 and GNAI3 Reduce Colitis-Associated Tumorigenesis in Mice by Blocking IL6 Signaling and Down-regulating Expression of GNAI2. In Gastroenterology, 156, 2297-2312. doi:10.1053/j.gastro.2019.02.040. https://pubmed.ncbi.nlm.nih.gov/30836096/
2. Guo, Ling, Sun, Hua, Pu, Jiao. 2024. GNAI3 mediated by Lin28A regulates lipopolysaccharide-induced inflammation and osteogenic differentiation in periodontal stem cells by mediating the NF-κB/NLRP3 inflammasome pathway. In Archives of oral biology, 163, 105974. doi:10.1016/j.archoralbio.2024.105974. https://pubmed.ncbi.nlm.nih.gov/38636252/
3. Leiss, Veronika, Reisinger, Ellen, Speidel, Annika, Beer-Hammer, Sandra, Nürnberg, Bernd. 2021. Analyses of Gnai3-iresGFP reporter mice reveal unknown Gαi3 expression sites. In Scientific reports, 11, 14271. doi:10.1038/s41598-021-93591-0. https://pubmed.ncbi.nlm.nih.gov/34253772/
4. Zhang, Yu, Yao, Jian, Huan, Lin, Liang, Linhui, He, Xianghuo. 2014. GNAI3 inhibits tumor cell migration and invasion and is post-transcriptionally regulated by miR-222 in hepatocellular carcinoma. In Cancer letters, 356, 978-84. doi:10.1016/j.canlet.2014.11.013. https://pubmed.ncbi.nlm.nih.gov/25444921/
5. Zhu, Hanzhang, Ge, Ke, Lu, Jun, Jia, Changku. . Downregulation of GNAI3 Promotes the Pathogenesis of Methionine/Choline-Deficient Diet-Induced Nonalcoholic Fatty Liver Disease. In Gut and liver, 14, 492-499. doi:10.5009/gnl19115. https://pubmed.ncbi.nlm.nih.gov/31694365/
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
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