Gpt2-flox Mouse
Common Name
Gpt2-flox
제품 ID
S-CKO-00685
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-108682-Gpt2-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Gpt2-flox Mouse (카탈로그 번호 S-CKO-00685)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
Gpt2-flox
품종 계통계통 ID
CKOCMP-108682-Gpt2-B6J-VA
유전자명
제품 ID
S-CKO-00685
유전자 별칭
ALT2, 4631422C05Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 8
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000034136
NCBI 전사체 ID
NM_173866
타겟 영역
Exon 4
유효 영역 크기
~1.8 kb
유전자 연구 개요
GPT2, also known as glutamate pyruvate transaminase 2, is a nuclear-encoded mitochondrial enzyme. It catalyzes the reversible transfer of an amino group from glutamate to pyruvate, generating alanine and alpha-ketoglutarate. This reaction is involved in glutamine catabolism and plays a role in replenishing tricarboxylic acid (TCA) cycle intermediates, thus being crucial for cellular metabolism [7].
In glioblastoma, hypoxia-inducible factor (HIF)-2 directly induces GPT2, promoting tumor growth. Genetic or pharmacological inhibition of GPT2 decreases cell growth and migration, and knockout of GPT2 in mice inhibits tumor growth [1]. In triple-negative breast cancer, GPT2 is up-regulated and promotes metastasis. Exosomal GPT2 derived from these cells activates BTRC to enhance metastasis, and GPT2 knockout reduces lung metastasis in mice [2]. In acute myeloid leukemia, IGF2BP2 regulates GPT2 in the glutamine metabolism pathways, and inhibiting IGF2BP2 shows anti-leukemia effects [3]. In the locus coeruleus, GPT2 deficiency in mice causes early neurodegeneration, with loss of tyrosine hydroxylase-positive neurons, abnormal action potentials, and microgliosis and astrogliosis [4]. In breast cancer, GPT2 promotes metastasis through the GABA-GABAA receptor-PKC-CREB signaling pathway, and GPT2 knockout reduces metastasis and prolongs survival in mice [5]. In triple-negative breast cancer, abrogating GPT2 decreases TCA cycle intermediates, impairs mTORC1 activity, and induces autophagy, resulting in decreased tumor growth in xenograft studies [6]. In lung adenocarcinoma, inhibition of GPT2 suppresses tumor growth and increases CD4 and CD8 expression, and shows enhanced antitumor immunity when combined with anti-PD-L1 [8].
In conclusion, GPT2 plays essential roles in various biological processes and disease conditions. Gene knockout mouse models have significantly contributed to understanding its role in cancer, neurodegeneration, and metabolic-related disorders, revealing its potential as a therapeutic target in these disease areas.
References:
1. Zhang, Bo, Chen, Yan, Bao, Lei, Luo, Weibo. 2022. GPT2 Is Induced by Hypoxia-Inducible Factor (HIF)-2 and Promotes Glioblastoma Growth. In Cells, 11, . doi:10.3390/cells11162597. https://pubmed.ncbi.nlm.nih.gov/36010673/
2. Cui, Mingqing, Peng, Jiawei, Zhou, Yuanyuan, Wang, Xixi, Cui, Daxiang. 2023. Exosomal GPT2 derived from triple-negative breast cancer cells promotes metastasis by activating BTRC. In Thoracic cancer, 14, 2018-2025. doi:10.1111/1759-7714.14984. https://pubmed.ncbi.nlm.nih.gov/37287397/
3. Weng, Hengyou, Huang, Feng, Yu, Zhaojin, Huang, Huilin, Chen, Jianjun. 2022. The m6A reader IGF2BP2 regulates glutamine metabolism and represents a therapeutic target in acute myeloid leukemia. In Cancer cell, 40, 1566-1582.e10. doi:10.1016/j.ccell.2022.10.004. https://pubmed.ncbi.nlm.nih.gov/36306790/
4. Baytas, Ozan, Kauer, Julie A, Morrow, Eric M. 2022. Loss of mitochondrial enzyme GPT2 causes early neurodegeneration in locus coeruleus. In Neurobiology of disease, 173, 105831. doi:10.1016/j.nbd.2022.105831. https://pubmed.ncbi.nlm.nih.gov/35908744/
5. Li, Na, Xu, Xiang, Liu, Dan, Li, Qun, Mi, Jun. 2023. The delta subunit of the GABAA receptor is necessary for the GPT2-promoted breast cancer metastasis. In Theranostics, 13, 1355-1369. doi:10.7150/thno.80544. https://pubmed.ncbi.nlm.nih.gov/36923530/
6. Mitra, Devina, Vega-Rubin-de-Celis, Silvia, Royla, Nadine, Müller-Decker, Karin, Wiemann, Stefan. 2021. Abrogating GPT2 in triple-negative breast cancer inhibits tumor growth and promotes autophagy. In International journal of cancer, 148, 1993-2009. doi:10.1002/ijc.33456. https://pubmed.ncbi.nlm.nih.gov/33368291/
7. Ouyang, Qing, Kavanaugh, Brian C, Joesch-Cohen, Lena, Liu, Judy S, Morrow, Eric M. 2019. GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. In Human genetics, 138, 1183-1200. doi:10.1007/s00439-019-02057-x. https://pubmed.ncbi.nlm.nih.gov/31471722/
8. Wang, Bolin, Pei, Jinli, Xu, Shengnan, Liu, Jie, Yu, Jinming. 2023. System analysis based on glutamine catabolic-related enzymes identifies GPT2 as a novel immunotherapy target for lung adenocarcinoma. In Computers in biology and medicine, 165, 107415. doi:10.1016/j.compbiomed.2023.107415. https://pubmed.ncbi.nlm.nih.gov/37657356/
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:
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