Rnf149-KO Mouse
Common Name
Rnf149-KO
제품 ID
S-KO-18754
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-67702-Rnf149-B6J-VB
상태
이 마우스 계통을 논문에서 사용할 경우, “Rnf149-KO Mouse (카탈로그 번호 S-KO-18754)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
Rnf149-KO
품종 계통계통 ID
KOCMP-67702-Rnf149-B6J-VB
유전자명
제품 ID
S-KO-18754
유전자 별칭
Greul4, Gm15832, 1600023E10Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 1
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000062525
NCBI 전사체 ID
NM_001033135
타겟 영역
Exon 2
유효 영역 크기
~1.1 kb
유전자 연구 개요
Rnf149, or ring finger protein 149, is an E3 ubiquitin ligase. It plays a crucial role in multiple biological processes by mediating ubiquitination-a process that can lead to protein degradation or altered protein function. It is involved in pathways related to inflammation, immune response, and cell proliferation. Understanding its function is important as it impacts various disease-related processes, and genetic models such as gene knockout (KO) mouse models are valuable tools for its study [1-6].
In macrophage-related processes, knockout of Rnf149 in murine models of myocardial infarction (MI) exacerbated cardiac dysfunction. It increased infiltration of pro-inflammatory monocytes/macrophages and impaired infarct healing. Rnf149 restricts inflammation by promoting ubiquitylation-dependent proteasomal degradation of IFNGR1 (interferon gamma receptor 1) in infiltrated macrophages [1]. In lipopolysaccharide/Toll-like receptor 4 (LPS/TLR4) signal transduction, Rnf149 negatively regulates the process by mediating ubiquitination-induced CD63 degradation [2]. In hepatocellular carcinoma (HCC), overexpression of Rnf149 significantly promoted cell proliferation, migration, and invasion, and it was upregulated in tumor tissues. It stimulated HCC progression via its E3 ubiquitin ligase activity and DNAJC25 was identified as its new substrate [3]. In esophageal squamous cell carcinoma (ESCC), Rnf149 was upregulated and high expression was associated with poor prognosis. It conferred cisplatin resistance by destabilizing PHLPP2 and activating the PI3K/AKT signalling pathway [4]. In acute myeloid leukaemia (AML), RNF149 accelerates AML progression, modifies the immune milieu, triggers CD8+T cell dysfunction, and influences drug resistance [5]. In antiviral immune responses, RNF149 modulates the type I IFN innate antiviral immune responses by degrading IRF3 [6].
In conclusion, Rnf149, as an E3 ubiquitin ligase, has a wide-reaching impact on various biological functions including immune response, inflammation, and cell proliferation. KO mouse models have been instrumental in revealing its role in diseases such as myocardial infarction, different types of cancers, and in immune-related processes. These findings suggest that Rnf149 could potentially be a therapeutic target for these disease conditions.
References:
1. Huang, Chun-Kai, Chen, Zhiyong, Zhou, Zhongxing, Yan, Xiaoxiang, Chai, Dajun. 2024. RNF149 Destabilizes IFNGR1 in Macrophages to Favor Postinfarction Cardiac Repair. In Circulation research, 135, 518-536. doi:10.1161/CIRCRESAHA.123.324023. https://pubmed.ncbi.nlm.nih.gov/38989590/
2. Yang, Xiu-An, Wang, Yingying, Gong, Mingyu, Zhang, Xiaoyu, Li, Yan. 2024. RNF149 negatively regulates LPS/TLR4 signal transduction by ubiquitination-mediated CD63 degradation. In Heliyon, 10, e34350. doi:10.1016/j.heliyon.2024.e34350. https://pubmed.ncbi.nlm.nih.gov/39104473/
3. Guo, Zhaoyu, Jiang, Pei, Dong, Qian, Tian, Chunyan, Sun, Aihua. 2023. RNF149 Promotes HCC Progression through Its E3 Ubiquitin Ligase Activity. In Cancers, 15, . doi:10.3390/cancers15215203. https://pubmed.ncbi.nlm.nih.gov/37958377/
4. Zhu, Jinrong, Tang, Jiuren, Wu, Yongqi, Jin, Xin, Zhang, Rongxin. 2023. RNF149 confers cisplatin resistance in esophageal squamous cell carcinoma via destabilization of PHLPP2 and activating PI3K/AKT signalling. In Medical oncology (Northwood, London, England), 40, 290. doi:10.1007/s12032-023-02137-z. https://pubmed.ncbi.nlm.nih.gov/37658961/
5. Wu, Xin, Wu, Zhongguang, Deng, Woding, Sun, Xiaoying, Zhao, Qiangqiang. 2023. Spatiotemporal evolution of AML immune microenvironment remodeling and RNF149-driven drug resistance through single-cell multidimensional analysis. In Journal of translational medicine, 21, 760. doi:10.1186/s12967-023-04579-5. https://pubmed.ncbi.nlm.nih.gov/37891580/
6. Wu, Mengyun, Cai, Jiamin, Qiao, Guodong, Yang, Yi, Zhang, Jinping. 2025. RNF149 modulates the type I IFN innate antiviral immune responses through degrading IRF3. In PLoS pathogens, 21, e1013051. doi:10.1371/journal.ppat.1013051. https://pubmed.ncbi.nlm.nih.gov/40245000/
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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