Rnf149-KO Mouse
一般名
Rnf149-KO
製品ID
S-KO-18754
背景情報
C57BL/6JCya
系統ID
KOCMP-67702-Rnf149-B6J-VB
状況
このマウス系統を論文で使用する場合は、「Rnf149-KO Mouse(カタログ番号S-KO-18754)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
Rnf149-KO
系統ID
KOCMP-67702-Rnf149-B6J-VB
遺伝子名
製品ID
S-KO-18754
遺伝子別名
Greul4, Gm15832, 1600023E10Rik
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conventional knockout
染色体
Chr 1
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
ENSMUST00000062525
NCBIトランスクリプトID
NM_001033135
ターゲット領域
Exon 2
有効領域の大きさ
~1.1 kb
遺伝子研究の概要
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/
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精子検査
凍結前の精子濃度を測定し、精子の生存能力の判定します。
凍結後の精子では、各バッチから1本の凍結保存された精子を選び出し、体外受精に使用します。
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