Usp13-KO Mouse
一般名
Usp13-KO
製品ID
S-KO-13988
背景情報
C57BL/6NCya
系統ID
KOCMP-72607-Usp13-B6N-VA
状況
このマウス系統を論文で使用する場合は、「Usp13-KO Mouse(カタログ番号S-KO-13988)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
Usp13-KO
系統ID
KOCMP-72607-Usp13-B6N-VA
遺伝子名
製品ID
S-KO-13988
遺伝子別名
ISOT3, IsoT-3, 2700071E21Rik
遺伝子別名
C57BL/6NCya
NCBI ID
修正
Conventional knockout
染色体
Chr 3
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
ENSMUST00000072312
NCBIトランスクリプトID
NM_001013024
ターゲット領域
Exon 4~5
有効領域の大きさ
~7.4 kb
遺伝子研究の概要
USP13, an ubiquitin-specific protease, is a deubiquitination (DUB) enzyme. It removes ubiquitin from substrates, preventing their proteasomal degradation. USP13 is involved in numerous cellular processes such as mitochondrial energy metabolism, autophagy, DNA damage response, and endoplasmic reticulum-associated degradation (ERAD) by regulating the deubiquitination of key substrate proteins [1,4]. Dysregulation of USP13 is associated with many diseases, especially malignant tumors [1]. Genetic models, like KO/CKO mouse models, can be valuable for studying its functions.
In a KPU mouse model (KrasG12D/+; Trp53flox/flox background with USP13 overexpression), USP13 was found to drive lung squamous cell carcinoma (LUSC) by altering lineage-determining factors in club cells and reinforcing their fate towards squamous carcinoma development [3]. In ccRCC, depletion of USP13 led to decreased cell proliferation in 2D and 3D assays and reduced tumor growth in vivo, as it promotes the deubiquitination and stability of ZHX2, a protein involved in ccRCC tumorigenesis [2]. In KRAS-mutant NSCLC, USP13 promoted metastasis, and its depletion could potentially be a treatment strategy as 2-methoxyestradiol, an inhibitor of USP13, suppressed metastasis in vitro and in vivo [5]. In GIST cells, inhibition of USP13 in murine xenograft models led to ATG5 decay and enhanced the treatment efficacy of imatinib [6]. In gastric cancer, depletion of USP13 in nude mouse experiments suppressed tumor growth in vivo, as USP13 deubiquitinates and stabilizes cyclin D1 to promote cell cycle progression and proliferation [7]. In lung adenocarcinoma with KRAS mutation, USP13 depletion promoted an autophagy-to-ferroptosis switch in vitro and in xenograft tumor mouse models [8]. In aged Usp13-deficient mice, there was impaired autophagic activity and increased vulnerability to bleomycin-induced fibrosis [9].
In conclusion, USP13 plays essential roles in various biological processes, especially in autophagy, cell cycle regulation, and lineage-determining factor regulation. Model-based research, particularly using KO/CKO mouse models, has revealed its significant contributions to diseases such as lung cancer, kidney cancer, NSCLC, GIST, gastric cancer, and idiopathic pulmonary fibrosis, suggesting that USP13 could be a potential therapeutic target for these diseases.
References:
1. Li, Xiaolong, Yang, Ge, Zhang, Wenyao, Zhao, Qi, Wang, Feng. 2022. USP13: Multiple Functions and Target Inhibition. In Frontiers in cell and developmental biology, 10, 875124. doi:10.3389/fcell.2022.875124. https://pubmed.ncbi.nlm.nih.gov/35445009/
2. Xie, Haibiao, Zhou, Jin, Liu, Xijuan, Gong, Kan, Zhang, Qing. 2022. USP13 promotes deubiquitination of ZHX2 and tumorigenesis in kidney cancer. In Proceedings of the National Academy of Sciences of the United States of America, 119, e2119854119. doi:10.1073/pnas.2119854119. https://pubmed.ncbi.nlm.nih.gov/36037364/
3. Kwon, Juntae, Zhang, Jinmin, Mok, Boram, Toretsky, Jeffrey, Han, Cecil. 2023. USP13 drives lung squamous cell carcinoma by switching lung club cell lineage plasticity. In Molecular cancer, 22, 204. doi:10.1186/s12943-023-01892-x. https://pubmed.ncbi.nlm.nih.gov/38093367/
4. Wang, Qian, Sun, Zhenzhen, Xia, Weiwei, Zhang, Yue, Jia, Zhanjun. 2022. Role of USP13 in physiology and diseases. In Frontiers in molecular biosciences, 9, 977122. doi:10.3389/fmolb.2022.977122. https://pubmed.ncbi.nlm.nih.gov/36188217/
5. Guo, Yanguan, Tian, Jiaxin, Guo, Yongjian, Hua, Zichun, Chen, Guo. 2023. Oncogenic KRAS effector USP13 promotes metastasis in non-small cell lung cancer through deubiquitinating β-catenin. In Cell reports, 42, 113511. doi:10.1016/j.celrep.2023.113511. https://pubmed.ncbi.nlm.nih.gov/38043062/
6. Gao, Zhishuang, Li, Chao, Sun, Haoyu, Li, Xueming, Xu, Hao. 2022. N6-methyladenosine-modified USP13 induces pro-survival autophagy and imatinib resistance via regulating the stabilization of autophagy-related protein 5 in gastrointestinal stromal tumors. In Cell death and differentiation, 30, 544-559. doi:10.1038/s41418-022-01107-8. https://pubmed.ncbi.nlm.nih.gov/36528756/
7. Ma, Cunying, Wang, Dandan, Tian, Zhuangfei, Jia, Jihui, Liu, Zhifang. 2023. USP13 deubiquitinates and stabilizes cyclin D1 to promote gastric cancer cell cycle progression and cell proliferation. In Oncogene, 42, 2249-2262. doi:10.1038/s41388-023-02739-x. https://pubmed.ncbi.nlm.nih.gov/37311811/
8. Chen, Ling, Ning, Jieling, Linghu, Li, Zhang, Bin, Tao, Yongguang. 2024. USP13 facilitates a ferroptosis-to-autophagy switch by activation of the NFE2L2/NRF2-SQSTM1/p62-KEAP1 axis dependent on the KRAS signaling pathway. In Autophagy, 21, 565-582. doi:10.1080/15548627.2024.2410619. https://pubmed.ncbi.nlm.nih.gov/39360581/
9. Liu, Yuan, Li, Zhen, Xiao, Huijuan, Dai, Huaping, Wang, Chen. . USP13 Deficiency Impairs Autophagy and Facilitates Age-related Lung Fibrosis. In American journal of respiratory cell and molecular biology, 68, 49-61. doi:10.1165/rcmb.2022-0002OC. https://pubmed.ncbi.nlm.nih.gov/36150040/
品質管理基準
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。
環境基準:
SPF対応地域:
グローバル由来:
Cyagenお問い合わせ
カスタムの動物モデルに関するご相談は、下記のフォームにご記入いただき、ご連絡いただくか見積もりをご依頼ください。
Cyagenはお客様のプライバシーを大変重視しています。当社の最新の製品や情報をお届けしたいと思っています。お客様の設定をご確認ください。
これらの配信はいつでも解除できます。配信停止方法およびデータ保護の詳細は プライバシーポリシー をご確認ください。
以下のボタンをクリックすることで、このフォームにご入力いただいた個人情報をCyagenが保存・処理し、ご要望のコンテンツを提供することに同意されたことになります。
