Scube3-flox Mouse
一般名
Scube3-flox
製品ID
S-CKO-19057
背景情報
C57BL/6JCya
系統ID
CKOCMP-268935-Scube3-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Scube3-flox Mouse(カタログ番号S-CKO-19057)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
Scube3-flox
系統ID
CKOCMP-268935-Scube3-B6J-VA
遺伝子名
製品ID
S-CKO-19057
遺伝子別名
CEGF3, D030038I21Rik
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 17
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
ENSMUST00000043503
NCBIトランスクリプトID
NM_001004366
ターゲット領域
Exon 2~3
有効領域の大きさ
~2.1 kb
遺伝子研究の概要
Scube3, or signal peptide-CUB-EGF domain-containing protein 3, is a multifunctional secreted glycoprotein. It functions as a co-receptor for various growth factors and is involved in multiple signaling pathways, such as TGF-β, BMP, and FGF signaling pathways [1-9]. It plays a crucial role in development, including hair follicle, tooth, bone, and muscle development, and is also implicated in various disease processes like cancer and autoimmune diseases [1-8]. Genetic models, especially mouse models, have been instrumental in studying its function.
In hair follicle development, Hedgehog signaling-induced upregulation of Scube3 in dermal papilla fibroblasts promotes hair growth, with Scube3 protein injection alone sufficient to trigger new hair growth [1]. In tooth development, epithelium-derived Scube3 translocates to the mesenchyme, promoting dental mesenchymal stem cell proliferation, migration, and odontoblastic differentiation [2]. In hepatocellular carcinoma, knockdown of Scube3 inhibits cell proliferation, promotes apoptosis, and arrests the cell cycle, suggesting its role in cancer progression [3]. In breast cancer, high Scube3 expression indicates poor prognosis [4]. In human bone marrow mesenchymal stem cells, Scube3 promotes osteogenic differentiation and mitophagy through the BMP2/TGF-β signaling pathway [5]. Loss-of-function variants in Scube3 in humans and Scube3-/-mice lead to a developmental disorder with craniofacial, dental, and skeletal defects due to impaired BMP-mediated chondrogenesis and osteogenesis [6]. In tongue squamous cell carcinoma, silencing Scube3 restrains cell proliferation, migration, and invasion [7]. In Chinese populations, variants in Scube3 are associated with systemic lupus erythematosus susceptibility, and its mRNA expression is lower in patients [8]. In zebrafish, knockdown of scube3 suppresses fast muscle development by inhibiting FGF signaling [9]. In non-small cell lung cancer, high Scube3 expression is correlated with lymph node involvement, advanced TNM stages, and poor prognosis [10].
In conclusion, Scube3 is essential for normal development and is involved in various disease processes. Gene knockout and conditional knockout mouse models, along with other functional studies, have significantly contributed to understanding its role in hair, tooth, bone, and muscle development, as well as in cancer and autoimmune diseases. These insights provide potential targets for therapeutic interventions in related diseases.
References:
1. Liu, Yingzi, Guerrero-Juarez, Christian F, Xiao, Fei, Li, Ji, Plikus, Maksim V. 2022. Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state. In Developmental cell, 57, 1758-1775.e7. doi:10.1016/j.devcel.2022.06.005. https://pubmed.ncbi.nlm.nih.gov/35777353/
2. Wang, Zijie, Chen, Chuying, Zhang, Jiayi, Wu, Jiayuan, Tian, Zhihui. 2023. Epithelium-derived SCUBE3 promotes polarized odontoblastic differentiation of dental mesenchymal stem cells and pulp regeneration. In Stem cell research & therapy, 14, 130. doi:10.1186/s13287-023-03353-0. https://pubmed.ncbi.nlm.nih.gov/37189178/
3. Xu, Pan, Luo, Aoran, Xiong, Chuan, Yan, Liang, Luo, Qiang. 2022. SCUBE3 downregulation modulates hepatocellular carcinoma by inhibiting CCNE1 via TGFβ/PI3K/AKT/GSK3β pathway. In Cancer cell international, 22, 1. doi:10.1186/s12935-021-02402-z. https://pubmed.ncbi.nlm.nih.gov/34980127/
4. Huo, Qin, He, Xi, Li, Zhenwei, Chen, Siqi, Xie, Ni. 2021. SCUBE3 serves as an independent poor prognostic factor in breast cancer. In Cancer cell international, 21, 268. doi:10.1186/s12935-021-01947-3. https://pubmed.ncbi.nlm.nih.gov/34006286/
5. Chen, Hongyu, Wu, Xiaoyong, Lan, Yinan, Zhang, Weijun, Xue, DeTing. . SCUBE3 promotes osteogenic differentiation and mitophagy in human bone marrow mesenchymal stem cells through the BMP2/TGF-β signaling pathway. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 38, e70011. doi:10.1096/fj.202400991R. https://pubmed.ncbi.nlm.nih.gov/39250278/
6. Lin, Yuh-Charn, Niceta, Marcello, Muto, Valentina, Yang, Ruey-Bing, Tartaglia, Marco. 2020. SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling. In American journal of human genetics, 108, 115-133. doi:10.1016/j.ajhg.2020.11.015. https://pubmed.ncbi.nlm.nih.gov/33308444/
7. Zhu, Minhui, Ma, Yi, Wang, Wei, Zheng, Hongliang, Zhang, Caiyun. . SCUBE3 Exerts a Tumor-Promoting Effect in Tongue Squamous Cell Carcinoma by Promoting CEBPA Binding to the CCL2 Promoter. In Molecular cancer research : MCR, 22, 482-494. doi:10.1158/1541-7786.MCR-23-0038. https://pubmed.ncbi.nlm.nih.gov/38349738/
8. Qi, Yuan-Yuan, Zhao, Ya-Fei, Zhai, Ya-Ling, Ning, Xiang-Hui, Zhao, Zhan-Zheng. 2020. SCUBE3 Is Likely a Susceptibility Gene for Systemic Lupus Erythematosus for Chinese Populations. In Journal of immunology research, 2020, 8897936. doi:10.1155/2020/8897936. https://pubmed.ncbi.nlm.nih.gov/33274247/
9. Tu, Cheng-Fen, Tsao, Ku-Chi, Lee, Shyh-Jye, Yang, Ruey-Bing. 2014. SCUBE3 (signal peptide-CUB-EGF domain-containing protein 3) modulates fibroblast growth factor signaling during fast muscle development. In The Journal of biological chemistry, 289, 18928-42. doi:10.1074/jbc.M114.551929. https://pubmed.ncbi.nlm.nih.gov/24849601/
10. Zhao, Chao, qin, Qin, Wang, Qianqian, Chen, Sunxiao, Deng, Anmei. . SCUBE3 overexpression predicts poor prognosis in non-small cell lung cancer. In Bioscience trends, 7, 264-9. doi:. https://pubmed.ncbi.nlm.nih.gov/24390364/
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