Rrbp1-flox Mouse
一般名
Rrbp1-flox
製品ID
S-CKO-17030
背景情報
C57BL/6JCya
系統ID
CKOCMP-81910-Rrbp1-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Rrbp1-flox Mouse(カタログ番号S-CKO-17030)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
Rrbp1-flox
系統ID
CKOCMP-81910-Rrbp1-B6J-VA
遺伝子名
製品ID
S-CKO-17030
遺伝子別名
p180, mRRp0, mRRp2, ES/130, mRRp10, mRRp41, mRRp47, mRRp1.8, mRRp15a, mRRp15b, mRRp5.4, mRRp16.8, mKIAA1398, 1700087N07Rik, 5730465C04Rik
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 2
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
ENSMUST00000016072
NCBIトランスクリプトID
NM_024281
ターゲット領域
Exon 2
有効領域の大きさ
~2.7 kb
遺伝子研究の概要
RRBP1, also known as ribosome-binding protein 1 or P180, is a ribosome-binding transmembrane protein of the endoplasmic reticulum. It is involved in multiple biological functions.
In normal physiological conditions, it contributes to processes such as local translation in axons, where it binds to mRNAs enriched for axonal membrane proteins and regulates local translation through its role in axonal ER-ribosome interactions [2]. It also plays a part in the regulation of mitophagy. When there is mitochondrial protein import stress (MPIS), RRBP1 relocates to the mitochondrial vicinity, and together with NLRX1, controls the recruitment and lipidation of LC3, a crucial step in mitophagy [1,8].
In disease-related studies, RRBP1 shows potential oncogenic properties. In upper tract urothelial carcinoma (UTUC), gene body hypomethylation of RRBP1 is associated with its high expression, which is related to carcinogenesis, metastasis, and chemoresistance [3]. In bladder cancer, high RRBP1 expression is associated with tumor stage, lymph node metastasis, and shorter overall survival time, and its knockdown inhibits cell migration and invasion [4]. In oral squamous cell carcinoma, RRBP1 up-regulation is related to cisplatin-resistance, and its inhibition restores cisplatin-mediated cell death [5]. In prostate cancer, METTL3 stabilizes RRBP1 mRNA in an m6A-dependent manner, and RRBP1 exerts an oncogenic role [7]. In epithelial ovarian cancer, high RRBP1 expression is related to FIGO stage, histological grade, histological type, and lymph node metastasis, and is an independent predictor of overall survival and disease-free survival [9]. In prostate cancer, RRBP1 expression is significantly higher compared to non-cancerous tissues and is associated with T stage, lymph node metastasis, PSA, and Gleason score, serving as an independent prognostic factor [10]. In bone metastatic cancer, depletion of RRBP1 enhances the osteoblastic phenotype expression, suggesting its role in the bone microenvironment [6].
In conclusion, RRBP1 has essential functions in normal biological processes like local translation and mitophagy. In disease, especially in multiple types of cancers, it is closely associated with tumor malignancy, metastasis, and chemoresistance. Studies on RRBP1, including those using gene-knockout or conditional-knockout models if applicable in the future, help to understand its role in these biological processes and diseases, potentially providing new targets for cancer treatment.
References:
1. Killackey, Samuel A, Bi, Yuntian, Soares, Fraser, Arnoult, Damien, Girardin, Stephen E. 2022. Mitochondrial protein import stress regulates the LC3 lipidation step of mitophagy through NLRX1 and RRBP1. In Molecular cell, 82, 2815-2831.e5. doi:10.1016/j.molcel.2022.06.004. https://pubmed.ncbi.nlm.nih.gov/35752171/
2. Koppers, Max, Özkan, Nazmiye, Nguyen, Ha H, Hoogenraad, Casper C, Farías, Ginny G. 2024. Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions. In Developmental cell, 59, 2053-2068.e9. doi:10.1016/j.devcel.2024.05.005. https://pubmed.ncbi.nlm.nih.gov/38815583/
3. Luo, Hao-Lun, Liu, Hui-Ying, Chang, Yin-Lun, Huang, Chun-Chieh, Peng, Jei-Ming. 2021. Hypomethylated RRBP1 Potentiates Tumor Malignancy and Chemoresistance in Upper Tract Urothelial Carcinoma. In International journal of molecular sciences, 22, . doi:10.3390/ijms22168761. https://pubmed.ncbi.nlm.nih.gov/34445467/
4. Wang, Mingshuai, Liu, Sai, Zhou, Bolin, Ping, Hao, Xing, Nianzeng. 2020. RRBP1 is highly expressed in bladder cancer and is associated with migration and invasion. In Oncology letters, 20, 203. doi:10.3892/ol.2020.12066. https://pubmed.ncbi.nlm.nih.gov/32963609/
5. Shriwas, Omprakash, Arya, Rakesh, Mohanty, Sibasish, Nanda, Ranjan K, Dash, Rupesh. 2021. RRBP1 rewires cisplatin resistance in oral squamous cell carcinoma by regulating Hippo pathway. In British journal of cancer, 124, 2004-2016. doi:10.1038/s41416-021-01336-7. https://pubmed.ncbi.nlm.nih.gov/33762722/
6. Chen, Rui, Wang, Yue, Xu, Yang, Xia, Chun, Zhang, Bing. 2022. RRBP1 depletion of bone metastatic cancer cells contributes to enhanced expression of the osteoblastic phenotype. In Frontiers in oncology, 12, 1005152. doi:10.3389/fonc.2022.1005152. https://pubmed.ncbi.nlm.nih.gov/36568157/
7. Feng, Yuqing, Li, Zenghui, Zhu, Jinwei, Shi, Junfeng, Zhang, Dingxiao. 2024. Stabilization of RRBP1 mRNA via an m6A-dependent manner in prostate cancer constitutes a therapeutic vulnerability amenable to small-peptide inhibition of METTL3. In Cellular and molecular life sciences : CMLS, 81, 414. doi:10.1007/s00018-024-05418-6. https://pubmed.ncbi.nlm.nih.gov/39367907/
8. Killackey, Samuel A, Bi, Yuntian, Philpott, Dana J, Arnoult, Damien, Girardin, Stephen E. 2022. Mitochondria-ER cooperation: NLRX1 detects mitochondrial protein import stress and promotes mitophagy through the ER protein RRBP1. In Autophagy, 19, 1601-1603. doi:10.1080/15548627.2022.2129763. https://pubmed.ncbi.nlm.nih.gov/36170592/
9. Ma, Jing, Ren, Sujing, Ding, Jing, Ma, Rong, Meng, Fanling. 2019. Expression of RRBP1 in epithelial ovarian cancer and its clinical significance. In Bioscience reports, 39, . doi:10.1042/BSR20190656. https://pubmed.ncbi.nlm.nih.gov/31285390/
10. Li, Tieqiu, Wang, Qianqian, Hong, Xiuqin, Li, Jiahui, Lei, Bin. 2019. RRBP1 is highly expressed in prostate cancer and correlates with prognosis. In Cancer management and research, 11, 3021-3027. doi:10.2147/CMAR.S186632. https://pubmed.ncbi.nlm.nih.gov/31118771/
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