Prkdc-KO Mouse
一般名
Prkdc-KO
製品ID
S-KO-03780
背景情報
C57BL/6NCya
系統ID
KOCMP-19090-Prkdc-B6N-VA
状況
このマウス系統を論文で使用する場合は、「Prkdc-KO Mouse(カタログ番号S-KO-03780)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
Prkdc-KO
系統ID
KOCMP-19090-Prkdc-B6N-VA
遺伝子名
製品ID
S-KO-03780
遺伝子別名
p460, scid, slip, DNAPK, DNPK1, HYRC1, XRCC7, dxnph, DOXNPH, DNAPDcs, DNA-PKcs
遺伝子別名
C57BL/6NCya
NCBI ID
修正
Conventional knockout
染色体
Chr 16
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
ENSMUST00000023352
NCBIトランスクリプトID
NM_011159
ターゲット領域
Exon 2~10
有効領域の大きさ
~7.7 kb
遺伝子研究の概要
Prkdc, also known as Protein Kinase, DNA-Activated, Catalytic Polypeptide, encodes the DNA-dependent protein kinase catalytic subunit (DNA-PKcs). DNA-PKcs plays a major role in nonhomologous end-joining DNA repair, which is crucial for maintaining genomic stability. It has been implicated in various biological processes and is associated with pathways like cell cycle regulation. Genetic models, such as KO/CKO mouse models, are valuable for studying its functions [3].
In osteosarcoma, loss-of-function experiments showed that the loss of Prkdc significantly increased sensitivity to doxorubicin, as Prkdc recruited GDE2 to stabilize GNAS and activate AKT, conferring chemoresistance [1]. In gastric cancer, hsa_circ_0136666 upregulated Prkdc expression by sponging miR-375-3p, promoting tumor progression and immune escape [2]. In skin wound healing, knockdown of circ_PRKDC promoted keratinocyte migration through the miR-31/FBN1 axis [4]. In pan-cancer analysis, high Prkdc expression was associated with a worse prognosis, while its mutations might lead to better survival [5]. In ovarian cancer, PRKDC-mediated non-homologous end-joining may play a crucial role in chromosome 8 aneuploidy-driven progression [6]. In liver hepatocellular carcinoma, targeting Prkdc activated antitumor immunity and sensitized to chemotherapy and targeted therapy [7]. In renal transplantation, up-regulation of Prkdc in the donor kidney was associated with poor renal dysfunction after transplantation [8].
In conclusion, Prkdc is essential for DNA repair and has far-reaching impacts on multiple biological processes. Studies using KO/CKO mouse models and other loss-of-function experiments have revealed its roles in various disease conditions, including cancer and post-transplantation renal dysfunction. Understanding Prkdc functions provides potential therapeutic targets for these diseases.
References:
1. Zhang, Wenchao, Li, Wei, Yin, Chi, Tu, Chao, Li, Zhihong. . PRKDC Induces Chemoresistance in Osteosarcoma by Recruiting GDE2 to Stabilize GNAS and Activate AKT. In Cancer research, 84, 2873-2887. doi:10.1158/0008-5472.CAN-24-0163. https://pubmed.ncbi.nlm.nih.gov/38900943/
2. Miao, Zhenyan, Li, Jifei, Wang, Yu, Zheng, Lufeng, Xing, Yingying. 2023. Hsa_circ_0136666 stimulates gastric cancer progression and tumor immune escape by regulating the miR-375/PRKDC Axis and PD-L1 phosphorylation. In Molecular cancer, 22, 205. doi:10.1186/s12943-023-01883-y. https://pubmed.ncbi.nlm.nih.gov/38093288/
3. Yin, Yuting, He, Qinglian, Li, Yuling, Li, Ziqi, Zhu, Wei. 2020. Emerging functions of PRKDC in the initiation and progression of cancer. In Tumori, 107, 483-488. doi:10.1177/0300891620950472. https://pubmed.ncbi.nlm.nih.gov/32867618/
4. Han, Dawei, Liu, Wenhui, Li, Guangshuai, Liu, Linbo. 2021. Circ_PRKDC knockdown promotes skin wound healing by enhancing keratinocyte migration via miR-31/FBN1 axis. In Journal of molecular histology, 52, 681-691. doi:10.1007/s10735-021-09996-8. https://pubmed.ncbi.nlm.nih.gov/34143322/
5. Yang, Xiawei, Yang, Feng, Lan, Liugen, Li, Haibin, Sun, Xuyong. 2022. Potential value of PRKDC as a therapeutic target and prognostic biomarker in pan-cancer. In Medicine, 101, e29628. doi:10.1097/MD.0000000000029628. https://pubmed.ncbi.nlm.nih.gov/35801800/
6. Luan, Wenqing, Cheng, Hongyan, Xie, Haoling, Li, Yi, Chang, Xiaohong. 2024. PRKDC-Mediated NHEJ May Play a Crucial Role in Aneuploidy of Chromosome 8-Driven Progression of Ovarian Cancer. In International journal of molecular sciences, 25, . doi:10.3390/ijms25094825. https://pubmed.ncbi.nlm.nih.gov/38732044/
7. Pan, Yitong, Zhu, Qiyao, Hong, Ting, Cheng, Jun, Tang, Xinhui. 2024. Targeting PRKDC activates the efficacy of antitumor immunity while sensitizing to chemotherapy and targeted therapy in liver hepatocellular carcinoma. In Aging, 16, 9047-9071. doi:10.18632/aging.205855. https://pubmed.ncbi.nlm.nih.gov/38787389/
8. Cao, Zhijun, Jiang, Hao, Zhao, Chunchun, Jiang, Minjun, Wang, Zhenfan. 2023. Up-regulation of PRKDC was associated with poor renal dysfunction after renal transplantation: A multi-centre analysis. In Journal of cellular and molecular medicine, 27, 1362-1372. doi:10.1111/jcmm.17737. https://pubmed.ncbi.nlm.nih.gov/37002788/
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。
