Tert-flox Mouse
一般名
Tert-flox
製品ID
S-CKO-06159
背景情報
C57BL/6JCya
系統ID
CKOCMP-21752-Tert-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Tert-flox Mouse(カタログ番号S-CKO-06159)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
Tert-flox
系統ID
CKOCMP-21752-Tert-B6J-VA
遺伝子名
製品ID
S-CKO-06159
遺伝子別名
TR, TP2, TRT, EST2, TCS1
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 13
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
ENSMUST00000022104
NCBIトランスクリプトID
NM_009354
ターゲット領域
Exon 3~5
有効領域の大きさ
~2.9 kb
遺伝子研究の概要
Telomerase reverse transcriptase (TERT) is the catalytic subunit of telomerase. Telomerase, an RNA-dependent DNA polymerase, plays a crucial role in maintaining telomere length, which is essential for cells to overcome senescence induced by telomere shortening during DNA replication [5,7]. Telomerase activity is tightly regulated, and TERT expression is repressed in most differentiated cells but can be reactivated in cancer cells, contributing to tumorigenesis through telomere-dependent and-independent mechanisms [1,4,6].
TERT promoter mutations are highly recurrent in over 50 cancer types and are the most common mutation in many cancers [2]. These mutations upregulate TERT transcription, enabling tumor cells to achieve unlimited proliferative capacity by elongating telomeres [3]. In differentiated thyroid carcinoma, TERT-p mutations are associated with high-risk clinicopathological features and worse prognosis [3]. In CNS tumors like meningiomas, medulloblastomas, and primary glial neoplasms, TERT promoter mutations lead to up-regulation of TERT transcription, while in ependymomas and pediatric brain tumors, TERT promoter hypermethylation has the same effect [5]. In melanoma, TERT-p mutations are frequent in chronic and non-chronic sun-damage melanoma and correlate with adverse prognosis, and in acral melanoma, TERT copy number gains and gene amplification predict reduced survival [8]. In urothelial carcinomas, TERT promoter mutations and aberrant methylation play important roles in TERT transcription activation and telomerase activation, and have potential in non-invasive diagnostics, recurrence monitoring, and outcome prediction [9].
In conclusion, TERT is essential for telomere maintenance and its dysregulation, often through promoter mutations or epigenetic changes, is a key event in cancer development across multiple cancer types. The study of TERT in cancer, especially through the identification of its promoter mutations in various malignancies, provides insights into tumorigenesis mechanisms and potential biomarkers for diagnosis, prognosis, and therapeutic targets.
References:
1. Dratwa, Marta, Wysoczańska, Barbara, Łacina, Piotr, Kubik, Tomasz, Bogunia-Kubik, Katarzyna. 2020. TERT-Regulation and Roles in Cancer Formation. In Frontiers in immunology, 11, 589929. doi:10.3389/fimmu.2020.589929. https://pubmed.ncbi.nlm.nih.gov/33329574/
2. Bell, Robert J A, Rube, H Tomas, Xavier-Magalhães, Ana, Song, Jun S, Costello, Joseph F. 2016. Understanding TERT Promoter Mutations: A Common Path to Immortality. In Molecular cancer research : MCR, 14, 315-23. doi:10.1158/1541-7786.MCR-16-0003. https://pubmed.ncbi.nlm.nih.gov/26941407/
3. Matsuse, Michiko, Mitsutake, Norisato. 2023. TERT promoter mutations in thyroid cancer. In Endocrine journal, 70, 1035-1049. doi:10.1507/endocrj.EJ23-0136. https://pubmed.ncbi.nlm.nih.gov/37532521/
4. Liu, Mingdi, Zhang, Yuning, Jian, Yongping, Wang, Yishu, Xu, Zhi-Xiang. 2024. The regulations of telomerase reverse transcriptase (TERT) in cancer. In Cell death & disease, 15, 90. doi:10.1038/s41419-024-06454-7. https://pubmed.ncbi.nlm.nih.gov/38278800/
5. Patel, Bhuvic, Taiwo, Rukayat, Kim, Albert H, Dunn, Gavin P. 2020. TERT, a promoter of CNS malignancies. In Neuro-oncology advances, 2, vdaa025. doi:10.1093/noajnl/vdaa025. https://pubmed.ncbi.nlm.nih.gov/32226942/
6. Song, Young Shin, Park, Young Joo. 2020. Mechanisms of TERT Reactivation and Its Interaction with BRAFV600E. In Endocrinology and metabolism (Seoul, Korea), 35, 515-525. doi:10.3803/EnM.2020.304. https://pubmed.ncbi.nlm.nih.gov/32981294/
7. Heidenreich, Barbara, Kumar, Rajiv. 2016. TERT promoter mutations in telomere biology. In Mutation research. Reviews in mutation research, 771, 15-31. doi:10.1016/j.mrrev.2016.11.002. https://pubmed.ncbi.nlm.nih.gov/28342451/
8. Motaparthi, Kiran, Kim, Jinah, Andea, Aleodor A, Fung, Maxwell A, Emanuel, Patrick O. 2020. TERT and TERT promoter in melanocytic neoplasms: Current concepts in pathogenesis, diagnosis, and prognosis. In Journal of cutaneous pathology, 47, 710-719. doi:10.1111/cup.13691. https://pubmed.ncbi.nlm.nih.gov/32202662/
9. Liu, Tiantian, Li, Shihong, Xia, Chuanyou, Xu, Dawei. 2023. TERT promoter mutations and methylation for telomerase activation in urothelial carcinomas: New mechanistic insights and clinical significance. In Frontiers in immunology, 13, 1071390. doi:10.3389/fimmu.2022.1071390. https://pubmed.ncbi.nlm.nih.gov/36713366/
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。
