Dnaja1-flox Mouse
一般名
Dnaja1-flox
製品ID
S-CKO-02989
背景情報
C57BL/6JCya
系統ID
CKOCMP-15502-Dnaja1-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Dnaja1-flox Mouse(カタログ番号S-CKO-02989)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
Dnaja1-flox
系統ID
CKOCMP-15502-Dnaja1-B6J-VA
遺伝子名
製品ID
S-CKO-02989
遺伝子別名
Hsj2, HSJ-2, Nedd7
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 4
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
ENSMUST00000164233
NCBIトランスクリプトID
NM_001164671
ターゲット領域
Exon 4~6
有効領域の大きさ
~5.0 kb
遺伝子研究の概要
DNAJA1, also known as HDJ2, is a member of J-domain containing proteins or heat shock protein 40. It is involved in multiple cellular processes such as protein folding and degradation regulation. It interacts with other proteins and is associated with pathways related to cancer metastasis, metabolism, and spermatogenesis, playing an important role in various biological functions and disease-related processes. Genetic models, like knockout mice, are valuable for studying its functions [1-10].
In knockout mouse models, DNAJA1 knockout leads to complete infertility in male mice, as it is essential for spermatogenesis. DNAJA1 knockout also reduces protein polyubiquitination in the testis [3]. In human umbilical vein endothelial cells, DNAJA1-knockout alleviates heat stroke-induced endothelial barrier disruption by improving thermal tolerance and suppressing the MLCK-MLC signaling pathway [6]. In cancer-related studies, knockdown of DNAJA1 in head and neck squamous cell carcinoma (HNSCC) cell lines carrying unfolded mutant p53 (mutp53) decreases mutp53 levels, filopodia/lamellipodia formation, migratory potential, and active forms of CDC42/RAC1, and inhibits primary tumor growth and metastases to the lymph nodes and lungs. This indicates its role in promoting HNSCC metastasis in a mutp53-dependent manner [1]. In breast cancer, knockdown of DNAJA1 decreases cell proliferation, invasion, and metastasis both in vitro and in vivo, as it promotes these processes via the P53-R175H/NF-κB pathway [4]. In liver cancer, depletion of DNAJA1 in certain cell lines shows opposite effects on cell proliferation, invasion, and angiogenesis compared to overexpression, and in vivo it inhibits tumor growth and pulmonary metastasis [5]. In pancreatic ductal adenocarcinoma, DNAJA1 overexpression leads to mitochondrial fusion, an increase in Bcl-2 expression, and an anti-apoptotic phenotype [2].
In conclusion, DNAJA1 is essential for spermatogenesis and plays significant roles in various cancer-related processes such as metastasis and proliferation. Studies using knockout models have revealed its functions in these specific biological processes and disease conditions, highlighting its potential as a therapeutic target in cancer and its importance in male fertility research.
References:
1. Kaida, Atsushi, Yamamoto, Satomi, Parrales, Alejandro, Diaz, Francisco J, Iwakuma, Tomoo. 2021. DNAJA1 promotes cancer metastasis through interaction with mutant p53. In Oncogene, 40, 5013-5025. doi:10.1038/s41388-021-01921-3. https://pubmed.ncbi.nlm.nih.gov/34183772/
2. Roth, Heidi E, Bhinderwala, Fatema, Franco, Rodrigo, Zhou, You, Powers, Robert. 2021. DNAJA1 Dysregulates Metabolism Promoting an Antiapoptotic Phenotype in Pancreatic Ductal Adenocarcinoma. In Journal of proteome research, 20, 3925-3939. doi:10.1021/acs.jproteome.1c00233. https://pubmed.ncbi.nlm.nih.gov/34264680/
3. Mao, Jing-Jing, Dai, Xiao-Yu, Liu, Yun-Zi, Zhu, Jiang-Bo, Chen, Ji-Kuai. 2024. DNAJA1 regulates protein ubiquitination and is essential for spermatogenesis in the testes of mice and rats. In Reproductive toxicology (Elmsford, N.Y.), 130, 108701. doi:10.1016/j.reprotox.2024.108701. https://pubmed.ncbi.nlm.nih.gov/39208916/
4. Wu, Jiao, Yang, Qiao, Zhu, Ye, Wang, Jianmei, Ren, Xiaoli. 2023. DNAJA1 promotes proliferation and metastasis of breast cancer by activating mutant P53/NF-κB pathway. In Pathology, research and practice, 252, 154921. doi:10.1016/j.prp.2023.154921. https://pubmed.ncbi.nlm.nih.gov/37977037/
5. Yi, Lizhi, He, Shunhui, Cheng, Zhengyu, Ren, Xiaoli, Bai, Yang. 2022. DNAJA1 Stabilizes EF1A1 to Promote Cell Proliferation and Metastasis of Liver Cancer Mediated by miR-205-5p. In Journal of oncology, 2022, 2292481. doi:10.1155/2022/2292481. https://pubmed.ncbi.nlm.nih.gov/35586205/
6. Li, Lei, Wang, Ya-Wei, Chang, Xin, Chen, Ji-Kuai, Xu, Shuo-Gui. 2024. DNAJA1‑knockout alleviates heat stroke‑induced endothelial barrier disruption via improving thermal tolerance and suppressing the MLCK‑MLC signaling pathway. In Molecular medicine reports, 29, . doi:10.3892/mmr.2024.13211. https://pubmed.ncbi.nlm.nih.gov/38551163/
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