Gfra1-flox Mouse
一般名
Gfra1-flox
製品ID
S-CKO-02615
背景情報
C57BL/6JCya
系統ID
CKOCMP-14585-Gfra1-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Gfra1-flox Mouse(カタログ番号S-CKO-02615)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
Gfra1-flox
系統ID
CKOCMP-14585-Gfra1-B6J-VA
遺伝子名
製品ID
S-CKO-02615
遺伝子別名
GFRalpha-1
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 19
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
ENSMUST00000026076
NCBIトランスクリプトID
NM_010279
ターゲット領域
Exon 6
有効領域の大きさ
~2.1 kb
遺伝子研究の概要
Gfra1, the glycosylphosphatidylinositol-linked GDNF (glial cell derived neurotrophic factor) receptor alpha, is a coreceptor recognizing GDNF family ligands. It plays a crucial role in the development and maintenance of the nervous system, regulating proliferation, differentiation, and migration of neuronal cells. It is also involved in the RET/GFRA1 signaling which is important for ureteric bud morphogenesis [1,5].
In GFRa1 hypomorphic mice with 70%-80% reduction in GFRa1 expression, it leads to Hirschsprung's disease and associated enterocolitis, mirroring the disease progression in children [4]. In mice, inactivation of Ash2l in the ureteric bud lineage down-regulates Gfra1 expression, causing CAKUT-like phenotypes [5]. In mouse spermatogonial stem cells, Gfra1 silencing results in their differentiation via RET tyrosine kinase inactivation [9]. In osteosarcoma cells, cisplatin treatment induces GFRA1 expression, which promotes autophagy through the SRC-AMPK signaling axis, leading to chemoresistance, and GFRA1-induced autophagy promotes tumor growth in mouse xenograft models [1,3]. In glioblastoma, the GDNF/GFRA1 signaling pathway contributes to chemo-and radioresistance, as shown by CRISPR/Cas9 knock-outs of GDNF and GFRA1 in patient-derived models [2]. In gastric cancer, tumor-associated macrophage-derived GDNF promotes liver metastasis via a GFRA1-modulated autophagy flux [7]. Biallelic loss-of-function variants of GFRA1 in humans cause lethal bilateral renal agenesis [6,8].
In conclusion, Gfra1 is essential for the development of the nervous system, spermatogenesis, and the renal system. Mouse models, especially those with Gfra1 inactivation or reduced expression, have revealed its roles in various diseases. These include Hirschsprung's disease, enterocolitis, congenital anomalies of the kidney and urinary tract, osteosarcoma chemoresistance, glioblastoma chemo-and radioresistance, gastric cancer liver metastasis, and bilateral renal agenesis. Understanding Gfra1's functions through these models provides insights into disease mechanisms and potential therapeutic targets.
References:
1. Kim, Mihwa, Kim, Dae Joon. 2018. GFRA1: A Novel Molecular Target for the Prevention of Osteosarcoma Chemoresistance. In International journal of molecular sciences, 19, . doi:10.3390/ijms19041078. https://pubmed.ncbi.nlm.nih.gov/29617307/
2. Avenel, Inès C N, Ewald, Jesper D, Ariey-Bonnet, Jérémy, Michaelsen, Signe R, Kristensen, Bjarne W. 2024. GDNF/GFRA1 signaling contributes to chemo- and radioresistance in glioblastoma. In Scientific reports, 14, 17639. doi:10.1038/s41598-024-68626-x. https://pubmed.ncbi.nlm.nih.gov/39085346/
3. Kim, Mihwa, Jung, Ji-Yeon, Choi, Seungho, Kim, Won Jae, Kim, Dae Joon. 2016. GFRA1 promotes cisplatin-induced chemoresistance in osteosarcoma by inducing autophagy. In Autophagy, 13, 149-168. doi:10.1080/15548627.2016.1239676. https://pubmed.ncbi.nlm.nih.gov/27754745/
4. Porokuokka, L Lauriina, Virtanen, Heikki T, Lindén, Jere, Saarma, Mart, Andressoo, Jaan-Olle. 2018. Gfra1 Underexpression Causes Hirschsprung's Disease and Associated Enterocolitis in Mice. In Cellular and molecular gastroenterology and hepatology, 7, 655-678. doi:10.1016/j.jcmgh.2018.12.007. https://pubmed.ncbi.nlm.nih.gov/30594740/
5. Zhao, Ziyi, Dai, Xuantong, Jiang, Gengru, Lin, Fujun. 2023. ASH2L Controls Ureteric Bud Morphogenesis through the Regulation of RET/GFRA1 Signaling Activity in a Mouse Model. In Journal of the American Society of Nephrology : JASN, 34, 988-1002. doi:10.1681/ASN.0000000000000099. https://pubmed.ncbi.nlm.nih.gov/36758123/
6. Al-Shamsi, Bushra, Al-Kasbi, Ghalia, Al-Kindi, Adila, Al-Kharusi, Khalsa, Al-Maawali, Almundher. 2021. Biallelic loss-of-function variants of GFRA1 cause lethal bilateral renal agenesis. In European journal of medical genetics, 65, 104376. doi:10.1016/j.ejmg.2021.104376. https://pubmed.ncbi.nlm.nih.gov/34737117/
7. Ni, Bo, He, Xuan, Zhang, Yeqian, Chen, Huimin, Zhang, Zizhen. 2023. Tumor-associated macrophage-derived GDNF promotes gastric cancer liver metastasis via a GFRA1-modulated autophagy flux. In Cellular oncology (Dordrecht, Netherlands), 46, 315-330. doi:10.1007/s13402-022-00751-z. https://pubmed.ncbi.nlm.nih.gov/36808605/
8. Arora, Veronica, Khan, Suliman, El-Hattab, Ayman W, Bauer, Peter, Verma, Ishwar C. 2020. Biallelic Pathogenic GFRA1 Variants Cause Autosomal Recessive Bilateral Renal Agenesis. In Journal of the American Society of Nephrology : JASN, 32, 223-228. doi:10.1681/ASN.2020040478. https://pubmed.ncbi.nlm.nih.gov/33020172/
9. He, Zuping, Jiang, Jiji, Hofmann, Marie-Claude, Dym, Martin. 2007. Gfra1 silencing in mouse spermatogonial stem cells results in their differentiation via the inactivation of RET tyrosine kinase. In Biology of reproduction, 77, 723-33. doi:. https://pubmed.ncbi.nlm.nih.gov/17625109/
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。
