H6pd-KO Mouse
一般名
H6pd-KO
製品ID
S-KO-18352
背景情報
C57BL/6JCya
系統ID
KOCMP-100198-H6pd-B6J-VB
状況
このマウス系統を論文で使用する場合は、「H6pd-KO Mouse(カタログ番号S-KO-18352)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
H6pd-KO
系統ID
KOCMP-100198-H6pd-B6J-VB
遺伝子名
製品ID
S-KO-18352
遺伝子別名
Gpd1, G6pd1, Gpd-1
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conventional 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
ENSMUST00000030830
NCBIトランスクリプトID
NM_173371
ターゲット領域
Exon 3
有効領域の大きさ
~1.4 kb
遺伝子研究の概要
H6pd, also known as hexose-6-phosphate dehydrogenase, is a microsomal enzyme that catalyzes the first two reactions of the oxidative chain of the pentose phosphate pathway [3]. This pathway is crucial for generating NADPH, which is involved in various cellular processes such as antioxidant defense, lipid biosynthesis, and steroid hormone metabolism. H6pd is located in the lumen of the endoplasmic reticulum and is particularly important in the context of corticosteroid metabolism, as it provides the NADPH required for the oxo-reductase activity of 11β-hydroxysteroid dehydrogenase type 1 (11-HSD1) [2].
Mice carrying a targeted mutation in H6pd have drastically decreased 11-HSD1 oxo-reductase activity, but increased 11-dehydrogenase activity [2]. These mice exhibit many phenotypic features similar to those with a mutation of 11-HSD1 itself, highlighting the significance of H6pd in corticosteroid metabolism. In addition, in cultured human amnion fibroblasts, small interfering RNA-mediated knockdown of H6PD expression significantly attenuated the conversion of cortisone to cortisol, further demonstrating its role in this metabolic process [5].
In terms of disease associations, in a case-control study of Iranian Kurdish women, variants of H6PD R453Q were found to affect the risk of polycystic ovary syndrome (PCOS), with statistically significant lower frequencies of certain genotypes and alleles in PCOS patients compared to controls [3]. Also, in gallbladder cancer, miR-551b-3p was shown to target and inhibit H6PD expression, and overexpression of miR-551b-3p suppressed epithelial-mesenchymal transition, migration, and invasion of cancer cells by inhibiting H6PD [1]. In retinoblastoma, long noncoding RNA TUG1 promoted cancer progression by sponging miR-516b-5p to upregulate H6PD expression [4].
In conclusion, H6pd plays an essential role in the pentose phosphate pathway, especially in providing NADPH for corticosteroid metabolism. The study of H6pd knockout mouse models has revealed its significance in this metabolic process. Additionally, research on H6pd has shown its potential associations with diseases such as PCOS, gallbladder cancer, and retinoblastoma, contributing to a better understanding of the disease mechanisms and potentially paving the way for new therapeutic strategies.
References:
1. Ji, Tao, Gao, Lijun, Yu, Zongbu. 2020. Tumor-suppressive microRNA-551b-3p targets H6PD to inhibit gallbladder cancer progression. In Cancer gene therapy, 28, 693-705. doi:10.1038/s41417-020-00252-x. https://pubmed.ncbi.nlm.nih.gov/33250514/
2. White, Perrin C, Rogoff, Daniela, McMillan, D Randy, Lavery, Gareth G. 2007. Hexose 6-phosphate dehydrogenase (H6PD) and corticosteroid metabolism. In Molecular and cellular endocrinology, 265-266, 89-92. doi:. https://pubmed.ncbi.nlm.nih.gov/17240046/
3. Naseri, Rozita, Alimoradi, Yosra, Sohrabi, Maryam, Abdolmaleki, Amir, Jalili, Cyrus. 2022. H6PD Gene Polymorphisms (R453Q and D151A) and Polycystic Ovary Syndrome: A Case-Control Study in A Population of Iranian Kurdish Women. In International journal of fertility & sterility, 16, 180-183. doi:10.22074/ijfs.2021.141690.1050. https://pubmed.ncbi.nlm.nih.gov/36029054/
4. Xiu, Caimei, Song, Ruiying, Jiang, Jing. . TUG1 promotes retinoblastoma progression by sponging miR-516b-5p to upregulate H6PD expression. In Translational cancer research, 10, 738-747. doi:10.21037/tcr-19-1480. https://pubmed.ncbi.nlm.nih.gov/35116405/
5. Wang, Weihua, Guo, Chunming, Li, Wenjiao, Myatt, Leslie, Sun, Kang. 2012. Involvement of GR and p300 in the induction of H6PD by cortisol in human amnion fibroblasts. In Endocrinology, 153, 5993-6002. doi:10.1210/en.2012-1531. https://pubmed.ncbi.nlm.nih.gov/23125313/
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