Tmem117-KO 基因敲除小鼠

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产品名称

Tmem117-KO 基因敲除小鼠

产品编号

S-KO-09336

品系全称

C57BL/6NCya-Tmem117em1/Cya

品系背景

C57BL/6NCya

品系编号

KOCMP-320709-Tmem117-B6N-VA

品系状态

使用本品系发表的文献需注明: Tmem117-KO 基因敲除小鼠 mice (Strain S-KO-09336) were purchased from Cyagen.
交付类型
周龄
性别
基因型
数量

基本信息

基因研究概述

质控标准

基因
基因全称
transmembrane protein 117
基因别称
B930062P21Rik
染色体号
Chr 15 (Mouse)
转录本 ID
NCBI: NM_178789 | Ensembl: ENSMUST00000080141
修饰方式
全身性基因敲除
靶向范围
Exon 3
敲除长度
~0.1 kb
品系说明
该品系是基于策略设计时的数据库信息制作而成,建议您在购买前查询最新的数据库和相关文献,以获取最准确的表型信息。
表型提示
MGI:2444580Mice with loss of expression in the posterior pituitary display loss of vassopressin neurons and transient increases in hypoglycemia induced glucagon secretion.
Tmem117,也称为Transmembrane protein 117,是一种位于内质网(ER)和细胞膜上的跨膜蛋白。Tmem117的基因表达受内质网应激(ER stress)的调控,在内质网应激条件下,Tmem117的表达水平会下降[1]。Tmem117在内质网应激介导的细胞死亡通路中发挥重要作用,其表达下调可以导致线粒体膜电位(ΔΨm)的丧失,增加活性氧水平,上调内质网应激传感器C/EBP同源蛋白的表达和活性caspase-3的表达,从而促进细胞凋亡[2]。此外,Tmem117的表达还与多种疾病相关,例如炎症性肠病[3]、流感A病毒(IAV)、麻疹、风疹和腮腺炎[4]等。Tmem117的表达水平还与动物的乳腺结构[5]、羊的产乳性状[6]和体重及体型性状[7]相关。此外,Tmem117还可以与多梳抑制复合物2(PRC2)结合,影响组蛋白修饰,进而调控基因表达和干细胞的多能性维持[8]。Tmem117的基因多态性与注意力缺陷多动障碍(ADHD)的药物反应相关[9]。

综上所述,Tmem117是一种重要的跨膜蛋白,参与调控内质网应激、细胞凋亡、基因表达和干细胞的多能性维持等生物学过程。Tmem117的表达与多种疾病相关,为疾病的治疗和预防提供了新的思路和策略。

参考文献:
1. Maruyama, Ryuto, Sugiyama, Tomoyasu. 2023. ER Stress Decreases Gene Expression Of Transmembrane Protein 117 Via Activation of PKR-like ER Kinase. In Cell biochemistry and biophysics, 81, 459-468. doi:10.1007/s12013-023-01150-3. https://pubmed.ncbi.nlm.nih.gov/37421592/
2. Tamaki, Tomoya, Kamatsuka, Kenta, Sato, Taku, Hattori, Masahiro, Sugiyama, Tomoyasu. 2017. A novel transmembrane protein defines the endoplasmic reticulum stress-induced cell death pathway. In Biochemical and biophysical research communications, 486, 149-155. doi:10.1016/j.bbrc.2017.03.017. https://pubmed.ncbi.nlm.nih.gov/28285135/
3. Maruyama, Ryuto, Kiyohara, Yuki, Kudo, Yasuhiro, Sugiyama, Tomoyasu. 2023. Effects of the anti-inflammatory drug celecoxib on cell death signaling in human colon cancer. In Naunyn-Schmiedeberg's archives of pharmacology, 396, 1171-1185. doi:10.1007/s00210-023-02399-4. https://pubmed.ncbi.nlm.nih.gov/36692829/
4. Zhu, Xiaobo, Zou, Yixin, Jia, Linna, Yang, Sheng, Huang, Peng. 2023. Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases. In Frontiers in genetics, 14, 1164274. doi:10.3389/fgene.2023.1164274. https://pubmed.ncbi.nlm.nih.gov/37020999/
5. Zhou, Wen, Zhang, Cheng-Long, Han, Zhipeng, Yang, Ruizhi, Liu, Shudong. 2024. Genome-wide selection reveals candidate genes associated with multiple teats in Hu sheep. In Animal biotechnology, 35, 2380766. doi:10.1080/10495398.2024.2380766. https://pubmed.ncbi.nlm.nih.gov/39034460/
6. Nazar, Mudasir, Abdalla, Ismail Mohamed, Chen, Zhi, Yang, Zhangping, Lu, Xubin. 2022. Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle. In Animals : an open access journal from MDPI, 12, . doi:10.3390/ani12192542. https://pubmed.ncbi.nlm.nih.gov/36230283/
7. Tao, L, He, X Y, Pan, L X, Gan, S Q, Chu, M X. 2020. Genome-wide association study of body weight and conformation traits in neonatal sheep. In Animal genetics, 51, 336-340. doi:10.1111/age.12904. https://pubmed.ncbi.nlm.nih.gov/31960458/
8. Liao, Meijian, Sun, Xiaolin, Gao, Shoucui, Zhang, Yaou. 2021. A Class of Protein-Coding RNAs Binds to Polycomb Repressive Complex 2 and Alters Histone Methylation. In Frontiers in oncology, 11, 739830. doi:10.3389/fonc.2021.739830. https://pubmed.ncbi.nlm.nih.gov/34804929/
9. Zhao, Yilu, Fu, Zhao, Barnett, Eric J, Faraone, Stephen V, Yang, Li. 2025. Genome data based deep learning identified new genes predicting pharmacological treatment response of attention deficit hyperactivity disorder. In Translational psychiatry, 15, 46. doi:10.1038/s41398-025-03250-5. https://pubmed.ncbi.nlm.nih.gov/39920114/