Atp5if1-flox 基因敲除小鼠

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产品名称

Atp5if1-flox 基因敲除小鼠

产品编号

S-CKO-01364

品系全称

C57BL/6NCya-Atp5if1em1flox/Cya

品系背景

C57BL/6NCya

品系编号

CKOCMP-11983-Atp5if1-B6N-VA

品系状态

使用本品系发表的文献需注明: Atp5if1-flox 基因敲除小鼠 mice (Strain S-CKO-01364) were purchased from Cyagen.
交付类型
周龄
性别
基因型
数量
cKO小鼠库模型

基本信息

基因研究概述

质控标准

基因
基因全称
ATP synthase inhibitory factor subunit 1
基因别称
Atpi,Atpif1,IF(1),If1
染色体号
Chr 4 (Mouse)
转录本 ID
NCBI: XM_030253107 | Ensembl: ENSMUST00000067496
修饰方式
条件性基因敲除
靶向范围
Exon 3
敲除长度
~1.1 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:1196457Knockout mice exhibit normal growth and breeding but are protected from TAC-pressure overload and isoproterenol infusion-induced cardiac hypertrophy. A different KO reduces neutrophil levels and leads to resistance to DSS-induced colitis and increased susceptibility to diet-induced obesity.
ATP5IF1,也称为IF1(Inhibitor Factor 1),是一种重要的线粒体蛋白。它主要与线粒体ATP合酶(F1F0-ATPase)的γ亚基结合,抑制ATP合酶的ATP水解活性。ATP合酶是线粒体氧化磷酸化系统(OXPHOS)的关键组成部分,负责将ADP和无机磷酸盐合成ATP,为细胞提供能量。因此,ATP5IF1对线粒体能量代谢和细胞功能具有重要影响。

ATP5IF1在多种疾病中发挥重要作用。例如,在急性髓系白血病(AML)中,ATP5IF1的过表达与不良预后相关。研究发现,CEBPAbZIP-in患者中,ATP5IF1等线粒体复合物V基因的过表达与更差的生存率相关[1]。此外,在心脏衰竭中,ATP5IF1等线粒体复合物V基因的过表达与心脏重塑和功能受损相关[2]。在神经系统中,ATP5IF1在额叶和颞叶皮质中的表达存在差异,提示其可能参与神经代谢通路[3]。在男性不育症中,ATP5IF1的表达异常与Sertoli细胞功能障碍相关[4]。在癌症中,ATP5IF1的表达上调与肿瘤的发生发展相关。研究发现,ATP5IF1基因敲除可以抑制肿瘤的生长,并增强细胞对细胞凋亡的敏感性[5]。此外,ATP5IF1的表达上调与子宫体子宫内膜癌的预后不良相关[6]。在炎症性肠病中,ATP5IF1基因敲除可以减轻结肠炎的严重程度[7]。

综上所述,ATP5IF1是一种重要的线粒体蛋白,参与调节线粒体能量代谢和细胞功能。ATP5IF1在多种疾病中发挥重要作用,包括急性髓系白血病、心脏衰竭、神经系统疾病、男性不育症、癌症和炎症性肠病。ATP5IF1的研究有助于深入理解线粒体能量代谢的调控机制,为疾病的治疗和预防提供新的思路和策略。

参考文献:
1. Tien, Feng-Ming, Yao, Chi-Yuan, Tsai, Xavier Cheng-Hong, Hou, Hsin-An, Tien, Hwei-Fang. 2024. Dysregulated immune and metabolic pathways are associated with poor survival in adult acute myeloid leukemia with CEBPA bZIP in-frame mutations. In Blood cancer journal, 14, 15. doi:10.1038/s41408-023-00975-8. https://pubmed.ncbi.nlm.nih.gov/38253683/
2. Giménez-Escamilla, Isaac, Benedicto, Carlota, Pérez-Carrillo, Lorena, Tarazón, Estefanía, Roselló-Lletí, Esther. 2024. Alterations in Mitochondrial Oxidative Phosphorylation System: Relationship of Complex V and Cardiac Dysfunction in Human Heart Failure. In Antioxidants (Basel, Switzerland), 13, . doi:10.3390/antiox13030285. https://pubmed.ncbi.nlm.nih.gov/38539818/
3. Raabe, Janice, Wittig, Ilka, Laurette, Patrick, Eschenhagen, Thomas, Cuello, Friederike. 2024. Physioxia rewires mitochondrial complex composition to protect stem cell viability. In Redox biology, 77, 103352. doi:10.1016/j.redox.2024.103352. https://pubmed.ncbi.nlm.nih.gov/39341035/
4. Xu, Long, Sun, Haidan, Zhang, Yang, Wang, Bo, Liu, Weiming. 2021. Proteomic analysis of human frontal and temporal cortex using iTRAQ-based 2D LC-MS/MS. In Chinese neurosurgical journal, 7, 27. doi:10.1186/s41016-021-00241-5. https://pubmed.ncbi.nlm.nih.gov/33952343/
5. Wei, Lei, Feng, Zonggang, Dou, Qian, Zhao, Xinghua, Hao, Bin. . Dysregulation of MTFR2, ATP5IF1 and BAK1 in Sertoli cells relates to idiopathic non-obstructive azoospermia via inhibiting mitochondrial fission and inducing mitochondrial dysfunction†. In Biology of reproduction, 110, 408-418. doi:10.1093/biolre/ioad150. https://pubmed.ncbi.nlm.nih.gov/37903059/
6. Galber, Chiara, Fabbian, Simone, Gatto, Cristina, Bellanda, Massimo, Giorgio, Valentina. 2023. The mitochondrial inhibitor IF1 binds to the ATP synthase OSCP subunit and protects cancer cells from apoptosis. In Cell death & disease, 14, 54. doi:10.1038/s41419-023-05572-y. https://pubmed.ncbi.nlm.nih.gov/36690622/
7. Liu, Jinhui, Chen, Tian, Yang, Min, Bai, Jianling, Yu, Hao. 2021. Development of an Oxidative Phosphorylation-Related and Immune Microenvironment Prognostic Signature in Uterine Corpus Endometrial Carcinoma. In Frontiers in cell and developmental biology, 9, 753004. doi:10.3389/fcell.2021.753004. https://pubmed.ncbi.nlm.nih.gov/34901000/