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C57BL/6JCya-Dusp2em1flox/Cya
Common Name:
Dusp2-flox
Product ID:
S-CKO-02114
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
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Basic Information
Strain Name
Dusp2-flox
Strain ID
CKOCMP-13537-Dusp2-B6J-VA
Gene Name
Dusp2
Product ID
S-CKO-02114
Gene Alias
PAC1
Background
C57BL/6JCya
NCBI ID
13537
Modification
Conditional knockout
Chromosome
2
Phenotype
MGI:101911
Document
Click here to download >>
Application
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More
Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Dusp2em1flox/Cya mice (Catalog S-CKO-02114) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000028846
NCBI RefSeq
NM_010090
Target Region
Exon 1~4
Size of Effective Region
~2.2 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Dusp2, a member of the mitogen-activated protein kinase phosphatase family, is involved in abolishing the activation of mitogen-activated protein kinases (MAPKs) [8]. It plays critical roles in immune processes, inflammatory responses, and cancer progression [8]. Associated pathways include the AKT1, MEK/ERK, P38 MAPK, and STAT3 pathways among others [1,2,3].

In pancreatic cancer, DUSP2 promotes apoptosis through recruiting CSNK2A1 to inhibit AKT1 phosphorylation under hypoxic conditions, and activation of AKT1 leads to DUSP2 degradation via the AKT1/TRIM21 loop [1]. In bladder cancer, its down-regulation is associated with poor prognosis, and overexpression inhibits cell proliferation, metastasis, and affects the immune microenvironment by regulating MEK/ERK and P38 MAPK through PTPN7 [2,8]. In lupus nephritis, DUSP2 reduces proteinuria, cytokine levels, and improves renal tissue injury by inhibiting STAT3 phosphorylation [3]. In zebrafish, DUSP2 deletion promotes Mauthner cell axonal regeneration at an early stage, possibly by enhancing JNK phosphorylation [4]. In acute kidney injury, DUSP2-STAT1 axis regulates renal tubular epithelial cell pyroptosis, with DUSP2 deletion promoting pyroptosis and DUSP2 overexpression ameliorating AKI [5]. In gastric cancer, exosomal miR-519a-3p activates the MAPK/ERK pathway by targeting DUSP2, causing M2-like macrophage polarization and promoting liver metastasis [6]. In high-glucose-induced vascular endothelial cell dysfunction, interfering with Dusp2 promotes cell functions and alleviates mouse diabetic hindlimb ischemia by promoting p38 MAPK pathway activation [7].

In conclusion, Dusp2 is a key regulator in multiple biological processes and diseases. Gene-knockout models, such as in zebrafish and mice, have been instrumental in revealing its functions in cancer, kidney diseases, and axonal regeneration. Understanding Dusp2's role provides potential therapeutic targets for various diseases, including pancreatic, bladder, and gastric cancers, as well as lupus nephritis and acute kidney injury.

References:
1. Zhang, Yangyang, Kong, Rui, Yang, Wenbo, Hu, Jisheng, Sun, Bei. 2023. DUSP2 recruits CSNK2A1 to suppress AKT1-mediated apoptosis resistance under hypoxic microenvironment in pancreatic cancer. In Cancer letters, 568, 216288. doi:10.1016/j.canlet.2023.216288. https://pubmed.ncbi.nlm.nih.gov/37390887/
2. Zou, Fan, Rao, Ting, Chen, Wu, Yu, Weimin, Cheng, Fan. 2023. DUSP2 affects bladder cancer prognosis by down-regulating MEK/ERK and P38 MAPK signaling pathways through PTPN7. In Cellular signalling, 112, 110893. doi:10.1016/j.cellsig.2023.110893. https://pubmed.ncbi.nlm.nih.gov/37739277/
3. Liu, Xingzhong, Chen, Jie, Liu, Lu. 2023. DUSP2 inhibits the progression of lupus nephritis in mice by regulating the STAT3 pathway. In Open life sciences, 18, 20220649. doi:10.1515/biol-2022-0649. https://pubmed.ncbi.nlm.nih.gov/37483429/
4. Shao, Guo-Jian, Wang, Xin-Liang, Wei, Mei-Li, Ren, Da-Long, Hu, Bing. . DUSP2 deletion with Nuclease technology promotes Mauthner cell axonal regeneration at the early stage of zebrafish. In Neural regeneration research, 18, 577-581. doi:10.4103/1673-5374.350208. https://pubmed.ncbi.nlm.nih.gov/36018180/
5. Xiong, Jiachuan, Ran, Li, Zhu, Yingguo, Zhao, Jinghong, Yang, Ke. 2022. DUSP2-mediated inhibition of tubular epithelial cell pyroptosis confers nephroprotection in acute kidney injury. In Theranostics, 12, 5069-5085. doi:10.7150/thno.72291. https://pubmed.ncbi.nlm.nih.gov/35836796/
6. Qiu, Shengkui, Xie, Li, Lu, Chen, Li, Bowen, Xu, Zekuan. 2022. Gastric cancer-derived exosomal miR-519a-3p promotes liver metastasis by inducing intrahepatic M2-like macrophage-mediated angiogenesis. In Journal of experimental & clinical cancer research : CR, 41, 296. doi:10.1186/s13046-022-02499-8. https://pubmed.ncbi.nlm.nih.gov/36217165/
7. Jiang, Xinmiao, Yan, Qiong, He, Jiaqi, Nie, Jungang, Kang, Ting. 2023. Interfering with Dusp2 alleviates high glucose-induced vascular endothelial cell dysfunction by promoting p38 MAPK pathway activation. In Experimental cell research, 430, 113720. doi:10.1016/j.yexcr.2023.113720. https://pubmed.ncbi.nlm.nih.gov/37479052/
8. Yin, Hubin, He, Weiyang, Li, Yunhai, Lin, Yong, Gou, Xin. 2018. Loss of DUSP2 predicts a poor prognosis in patients with bladder cancer. In Human pathology, 85, 152-161. doi:10.1016/j.humpath.2018.11.007. https://pubmed.ncbi.nlm.nih.gov/30458195/
Quality Control Standard
Sperm Test

Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.

Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.

Environmental Standards:SPF
Available Region:Global
Source:Cyagen
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