C57BL/6JCya-Stt3aem1/Cya
Common Name:
Stt3a-KO
Product ID:
S-KO-02715
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
Contact for Pricing
Basic Information
Strain Name
Stt3a-KO
Strain ID
KOCMP-16430-Stt3a-B6J-VA
Gene Name
Product ID
S-KO-02715
Gene Alias
B5; Itm1
Background
C57BL/6JCya
NCBI ID
Modification
Conventional knockout
Chromosome
9
Phenotype
Document
Application
--
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Stt3aem1/Cya mice (Catalog S-KO-02715) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000120381
NCBI RefSeq
NM_008408
Target Region
Exon 3
Size of Effective Region
~1.1 kb
Detailed Document
Overview of Gene Research
Stt3a, a key catalytic subunit of oligosaccharyltransferase (OST), is crucial for N-glycosylation, a process that modifies proteins by adding oligosaccharides. N-glycosylation is essential for protein stability, function, and various biological processes. It is involved in pathways like protein folding in the endoplasmic reticulum. Genetic models, such as knockout mouse models, are valuable for studying Stt3a's functions [2,4,5].
Knockout or inhibition of Stt3a in lung adenocarcinoma cell lines and mouse xenograft models suppressed cell proliferation, migration, invasion, and arrested the cell cycle, suggesting it promotes lung adenocarcinoma progression via the MAPK and PI3K/AKT signaling pathways [2]. In herpes simplex virus 1 (HSV-1) studies, cells lacking STT3B-OST activity and thus dependent on STT3A-OST for N-glycosylation, when treated with NGI-1 (an inhibitor of STT3A-OST), resulted in HSV-1 having cell type-dependent dysfunction [3]. In hepatocellular carcinoma, GMPS-mediated STT3A-dependent PD-L1 glycosylation modification drives tumor immune evasion, and targeting GMPS can suppress PD-L1 expression and tumor growth [1].
In conclusion, Stt3a-mediated N-glycosylation is essential for various biological processes and has implications in multiple diseases. Model-based research, especially KO/CKO mouse models, has revealed its role in promoting tumor progression in lung adenocarcinoma, affecting viral function in HSV-1, and contributing to tumor immune evasion in hepatocellular carcinoma, providing potential therapeutic targets for these diseases.
References:
1. Guo, Xinyu, Cui, Tianming, Sun, Linmao, Liu, Yao, Liu, Lianxin. 2024. A STT3A-dependent PD-L1 glycosylation modification mediated by GMPS drives tumor immune evasion in hepatocellular carcinoma. In Cell death and differentiation, , . doi:10.1038/s41418-024-01432-0. https://pubmed.ncbi.nlm.nih.gov/39690246/
2. Cheng, Jiahan, Xia, Liang, Hao, Xiaohu, Deng, Senyi, Liu, Lunxu. . Targeting STT3A produces an anti-tumor effect in lung adenocarcinoma by blocking the MAPK and PI3K/AKT signaling pathway. In Translational lung cancer research, 11, 1089-1107. doi:10.21037/tlcr-22-396. https://pubmed.ncbi.nlm.nih.gov/35832442/
3. Lu, Hua, Cherepanova, Natalia A, Gilmore, Reid, Contessa, Joseph N, Lehrman, Mark A. 2019. Targeting STT3A-oligosaccharyltransferase with NGI-1 causes herpes simplex virus 1 dysfunction. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 33, 6801-6812. doi:10.1096/fj.201802044RR. https://pubmed.ncbi.nlm.nih.gov/30811219/
4. Lu, Hua, Fermaintt, Charles S, Cherepanova, Natalia A, Yan, Nan, Lehrman, Mark A. 2018. Mammalian STT3A/B oligosaccharyltransferases segregate N-glycosylation at the translocon from lipid-linked oligosaccharide hydrolysis. In Proceedings of the National Academy of Sciences of the United States of America, 115, 9557-9562. doi:10.1073/pnas.1806034115. https://pubmed.ncbi.nlm.nih.gov/30181269/
5. Chang, Irene J, Byers, Heather M, Ng, Bobby G, Zhang, Bin, Lam, Christina. 2019. Factor VIII and vWF deficiency in STT3A-CDG. In Journal of inherited metabolic disease, 42, 325-332. doi:10.1002/jimd.12021. https://pubmed.ncbi.nlm.nih.gov/30701557/
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