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C57BL/6NCya-Bcat2em1flox/Cya
Common Name:
Bcat2-flox
Product ID:
S-CKO-01394
Background:
C57BL/6NCya
Product Type
Age
Genotype
Sex
Quantity
Price:
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Basic Information
Strain Name
Bcat2-flox
Strain ID
CKOCMP-12036-Bcat2-B6N-VA
Gene Name
Bcat2
Product ID
S-CKO-01394
Gene Alias
Bcat(m); Bcat-2; Eca40
Background
C57BL/6NCya
NCBI ID
12036
Modification
Conditional knockout
Chromosome
7
Phenotype
MGI:1276534
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/6NCya-Bcat2em1flox/Cya mice (Catalog S-CKO-01394) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000033098
NCBI RefSeq
NM_009737
Target Region
Exon 4~6
Size of Effective Region
~1.2 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Bcat2, or Branched-chain amino acid transaminase 2, is a key enzyme in the branched-chain amino acid (BCAA) catabolism pathway. It reversibly catalyzes the initial step of BCAA degradation to branched-chain acyl-CoA, playing a crucial role in maintaining BCAA homeostasis [3]. This metabolic pathway is associated with various biological processes and disease conditions, making Bcat2 an important gene for functional studies, and genetic models like KO/CKO mouse models are valuable tools for exploring its functions.

In pancreatic ductal adenocarcinoma (PDAC), pancreatic tissue-specific knockout of Bcat2 in LSL-KrasG12D/+; Pdx1-Cre (KC) mice impedes the progression of pancreatic intraepithelial neoplasia (PanIN). BCAT2 enhances BCAA uptake to sustain BCAA catabolism and mitochondrial respiration, and its inhibitor ameliorates PanIN formation in KC mice. Also, a lower-BCAA diet impedes PDAC development in mouse models [1].

In melanoma, BCAT2 deficiency leads to impaired tumor cell proliferation, invasion, and migration in vitro, and tumor growth and metastasis in vivo, as it promotes melanoma progression by epigenetically regulating fatty acid synthase (FASN) and ATP-citrate lyase (ACLY) expressions [2].

In colorectal cancer, BCAT2 deficiency promotes tumorigenesis through inhibition of BCAAs metabolism and chronic activation of mTORC1 [6].

In obese with psoriasis mice, the down-regulation of Bcat2 is related to the inhibition of the BCAA catabolism pathway and the aggravation of inflammation [4].

In white adipose tissue (WAT), adipose tissue knockout of Bcat2 in mice increases inguinal WAT browning and thermogenesis, making them resistant to high-fat diet-induced obesity [5].

In conclusion, Bcat2 plays a vital role in BCAA catabolism, and its function is closely related to the development of multiple diseases such as PDAC, melanoma, and colorectal cancer. The use of Bcat2 KO/CKO mouse models has significantly contributed to understanding its role in these disease areas, providing potential therapeutic targets and new insights into disease mechanisms.

References:
1. Li, Jin-Tao, Yin, Miao, Wang, Di, Su, Dan, Lei, Qun-Ying. 2020. BCAT2-mediated BCAA catabolism is critical for development of pancreatic ductal adenocarcinoma. In Nature cell biology, 22, 167-174. doi:10.1038/s41556-019-0455-6. https://pubmed.ncbi.nlm.nih.gov/32029896/
2. Tian, Yangzi, Ma, Jingjing, Wang, Hao, Guo, Weinan, Li, Chunying. 2023. BCAT2 promotes melanoma progression by activating lipogenesis via the epigenetic regulation of FASN and ACLY expressions. In Cellular and molecular life sciences : CMLS, 80, 315. doi:10.1007/s00018-023-04965-8. https://pubmed.ncbi.nlm.nih.gov/37801083/
3. Lei, Ming-Zhu, Li, Xu-Xu, Zhang, Ye, Qu, Jia, Lei, Qun-Ying. 2020. Acetylation promotes BCAT2 degradation to suppress BCAA catabolism and pancreatic cancer growth. In Signal transduction and targeted therapy, 5, 70. doi:10.1038/s41392-020-0168-0. https://pubmed.ncbi.nlm.nih.gov/32467562/
4. Wang, Yazhuo, Zhao, Ning, Meng, Yujiao, Li, Ping, Wang, Yan. 2024. Bcat2-Mediated Branched-Chain Amino Acid Catabolism Is Linked to the Aggravated Inflammation in Obese with Psoriasis Mice. In Molecular nutrition & food research, 68, e2300720. doi:10.1002/mnfr.202300720. https://pubmed.ncbi.nlm.nih.gov/38581348/
5. Ma, Qi-Xiang, Zhu, Wen-Ying, Lu, Xiao-Chen, Huang, Hai-Yan, Lei, Qun-Ying. 2022. BCAA-BCKA axis regulates WAT browning through acetylation of PRDM16. In Nature metabolism, 4, 106-122. doi:10.1038/s42255-021-00520-6. https://pubmed.ncbi.nlm.nih.gov/35075301/
6. Kang, Zi-Ran, Jiang, Shanshan, Han, Ji-Xuan, Chen, Huimin, Fang, Jing-Yuan. 2023. Deficiency of BCAT2-mediated branched-chain amino acid catabolism promotes colorectal cancer development. In Biochimica et biophysica acta. Molecular basis of disease, 1870, 166941. doi:10.1016/j.bbadis.2023.166941. https://pubmed.ncbi.nlm.nih.gov/37926361/
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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