C57BL/6NCya-Bpgmem1/Cya
Common Name
Bpgm-KO
Product ID
S-KO-01248
Backgroud
C57BL/6NCya
Strain ID
KOCMP-12183-Bpgm-B6N-VA
When using this mouse strain in a publication, please cite “Bpgm-KO Mouse (Catalog S-KO-01248) were purchased from Cyagen.”
Product Type
Age
Genotype
Sex
Quantity
Basic Information
Strain Name
Bpgm-KO
Strain ID
KOCMP-12183-Bpgm-B6N-VA
Gene Name
Product ID
S-KO-01248
Gene Alias
--
Background
C57BL/6NCya
NCBI ID
Modification
Conventional knockout
Chromosome
Chr 6
Phenotype
Datasheet
Application
--
Strain Description
Ensembl Number
ENSMUST00000045372
NCBI RefSeq
NM_007563
Target Region
Exon 2~3
Size of Effective Region
~18.3 kb
Overview of Gene Research
Bpgm, short for bisphosphoglycerate mutase, is expressed in human erythrocytes and is responsible for the production of 2,3-bisphosphoglycerate (2,3-DPG), which plays a crucial role in modulating oxygen affinity to hemoglobin [1,2,3,4]. It is also involved in pathways related to glycolysis and metabolic reprogramming, thus having overall biological importance in processes like hypoxia response and energy regulation. Genetic models such as KO/CKO mouse models can be valuable for further exploring its functions.
In a mouse model, erythrocyte-specific deficiency in equilibrative nucleoside transporter 1 (eEnt1-/-) abolishes the activation of Bpgm, leading to reduced 2,3-bisphosphoglycerate and glutathione, overwhelming oxidative stress, and severe renal hypoxia, indicating its role in protecting against renal hypoxia and CKD progression [2]. In another study, inducible knockout of Bpgm in a tubular-specific, doxycycline-inducible Bpgm-knockout mouse model resulted in rapid kidney injury within 4 days, characterized by proximal tubular damage and tubulointerstitial fibrosis. Proteomic analyses revealed its involvement in key metabolic pathways, including glycolysis, oxidative stress response, and inflammation [4].
In summary, Bpgm is essential for the production of 2,3-DPG and is involved in multiple metabolic pathways. Studies using KO/CKO mouse models have revealed its critical role in maintaining kidney function and protecting against renal hypoxia-related diseases such as CKD [2,4].
References:
1. E, Guoji, Sun, Binda, Liu, Bao, Gao, Yuqi, Zhang, Erlong. 2022. Enhanced BPGM/2,3-DPG pathway activity suppresses glycolysis in hypoxic astrocytes via FIH-1 and TET2. In Brain research bulletin, 192, 36-46. doi:10.1016/j.brainresbull.2022.11.002. https://pubmed.ncbi.nlm.nih.gov/36334804/
2. Chen, Changhan, Xie, TingTing, Zhang, Yujin, D'Alessandro, Angelo, Xia, Yang. 2023. Erythrocyte ENT1-AMPD3 Axis is an Essential Purinergic Hypoxia Sensor and Energy Regulator Combating CKD in a Mouse Model. In Journal of the American Society of Nephrology : JASN, 34, 1647-1671. doi:10.1681/ASN.0000000000000195. https://pubmed.ncbi.nlm.nih.gov/37725437/
3. Qiang, Qingfen, Manalo, Jeanne M, Sun, Hong, D'Alessandro, Angelo, Xia, Yang. 2021. Erythrocyte adenosine A2B receptor prevents cognitive and auditory dysfunction by promoting hypoxic and metabolic reprogramming. In PLoS biology, 19, e3001239. doi:10.1371/journal.pbio.3001239. https://pubmed.ncbi.nlm.nih.gov/34138843/
4. Kulow, Vera A, Roegner, Kameliya, Labes, Robert, Rosenberger, Christian, Fähling, Michael. 2024. Beyond hemoglobin: Critical role of 2,3-bisphosphoglycerate mutase in kidney function and injury. In Acta physiologica (Oxford, England), 241, e14242. doi:10.1111/apha.14242. https://pubmed.ncbi.nlm.nih.gov/39422260/
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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