C57BL/6JCya-Plbd1em1/Cya
Common Name:
Plbd1-KO
Product ID:
S-KO-11953
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
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Basic Information
Strain Name
Plbd1-KO
Strain ID
KOCMP-66857-Plbd1-B6J-VA
Gene Name
Product ID
S-KO-11953
Gene Alias
1100001H23Rik
Background
C57BL/6JCya
NCBI ID
Modification
Conventional knockout
Chromosome
6
Phenotype
Document
Application
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Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Plbd1em1/Cya mice (Catalog S-KO-11953) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000032336
NCBI RefSeq
NM_025806
Target Region
Exon 2
Size of Effective Region
~2.9 kb
Detailed Document
Overview of Gene Research
Plbd1, or Phospholipase B domain-containing protein 1, is a transcription factor that regulates phospholipid metabolism [2]. It may be involved in lysosomal functions as it was identified as one of the hub lysosomal genes closely linked to psoriasis occurrence [3].
In ischemic stroke models, Plbd1 was significantly upregulated in affected brain tissues and cells. Knockdown of Plbd1 mitigated cellular injury in vitro and reversed brain damage in vivo, indicating its role in exacerbating ischemic stroke-induced brain damage. Lactylation at the K155 site of Plbd1 enhanced its expression in response to elevated lactate levels after oxygen-glucose deprivation and reperfusion treatment [1]. In glioma, high expression of Plbd1 was observed, and knockdown of it significantly inhibited the proliferation and invasive ability of glioma cells, suggesting it could be a potential tumor prognostic biomarker and immunotherapeutic target [2]. Also, in acute myocardial infarction patients, peripheral blood RNA levels of Plbd1 were new independent predictors of left ventricular dysfunction post-MI [4].
In summary, Plbd1 plays important roles in multiple disease conditions. Its upregulation via lactylation at the K155 site exacerbates ischemic stroke-induced brain damage. In glioma, it is involved in cell proliferation and invasion, and in acute myocardial infarction, it can predict left ventricular dysfunction. The study of Plbd1 using gene knockout or other loss-of-function models helps to understand its functions in these diseases, potentially providing new therapeutic strategies.
References:
1. Zhou, Faming, Chen, Guanghui, Li, Xiaoli, Yu, Xiaodong, Yang, Yinyin. . Lactylation of PLBD1 Facilitates Brain Injury Induced by Ischemic Stroke. In Journal of integrative neuroscience, 24, 25949. doi:10.31083/JIN25949. https://pubmed.ncbi.nlm.nih.gov/40018779/
2. Wei, Minghao, Zhou, Gaoyang, Chen, Lian, Gao, Li, Gao, Guodong. 2024. The prognostic and immune significance of PLBD1 in pan-cancer and its roles in proliferation and invasion of glioma. In Journal of Cancer, 15, 3857-3872. doi:10.7150/jca.96365. https://pubmed.ncbi.nlm.nih.gov/38911364/
3. Deng, Wenhui, Yan, Yijiao, Shi, Chengzhi, Sui, Daoshun. 2024. Single-cell and bulk RNAseq unveils the immune infiltration landscape and targeted therapeutic biomarkers of psoriasis. In Frontiers in genetics, 15, 1365273. doi:10.3389/fgene.2024.1365273. https://pubmed.ncbi.nlm.nih.gov/38699235/
4. Vanhaverbeke, Maarten, Vausort, Mélanie, Veltman, Denise, Janssens, Stefan, Sinnaeve, Peter R. 2019. Peripheral Blood RNA Levels of QSOX1 and PLBD1 Are New Independent Predictors of Left Ventricular Dysfunction After Acute Myocardial Infarction. In Circulation. Genomic and precision medicine, 12, e002656. doi:10.1161/CIRCGEN.119.002656. https://pubmed.ncbi.nlm.nih.gov/31756302/
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