C57BL/6JCya-Cpne7em1flox/Cya
Common Name:
Cpne7-flox
Product ID:
S-CKO-19082
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
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Basic Information
Strain Name
Cpne7-flox
Strain ID
CKOCMP-102278-Cpne7-B6J-VB
Gene Name
Product ID
S-CKO-19082
Gene Alias
-
Background
C57BL/6JCya
NCBI ID
Modification
Conditional knockout
Chromosome
8
Phenotype
Document
Application
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Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Cpne7em1flox/Cya mice (Catalog S-CKO-19082) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000037900
NCBI RefSeq
NM_170684
Target Region
Exon 3~10
Size of Effective Region
~5.1 kb
Detailed Document
Overview of Gene Research
Cpne7, also known as copine-7, is involved in multiple biological processes. It plays a crucial role in the maintenance and homeostasis of odontoblasts, promoting their differentiation from progenitor cells. It also impacts periodontal ligament regeneration. In addition, Cpne7 is associated with the regulation of amyloidogenesis in Alzheimer's disease and is implicated in colorectal tumorigenesis [1,2,4,3].
In the dental pulp, Cpne7 -null mice exhibit accelerated cellular senescence in odontoblasts due to oxidative stress and DNA damage accumulation, leading to impaired odontoblast survival and aberrant dentin formation [1]. In contrast, Cpne7 -overexpressing transgenic mice show a healthy dentin-pulp complex and physiologic dentin regeneration. In colorectal cancer, knockdown of Cpne7 inhibits cell proliferation, colony formation, and metastasis, while promoting apoptosis. Delivery of Cpne7 shRNA hinders tumor growth in vivo [3,5,6].
In conclusion, Cpne7 is essential for maintaining the proper function of odontoblasts and periodontal tissues. In disease areas, Cpne7 plays a significant role in colorectal tumorigenesis, and its knockdown can enhance the chemosensitivity of colorectal cancer cells. The study of Cpne7 using gene knockout models has provided valuable insights into its function in dental and cancer-related biological processes.
References:
1. Lee, Yoon Seon, Park, Yeoung-Hyun, Hwang, Geumbit, Lee, Gene, Park, Joo-Cheol. 2023. Cpne7 deficiency induces cellular senescence and premature aging of dental pulp. In Aging cell, 23, e14061. doi:10.1111/acel.14061. https://pubmed.ncbi.nlm.nih.gov/38105557/
2. Bai, Shengfeng, Lee, Ji-Hyun, Son, Chul, Lee, Dong-Seol, Park, Joo-Cheol. 2022. CPNE7 regenerates periodontal ligament via TAU-mediated alignment and cementum attachment protein-mediated attachment. In Journal of clinical periodontology, 49, 609-620. doi:10.1111/jcpe.13621. https://pubmed.ncbi.nlm.nih.gov/35373365/
3. Zhao, Liangbo, Sun, Xiao, Hou, Chenying, Jin, Shuiling, Liu, Benyu. 2024. CPNE7 promotes colorectal tumorigenesis by interacting with NONO to initiate ZFP42 transcription. In Cell death & disease, 15, 896. doi:10.1038/s41419-024-07288-z. https://pubmed.ncbi.nlm.nih.gov/39695095/
4. Yang, Jie, Pu, Ya-Lan, Pan, Qiu-Lin, Zhu, Bing-Lin, Chen, Guo-Jun. . CPNE7 Regulates Amyloidogenesis Through CAP1-Dependent ADAM10 Translation. In Journal of neurochemistry, 169, e70026. doi:10.1111/jnc.70026. https://pubmed.ncbi.nlm.nih.gov/40026213/
5. Xu, Weile, Tang, Yujie, Yang, Yang, Zhao, Lianmei, Wang, Guiying. . Depletion of CPNE7 sensitizes colorectal cancer to 5-fluorouracil by downregulating ATG9B expression. In Journal of cellular and molecular medicine, 28, e18261. doi:10.1111/jcmm.18261. https://pubmed.ncbi.nlm.nih.gov/38526029/
6. Kong, Hye-Jeong, Kang, Dong-Hyun, Ahn, Tae-Sung, Ryu, Jae-Sung, Beak, Moo-Jun. 2023. The Role of CPNE7 (Copine-7) in Colorectal Cancer Prognosis and Metastasis. In International journal of molecular sciences, 24, . doi:10.3390/ijms242316704. https://pubmed.ncbi.nlm.nih.gov/38069026/
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