Scin-KO Mouse
Common Name
Scin-KO
제품 ID
S-KO-04206
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-20259-Scin-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Scin-KO Mouse (카탈로그 번호 S-KO-04206)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
기본 정보
품종 계통
Scin-KO
품종 계통계통 ID
KOCMP-20259-Scin-B6J-VA
유전자명
제품 ID
S-KO-04206
유전자 별칭
adseverin
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 12
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000002640
NCBI 전사체 ID
NM_001146196
타겟 영역
Exon 2~3
유효 영역 크기
~5.9 kb
유전자 연구 개요
SCIN, also known as scinderin, is a calcium-dependent actin severing and capping protein. It is involved in regulating the F-actin cytoskeleton network, which is crucial for maintaining cell polarity, adhesion, proliferation, and migration. These functions are associated with various biological processes and disease-related pathways [5,7]. Genetic models, such as gene knockout mouse models, can be valuable for studying its functions.
In a conditional knockout (cKO) mouse model where the gene encoding the catalytic subunit Pik3c3 was specifically deleted in Sertoli cells, an accumulation of SCIN was observed. This led to the disorder and disassembly of the F-actin cytoskeleton, disrupting Sertoli cell polarity and impairing spermiogenesis. The results suggest that PIK3C3 negatively regulates SCIN, and the autophagy-lysosome pathway is involved in SCIN degradation [1]. In cancer-related studies, in gastric cancer, overexpressing miR-301a-5p promoted cell proliferation and motility by targeting SCIN, affecting the epithelial-mesenchymal transition (EMT) progression via STAT3 and NF-κB signaling [2]. In nasopharyngeal carcinoma, MEX3A promoted cancer progression via the miR-3163/SCIN axis by regulating NF-κB signaling. Depletion of SCIN reversed the oncogenic effects of MEX3A [3]. Lentivirus-mediated silencing of SCIN in human lung carcinoma cells inhibited cell proliferation, induced G0/G1 phase cell cycle arrest, and increased the expression of Cyclin B1, p21 and PARP [5]. Similar effects were seen in prostate cancer cells, where silencing of SCIN inhibited proliferation and induced G0/G1 cell cycle arrest through the regulation of cell cycle-related genes [7]. In triple-negative breast cancer, RSRC2 transcriptionally inhibited SCIN expression, and re-expression of SCIN reversed the cellular function changes caused by RSRC2 [6]. In acute myeloid leukemia, decreased SCIN expression associated with promoter methylation was a valuable biomarker for predicting adverse prognosis [4].
In conclusion, SCIN plays essential roles in maintaining the actin cytoskeleton and cell functions such as proliferation and cell cycle regulation. The use of KO/CKO mouse models and other loss-of-function experiments has revealed its significance in spermatogenesis and various cancer-related processes, providing insights into potential therapeutic targets for infertility and cancer treatment.
References:
1. Wang, Kehan, Kong, Feifei, Qiu, Yuexin, Hu, Zhibin, Li, Jing. 2023. Autophagy regulation and protein kinase activity of PIK3C3 controls sertoli cell polarity through its negative regulation on SCIN (scinderin). In Autophagy, 19, 2934-2957. doi:10.1080/15548627.2023.2235195. https://pubmed.ncbi.nlm.nih.gov/37450577/
2. Huang, Yingying, Du, Xiaoxiao, Chen, Xiangliu, Yang, Yan, Teng, Lisong. 2021. MiR-301a-5p/SCIN promotes gastric cancer progression via regulating STAT3 and NF-κB signaling. In Journal of Cancer, 12, 5394-5403. doi:10.7150/jca.59747. https://pubmed.ncbi.nlm.nih.gov/34405002/
3. Xiang, Xin-Xin, Liu, Yong-Liang, Kang, Yi-Fan, Lu, Xiang, Xu, Kai. 2022. MEX3A promotes nasopharyngeal carcinoma progression via the miR-3163/SCIN axis by regulating NF-κB signaling pathway. In Cell death & disease, 13, 420. doi:10.1038/s41419-022-04871-0. https://pubmed.ncbi.nlm.nih.gov/35490173/
4. Zhang, Zhi-Hui, Zhang, Wei, Zhou, Jing-Dong, Lin, Jiang, Qian, Jun. 2018. Decreased SCIN expression, associated with promoter methylation, is a valuable predictor for prognosis in acute myeloid leukemia. In Molecular carcinogenesis, 57, 735-744. doi:10.1002/mc.22794. https://pubmed.ncbi.nlm.nih.gov/29457658/
5. Liu, Hongxu, Shi, Daiwang, Liu, Tieqin, Yu, Zhanwu, Zhou, Chuanjiang. 2014. Lentivirus-mediated silencing of SCIN inhibits proliferation of human lung carcinoma cells. In Gene, 554, 32-9. doi:10.1016/j.gene.2014.10.013. https://pubmed.ncbi.nlm.nih.gov/25303873/
6. Zhao, Nan, Ni, Chunsheng, Fan, Shuai, Zhao, Xiulan, Liu, Tieju. 2023. RSRC2 Expression Inhibits Malignant Progression of Triple-Negative Breast Cancer by Transcriptionally Regulating SCIN Expression. In Cancers, 16, . doi:10.3390/cancers16010015. https://pubmed.ncbi.nlm.nih.gov/38201443/
7. Wang, Dong, Sun, Shu-Qing, Yu, Ying-Hao, Yang, Shun-Liang, Tan, Jian-Ming. 2013. Suppression of SCIN inhibits human prostate cancer cell proliferation and induces G0/G1 phase arrest. In International journal of oncology, 44, 161-6. doi:10.3892/ijo.2013.2170. https://pubmed.ncbi.nlm.nih.gov/24212916/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
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