Sqstm1-flox Mouse
Common Name
Sqstm1-flox
제품 ID
S-CKO-04127
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-18412-Sqstm1-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Sqstm1-flox Mouse (카탈로그 번호 S-CKO-04127)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
Sqstm1-flox
품종 계통계통 ID
CKOCMP-18412-Sqstm1-B6J-VA
유전자명
제품 ID
S-CKO-04127
유전자 별칭
Osi, p62, A170, STAP, OSF-6, STONE14
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 11
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000102774
NCBI 전사체 ID
NM_011018
타겟 영역
Exon 2~5
유효 영역 크기
~2.7 kb
유전자 연구 개요
Sqstm1, also known as p62, is a multifunctional scaffolding protein and a classical selective autophagy receptor [1,2,7]. It serves as an essential adaptor in selective autophagy, identifying and delivering specific organelles and protein aggregates to autophagosomes for degradation [2]. It is involved in various signaling pathways and plays a crucial role in maintaining cellular proteostasis, which is essential for somatic maintenance [7]. Genetic models such as knockout (KO) or conditional knockout (CKO) mouse models are valuable for studying its functions.
In vascular smooth muscle cells (VSMCs), Sqstm1 deficiency mimicked the phenotype of Ppargc1a depletion, presenting reduced autophagy and increased senescence both in vitro and in vivo. This suggests that Sqstm1 is a major regulator of autophagy and senescence in VSMCs and that the mitochondrial regulator PPARGC1A upregulates autophagy and reduces senescence through a Sqstm1 -dependent mechanism [3].
In the liver, liver-specific sqstm1-knockout mice showed that the SQSTM1-mediated noncanonical KEAP1-NFE2L2 pathway conferred hepatoprotection against lipotoxicity, indicating its importance in protecting the liver from lipotoxicity-related damage [4].
Disrupting the TRIB3-SQSTM1 interaction in mouse models of hepatic fibrosis restored autophagic flux in hepatocytes and hepatic stellate cells (HSCs), protecting against experimentally induced hepatic fibrosis [5].
Knockdown of Sqstm1 in the epidermis of a mouse model inhibited autophagy and delayed wound healing, highlighting its role in diabetic skin wound healing [6].
In conclusion, Sqstm1 is a pivotal player in selective autophagy, with its functions spanning across multiple biological processes such as autophagy regulation, senescence control, and protection against lipotoxicity and fibrosis. The use of KO/CKO mouse models has significantly contributed to understanding its role in diseases related to vascular senescence, fatty liver disease, hepatic fibrosis, and diabetic skin wound healing, providing insights into potential therapeutic strategies targeting these disease areas.
References:
1. Lamark, Trond, Svenning, Steingrim, Johansen, Terje. 2017. Regulation of selective autophagy: the p62/SQSTM1 paradigm. In Essays in biochemistry, 61, 609-624. doi:10.1042/EBC20170035. https://pubmed.ncbi.nlm.nih.gov/29233872/
2. Jeong, Se-Jin, Zhang, Xiangyu, Rodriguez-Velez, Astrid, Evans, Trent D, Razani, Babak. 2019. p62/SQSTM1 and Selective Autophagy in Cardiometabolic Diseases. In Antioxidants & redox signaling, 31, 458-471. doi:10.1089/ars.2018.7649. https://pubmed.ncbi.nlm.nih.gov/30588824/
3. Salazar, Gloria, Cullen, Abigail, Huang, Jingwen, Forouzandeh, Farshad, Hwang, Hyun Seok. 2019. SQSTM1/p62 and PPARGC1A/PGC-1alpha at the interface of autophagy and vascular senescence. In Autophagy, 16, 1092-1110. doi:10.1080/15548627.2019.1659612. https://pubmed.ncbi.nlm.nih.gov/31441382/
4. Lee, Da Hyun, Park, Jeong Su, Lee, Yu Seol, Lee, Yong-Ho, Bae, Soo Han. 2020. SQSTM1/p62 activates NFE2L2/NRF2 via ULK1-mediated autophagic KEAP1 degradation and protects mouse liver from lipotoxicity. In Autophagy, 16, 1949-1973. doi:10.1080/15548627.2020.1712108. https://pubmed.ncbi.nlm.nih.gov/31913745/
5. Zhang, Xiao-Wei, Zhou, Ji-Chao, Peng, Dian, Huang, Bo, Hu, Zhuo-Wei. 2019. Disrupting the TRIB3-SQSTM1 interaction reduces liver fibrosis by restoring autophagy and suppressing exosome-mediated HSC activation. In Autophagy, 16, 782-796. doi:10.1080/15548627.2019.1635383. https://pubmed.ncbi.nlm.nih.gov/31286822/
6. Liang, Diefei, Lin, Wei-Jye, Ren, Meng, Yan, Li, Wang, Wei. 2021. m6A reader YTHDC1 modulates autophagy by targeting SQSTM1 in diabetic skin. In Autophagy, 18, 1318-1337. doi:10.1080/15548627.2021.1974175. https://pubmed.ncbi.nlm.nih.gov/34657574/
7. Kumar, Anita V, Mills, Joslyn, Lapierre, Louis R. 2022. Selective Autophagy Receptor p62/SQSTM1, a Pivotal Player in Stress and Aging. In Frontiers in cell and developmental biology, 10, 793328. doi:10.3389/fcell.2022.793328. https://pubmed.ncbi.nlm.nih.gov/35237597/
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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