Nrarp-KO Mouse
Common Name
Nrarp-KO
제품 ID
S-KO-12120
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-67122-Nrarp-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Nrarp-KO Mouse (카탈로그 번호 S-KO-12120)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
Nrarp-KO
품종 계통계통 ID
KOCMP-67122-Nrarp-B6J-VA
유전자명
제품 ID
S-KO-12120
유전자 별칭
2700054M22Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 2
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000104999
NCBI 전사체 ID
NM_025980
타겟 영역
Exon 1
유효 영역 크기
~2.9 kb
유전자 연구 개요
Nrarp, short for Notch-regulated ankyrin repeat protein, is a key gene that acts as a molecular link between the Notch and Wnt signaling pathways [3,4,8]. It contains two ankyrin repeats and its expression is transcriptionally regulated by the Notch signaling pathway [7]. Nrarp plays significant roles in multiple biological processes such as cell fate determination during embryogenesis, neural-crest-cell differentiation, osteoblastogenesis, and angiogenesis [4,5,6,8].
In T-cell acute lymphoblastic leukemia (T-ALL), Nrarp shows a dual role. Overexpression of Nrarp can block NOTCH1 signaling and delay the proliferation of T-ALL cells with high Notch1 signaling, but promote the expansion of those with lower Notch1 activity. It interacts with lymphoid enhancer-binding factor 1 (LEF1) and potentiates Wnt signaling in T-ALL cells with low Notch levels [1]. In reninoma, structural variants lead to the removal of NRARP while generating canonical activating rearrangements of NOTCH1, indicating dysregulated Notch pathway signalling [2]. In breast cancer cells, downregulation of NRARP exerts anti-tumor activities through Wnt/β-catenin-mediated signals, and miR-130a-3p can inhibit NRARP expression to achieve this [3]. In zebrafish, knockdown of Nrarp-a affects Wnt-signalling-dependent neural-crest-cell development by regulating LEF1 protein stability [4]. In osteoblasts, miR-487b-3p impairs osteoblastogenesis by targeting Nrarp, which in turn suppresses Runx-2 and Wnt signaling [6]. In angiogenesis, loss of Nrarp, Lef1, or endothelial Ctnnb1 causes vessel regression as Nrarp coordinates endothelial Notch and Wnt signaling to control vessel density [8].
In conclusion, Nrarp is crucial in coordinating Notch and Wnt signaling pathways across different biological processes. Its study through gene knockdown or knockout models in organisms like mice and zebrafish has revealed its significance in diseases such as T-ALL, reninoma, and breast cancer, as well as in normal developmental processes like neural-crest-cell differentiation, osteoblastogenesis, and angiogenesis.
References:
1. Pinto, Inês, Duque, Mafalda, Gonçalves, Joana, Barata, João T, Fragoso, Rita. 2019. NRARP displays either pro- or anti-tumoral roles in T-cell acute lymphoblastic leukemia depending on Notch and Wnt signaling. In Oncogene, 39, 975-986. doi:10.1038/s41388-019-1042-9. https://pubmed.ncbi.nlm.nih.gov/31586130/
2. Treger, Taryn D, Lawrence, John E G, Anderson, Nathaniel D, Behjati, Sam, Chowdhury, Tanzina. 2023. Targetable NOTCH1 rearrangements in reninoma. In Nature communications, 14, 5826. doi:10.1038/s41467-023-41118-8. https://pubmed.ncbi.nlm.nih.gov/37749094/
3. Poodineh, Jafar, Sirati-Sabet, Majid, Rajabibazl, Masoumeh, Ghasemian, Majid, Mohammadi-Yeganeh, Samira. 2022. Downregulation of NRARP exerts anti-tumor activities in the breast tumor cells depending on Wnt/β-catenin-mediated signals: The role of miR-130a-3p. In Chemical biology & drug design, 100, 334-345. doi:10.1111/cbdd.14113. https://pubmed.ncbi.nlm.nih.gov/35797350/
4. Ishitani, Tohru, Matsumoto, Kunihiro, Chitnis, Ajay B, Itoh, Motoyuki. . Nrarp functions to modulate neural-crest-cell differentiation by regulating LEF1 protein stability. In Nature cell biology, 7, 1106-12. doi:. https://pubmed.ncbi.nlm.nih.gov/16228014/
5. Lamar, E, Deblandre, G, Wettstein, D, Niehrs, C, Kintner, C. . Nrarp is a novel intracellular component of the Notch signaling pathway. In Genes & development, 15, 1885-99. doi:. https://pubmed.ncbi.nlm.nih.gov/11485984/
6. John, Aijaz A, Prakash, Ravi, Singh, Divya. . miR-487b-3p impairs osteoblastogenesis by targeting Notch-regulated ankyrin-repeat protein (Nrarp). In The Journal of endocrinology, 241, 249-263. doi:10.1530/JOE-19-0015. https://pubmed.ncbi.nlm.nih.gov/30978699/
7. Krebs, L T, Deftos, M L, Bevan, M J, Gridley, T. . The Nrarp gene encodes an ankyrin-repeat protein that is transcriptionally regulated by the notch signaling pathway. In Developmental biology, 238, 110-9. doi:. https://pubmed.ncbi.nlm.nih.gov/11783997/
8. Phng, Li-Kun, Potente, Michael, Leslie, Jonathan D, Thurston, Gavin, Gerhardt, Holger. . Nrarp coordinates endothelial Notch and Wnt signaling to control vessel density in angiogenesis. In Developmental cell, 16, 70-82. doi:10.1016/j.devcel.2008.12.009. https://pubmed.ncbi.nlm.nih.gov/19154719/
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:
Cyagen문의하기
맞춤형 동물 모델 관련 상담을 위해 Cyagen 전문가와 연락해 보세요. 아래 양식을 작성하여 상담을 시작하거나 견적을 요청하시기 바랍니다.
Cyagen은 고객님의 개인정보를 소중히 여깁니다. 최신 제품, 서비스 및 인사이트를 안내드리고자 합니다. 고객님의 수신 설정은 다음과 같습니다:
해당 커뮤니케이션은 언제든지 수신 거부하실 수 있습니다. 수신 거부 방법 및 데이터 보호에 대한 자세한 내용은 개인정보처리방침을 참고해 주시기 바랍니다.
아래 버튼을 클릭함으로써, 요청하신 콘텐츠 제공을 위해 본 양식을 통해 제출된 개인정보를 Cyagen이 저장 및 처리하는 데 동의하게 됩니다.
