Rhoa-flox Mouse
Common Name
Rhoa-flox
제품 ID
S-CKO-01297
Backgroud
C57BL/6NCya
품종 계통계통 ID
CKOCMP-11848-Rhoa-B6N-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Rhoa-flox Mouse (카탈로그 번호 S-CKO-01297)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
Rhoa-flox
품종 계통계통 ID
CKOCMP-11848-Rhoa-B6N-VA
유전자명
제품 ID
S-CKO-01297
유전자 별칭
Arha, Arha1, Arha2
배경
C57BL/6NCya
유전자 공식 전체 명칭
ras homolog family member A
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 9
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000007959
NCBI 전사체 ID
NM_016802
타겟 영역
Exon 4
유효 영역 크기
~1.2 kb
유전자 연구 개요
RhoA, short for Ras homolog gene family member A, is a small GTPase of the Rho family. It is a key regulator of cytoskeletal dynamics and is involved in multiple signal transduction pathways, influencing various cellular functions such as cell survival, migration, adhesion, and proliferation [1,2]. RhoA and its downstream effector proteins are highly expressed in the nervous system, suggesting a significant role in neurons and glial cells [1]. The RhoA/ROCK signaling pathway is associated with many neuronal functions and central nervous system diseases [3,4].
In neurodegenerative diseases like Parkinson's, Alzheimer's, Huntington's, and amyotrophic lateral sclerosis, aberrant RhoA signaling has been implicated [1]. In Alzheimer's disease, the RhoA/ROCK signaling pathway promotes the disease occurrence by increasing β -secretase activity, promoting amyloid-beta production, and forming neurofibrillary tangles [4]. In ischemic stroke, the RhoA/ROCK signaling pathway and astrocytes play roles in neurological function and tissue repair after brain injury [3]. In hematological cancers, deregulated RHOA activity is linked to cancer growth, progression, and metastasis, and RHOA may have both tumor-promoting and tumor-suppressive functions depending on the context [2]. In capillary malformation-arteriovenous malformation syndrome, loss of RASA1 may lead to constitutive activation of RhoA signaling, increasing vascular permeability [5]. Also, RhoA is crucial for myoblast fusion during muscle regeneration and hypertrophy, and is involved in DNA damage response, mediating cell cycle arrest [6,7].
In conclusion, RhoA is a vital regulator of numerous cellular functions and is involved in various biological processes and disease conditions. Studies on RhoA, especially those using gene knockout or conditional knockout mouse models (although not explicitly detailed in the provided abstracts but inferred from the research context), have enhanced our understanding of its functions in neurodegenerative diseases, cancers, and other disorders, providing potential therapeutic targets for these diseases.
References:
1. Schmidt, Sissel Ida, Blaabjerg, Morten, Freude, Kristine, Meyer, Morten. 2022. RhoA Signaling in Neurodegenerative Diseases. In Cells, 11, . doi:10.3390/cells11091520. https://pubmed.ncbi.nlm.nih.gov/35563826/
2. Santos, Juliana Carvalho, Profitós-Pelejà, Núria, Sánchez-Vinces, Salvador, Roué, Gaël. 2023. RHOA Therapeutic Targeting in Hematological Cancers. In Cells, 12, . doi:10.3390/cells12030433. https://pubmed.ncbi.nlm.nih.gov/36766776/
3. Lu, Weizhuo, Chen, Zhiwu, Wen, Jiyue. 2021. RhoA/ROCK signaling pathway and astrocytes in ischemic stroke. In Metabolic brain disease, 36, 1101-1108. doi:10.1007/s11011-021-00709-4. https://pubmed.ncbi.nlm.nih.gov/33745103/
4. Cai, RuoLan, Wang, YangYang, Huang, ZhenTing, Yu, Changyin, Cai, Zhiyou. 2021. Role of RhoA/ROCK signaling in Alzheimer's disease. In Behavioural brain research, 414, 113481. doi:10.1016/j.bbr.2021.113481. https://pubmed.ncbi.nlm.nih.gov/34302876/
5. Eisa-Beygi, Shahram, Vo, Nghia Jack, Link, Brian A. 2020. RhoA activation-mediated vascular permeability in capillary malformation-arteriovenous malformation syndrome: a hypothesis. In Drug discovery today, 26, 1790-1793. doi:10.1016/j.drudis.2020.12.012. https://pubmed.ncbi.nlm.nih.gov/33358701/
6. Noviello, Chiara, Kobon, Kassandra, Randrianarison-Huetz, Voahangy, Falcone, Sestina, Sotiropoulos, Athanassia. 2023. RhoA Is a Crucial Regulator of Myoblast Fusion. In Cells, 12, . doi:10.3390/cells12232673. https://pubmed.ncbi.nlm.nih.gov/38067102/
7. Cheng, Chibin, Seen, Daniel, Zheng, Chunwen, Zeng, Ruijie, Li, Enmin. 2021. Role of Small GTPase RhoA in DNA Damage Response. In Biomolecules, 11, . doi:10.3390/biom11020212. https://pubmed.ncbi.nlm.nih.gov/33546351/
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:
Cyagen출판물
Neural Regeneration Research
2023-12
Motor neuron-specific RhoA knockout delays degeneration and promotes regeneration of dendrites in spinal ventral horn after brachial plexus injury
자세히 보기
Glia
2023-03-26
Schwann cell-specific RhoA knockout accelerates peripheral nerve regeneration via promoting Schwann cell dedifferentiation
자세히 보기
Journal of Neuroinflammation
2021-10-14
Macrophage-specific RhoA knockout delays Wallerian degeneration after peripheral nerve injury in mice
자세히 보기
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