Rnf220-flox Mouse
一般名
Rnf220-flox
製品ID
S-CKO-13276
背景情報
C57BL/6JCya
系統ID
CKOCMP-66743-Rnf220-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Rnf220-flox Mouse(カタログ番号S-CKO-13276)はサイアジェンから購入しました。」と引用してください。
製品タイプ
年齢
遺伝子型
性別
数量
標準的な配送方法では、少なくとも3匹のヘテロ接合体キャリアを保証しています。ホモ接合体キャリアや指定された性別の個体の繁殖サービスも利用可能です。
基本情報
系統名
Rnf220-flox
系統ID
CKOCMP-66743-Rnf220-B6J-VA
遺伝子名
製品ID
S-CKO-13276
遺伝子別名
4732477A13, 4931406I20Rik, 5730503K05Rik
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 4
表現型
アプリケーション
--
さらに
系統詳細
EnsemblトランスクリプトID
ENSMUST00000030439
NCBIトランスクリプトID
NM_025739
ターゲット領域
Exon 2
有効領域の大きさ
~1.5 kb
遺伝子研究の概要
Rnf220, also known as Ring finger protein 220, is an evolutionarily conserved RING-type ubiquitin E3 ligase. It plays crucial roles in multiple cellular processes, participating in various signaling pathways such as Shh, Wnt, and IFN-STAT1 signaling, which are essential for vertebrate embryo development, cell differentiation, and immune response [5].
In mouse models, Rnf220 knockout specifically increases AMPAR protein levels, enhancing basal synaptic activity while impairing synaptic plasticity, and also altering learning and memory in forebrain-deficient mice, indicating its role in excitatory synaptic transmission [1]. Rnf220 depletion in oligodendrocyte lineage cells in mice impedes oligodendrocyte progenitor cell proliferation, differentiation, and (re)myelination, leading to learning and memory defects, highlighting its importance in oligodendroglial development [2]. Rnf220-deficient mice show down-regulation of IFN signaling and decreased expression of ISGs in response to infections, demonstrating its role in innate immune responses [3]. In Rnf220-deficient mice, the development of central NA neurons is affected as genes associated with LC-NA neurons are not properly maintained [4]. Nestin-Cre-mediated conditional knockout (Rnf220 Nestin CKO) mice show alterations in progenitor domains in the ventral VZ of the hindbrain, revealing its role in hindbrain dorsoventral patterning [6]. RNF220 +/ -; Ptch1 +/-mice have lower spontaneous medulloblastoma occurrence compared with Ptch1 +/-mice, suggesting its role in medulloblastoma progression [7]. Overexpression of RNF220 promotes the proliferation of AML cells in vitro [8].
In conclusion, Rnf220 is a multifunctional E3 ubiquitin ligase involved in neural development, immune response, and cancer progression. Gene knockout and conditional knockout mouse models have been instrumental in uncovering its role in excitatory synaptic transmission, oligodendroglial development, innate immune responses, central NA neuron development, hindbrain patterning, and cancer-related processes, providing insights into the underlying mechanisms of related diseases.
References:
1. Ma, Pengcheng, Wan, Li Pear, Li, Yuwei, Mao, Bingyu, Sheng, Nengyin. 2022. RNF220 is an E3 ubiquitin ligase for AMPA receptors to regulate synaptic transmission. In Science advances, 8, eabq4736. doi:10.1126/sciadv.abq4736. https://pubmed.ncbi.nlm.nih.gov/36179027/
2. Li, Yuwei, Wan, Li Pear, Song, Ning-Ning, Sheng, Nengyin, Ma, Pengcheng. 2024. RNF220-mediated K63-linked polyubiquitination stabilizes Olig proteins during oligodendroglial development and myelination. In Science advances, 10, eadk3931. doi:10.1126/sciadv.adk3931. https://pubmed.ncbi.nlm.nih.gov/38324685/
3. Guo, Xiaomin, Ma, Pengcheng, Li, Yuwei, Mao, Bingyu, Qi, Xiaopeng. 2020. RNF220 mediates K63-linked polyubiquitination of STAT1 and promotes host defense. In Cell death and differentiation, 28, 640-656. doi:10.1038/s41418-020-00609-7. https://pubmed.ncbi.nlm.nih.gov/32814877/
4. Song, Ning-Ning, Ma, Pengcheng, Zhang, Qiong, Mao, Bingyu, Ding, Yu-Qiang. 2020. Rnf220/Zc4h2-mediated monoubiquitylation of Phox2 is required for noradrenergic neuron development. In Development (Cambridge, England), 147, . doi:10.1242/dev.185199. https://pubmed.ncbi.nlm.nih.gov/32094113/
5. Ma, Pengcheng, Mao, Bingyu. 2021. The many faces of the E3 ubiquitin ligase, RNF220, in neural development and beyond. In Development, growth & differentiation, 64, 98-105. doi:10.1111/dgd.12756. https://pubmed.ncbi.nlm.nih.gov/34716995/
6. Wang, Yu-Bing, Song, Ning-Ning, Zhang, Lei, Mao, Bingyu, Ding, Yu-Qiang. 2022. Rnf220 is Implicated in the Dorsoventral Patterning of the Hindbrain Neural Tube in Mice. In Frontiers in cell and developmental biology, 10, 831365. doi:10.3389/fcell.2022.831365. https://pubmed.ncbi.nlm.nih.gov/35399523/
7. Ma, Pengcheng, An, Tao, Zhu, Liang, Li, Yan, Mao, Bingyu. 2020. RNF220 is required for cerebellum development and regulates medulloblastoma progression through epigenetic modulation of Shh signaling. In Development (Cambridge, England), 147, . doi:10.1242/dev.188078. https://pubmed.ncbi.nlm.nih.gov/32376680/
8. Pan, Yuming, An, Na, Deng, Xiaopeng, Zhang, Qiaoxia, Du, Xin. 2020. RNF220 promotes the proliferation of leukaemic cells and reduces the degradation of the Cyclin D1 protein through USP22. In Blood cells, molecules & diseases, 86, 102490. doi:10.1016/j.bcmd.2020.102490. https://pubmed.ncbi.nlm.nih.gov/32896826/
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