Srsf2-flox Mouse
一般名
Srsf2-flox
製品ID
S-CKO-18893
背景情報
C57BL/6JCya
系統ID
CKOCMP-20382-Srsf2-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Srsf2-flox Mouse(カタログ番号S-CKO-18893)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
Srsf2-flox
系統ID
CKOCMP-20382-Srsf2-B6J-VA
遺伝子名
製品ID
S-CKO-18893
遺伝子別名
SC35, MRF-1, Pr264, Sfrs2, Sfrs10, D11Wsu175e
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 11
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
ENSMUST00000092404
NCBIトランスクリプトID
NM_011358
ターゲット領域
Exon 1~2
有効領域の大きさ
~1.5 kb
遺伝子研究の概要
Srsf2, also known as SC35, is a serine/arginine-rich splicing factor widely expressed in mammalian cells. It plays vital roles in pre-mRNA processing and gene transcription, participating in numerous biological processes such as spermatogenesis, cell-cycle regulation, and DNA damage response [3,4]. It has also been implicated in disease-related pathways, especially in myelodysplastic syndromes (MDS) and myeloproliferative neoplasms (MPN) [1,2]. Genetic models, like KO/CKO mouse models, are valuable for studying its functions.
In male germ cell-specific Srsf2 knockout (Srsf2-deleted by Stra8-Cre), mice showed complete infertility and defective spermatogenesis. Srsf2 regulatory networks were found crucial for reproductive development, spermatogenesis, and related events. Srsf2 directly affected the expression and alternative splicing of genes encoding critical spermatogenesis factors [3].
In Srsf2P95H mutant knock-in mice co-expressed with Jak2V617F, reduced red blood cell, neutrophil, and platelet counts were observed, along with attenuated splenomegaly, without bone marrow fibrosis induction. Srsf2P95H also diminished the competitiveness of Jak2V617F mutant hematopoietic stem/progenitor cells [5].
Srsf2P95H in another set of knock-in mice delayed myelofibrosis induced by Jak2V617F, decreased TGFβ1 serum level, and reduced the competitiveness of transplanted Jak2V617F hematopoietic stem cells while preventing their exhaustion. RNA sequencing of megakaryocytes showed an increased number of splicing events when the two mutations were combined, with Srsf2P95H promoting Jak2 exon 14 skipping, generating an inactive JAK2 protein [6].
In conclusion, Srsf2 is essential for mRNA splicing during spermatogenesis and has a significant impact on hematopoietic functions as revealed through mouse model-based research. In disease areas, especially MDS and MPN, Srsf2 mutations play important roles, and studies using KO/CKO mouse models have provided insights into the molecular mechanisms underlying these diseases, which may help develop new therapeutic strategies.
References:
1. Kim, Eunhee, Ilagan, Janine O, Liang, Yang, Bradley, Robert K, Abdel-Wahab, Omar. . SRSF2 Mutations Contribute to Myelodysplasia by Mutant-Specific Effects on Exon Recognition. In Cancer cell, 27, 617-30. doi:10.1016/j.ccell.2015.04.006. https://pubmed.ncbi.nlm.nih.gov/25965569/
2. Aujla, Amandeep, Linder, Katherine, Iragavarapu, Chaitanya, Karass, Michael, Liu, Delong. 2018. SRSF2 mutations in myelodysplasia/myeloproliferative neoplasms. In Biomarker research, 6, 29. doi:10.1186/s40364-018-0142-y. https://pubmed.ncbi.nlm.nih.gov/30275952/
3. Lei, Wen-Long, Du, Zongchang, Meng, Tie-Gang, Qian, Wei-Ping, Sun, Qing-Yuan. 2023. SRSF2 is required for mRNA splicing during spermatogenesis. In BMC biology, 21, 231. doi:10.1186/s12915-023-01736-6. https://pubmed.ncbi.nlm.nih.gov/37867192/
4. Wagner, Rebecca E, Arnetzl, Leonie, Britto-Borges, Thiago, Bornelöv, Susanne, Frye, Michaela. 2024. SRSF2 safeguards efficient transcription of DNA damage and repair genes. In Cell reports, 43, 114869. doi:10.1016/j.celrep.2024.114869. https://pubmed.ncbi.nlm.nih.gov/39446588/
5. Yang, Yue, Abbas, Salar, Sayem, Mohammad A, Dutta, Avik, Mohi, Golam. 2023. SRSF2 mutation reduces polycythemia and impairs hematopoietic progenitor functions in JAK2V617F-driven myeloproliferative neoplasm. In Blood cancer journal, 13, 171. doi:10.1038/s41408-023-00947-y. https://pubmed.ncbi.nlm.nih.gov/38012156/
6. Willekens, Christophe, Laplane, Lucie, Dagher, Tracy, Vainchenker, William, Solary, Eric. 2023. SRSF2-P95H decreases JAK/STAT signaling in hematopoietic cells and delays myelofibrosis development in mice. In Leukemia, 37, 1287-1297. doi:10.1038/s41375-023-01878-0. https://pubmed.ncbi.nlm.nih.gov/37100881/
品質管理基準
精子検査
凍結前の精子濃度を測定し、精子の生存能力の判定します。
凍結後の精子では、各バッチから1本の凍結保存された精子を選び出し、体外受精に使用します。
環境基準:
SPF対応地域:
グローバル由来:
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