在携带SRSF4基因变异的患者中,线粒体功能受损和骨髓衰竭
Maurizio Miano1, Nadia Bertola2, Alice Grossi3
1Haematology Unit, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.
International journal of molecular sciences
|February 24, 2024
概括
一种新的SRSF4基因变异通过损害线粒体功能和能量代谢导致骨髓衰竭. 恢复SRSF4蛋白水平纠正了这些缺陷,突出了其在血液形成中的作用.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 细胞生物学 细胞生物学
背景情况:
- 富含氨酸/氨酸的拼接因子 (SRSFs) 调节RNA拼接,已知SRSF6会影响线粒体活动.
- 以前没有报告SRSF4在骨髓衰竭中的作用及其与线粒体功能障碍的直接联系.
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