酵母基因KTI13 (又名DPH8) 在二胺合成的启动步骤中运行在延长因子2上
Meike Arend1, Koray Ütkür1, Harmen Hawer1
1Institute of Biology, Division of Microbiology, University of Kassel, Heinrich-Plett-Str. 40, 34132 Kassel, Germany.
Microbial cell (Graz, Austria)
|September 4, 2023
概括
Kti11•Kti13二聚体调节酵母中的tRNA修饰,并参与二胺修饰延长因子2 (EF2). 在EF2.2上,Kti13对于diphthamide合成的初始步骤至关重要.
科学领域:
- 分子生物学分子生物学
- 酵母遗传学 酵母遗传学
背景情况:
- 延长器依赖的tRNA修饰是由Kti11•Kti13二次体调节的.
- 这种二聚体也是齐摩辛的目标,这是一种杀死细胞的利博毒素.
- 众所周知,Kti11 (Dph3) 可以控制二胺基对延长因子2 (EF2) 的修饰.
研究的目的:
- 调查Kti13在EF2.2的二胺基修饰中的作用.
- 了解Kti11•Kti13二次元在EF2修改中的功能.
主要方法:
- 酵母遗传学 (Δ无突变的基因).
- 质谱测量 质谱测量 质谱测量
- 通过喉毒素 (DT) 检测ADP-ribosylation和通过sordarin.inhibition进行检测.
主要成果:
- kti13Δ突变体具有未经修改的EF2,对DT和sordarin有抗性.
- 质谱检测揭示了二胺基形成的第一步 (氨基----EF2) 的阻断.
- 在启动EF2修改时,Kti11/Dph3和Kti13共享角色.
结论:
- 在EF2.2上,Kti13对于启动二胺合成至关重要.
- 在tRNA和EF2修改中,Kti11/Dph3和Kti13具有双重功能.
- 拟议的名称KTI13/DPH8反映了其双重作用,类似于KTI11/DPH3.
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