自线粒体化以来,亡因子在进化过程中得到了保存
Vandana Kaushal1, Joanna Klim1, Adrianna Skoneczna1
1Institute of Biochemistry and Biophysics PAS, Pawinskiego 5a, 02-106 Warszawa, Poland.
Genome biology and evolution
|August 24, 2023
概括
这项研究发现,来自细菌和多种真核生物的蛋白质可以触发酵母中的编程细胞死亡 (细胞亡),支持细胞亡的内共生起源及其古老的进化根源.
科学领域:
- 细胞生物学 细胞生物学
- 进化生物学 进化生物学
- 遗传学 遗传学 是一个
背景情况:
- 细胞死亡的apoptotic编程细胞死亡机制在真核生物中得到保护.
- 这些机制涉及线粒体透性过渡,激活蛋白酶,DNase和黄蛋白蛋白.
- 内共生理论提出,这些在线粒体化过程中从eubacteria毒素进化.
研究的目的:
- 调查细菌和远距离相关的真核体的正确基因是否可以替代酵母细胞亡因子.
- 为了测试 Апопто斯的内共生起源的假设.
主要方法:
- 酵母菌Saccharomyces cerevisiae的亡蛋白酶 (Mca1,Nma111,DNase (Nuc1) 和黄蛋白 (Ndi1) 的功能分析.
- 用植物,原生体和eubacteria的ortologs进行替换测试.
- 在酵母模型中通过化学应力诱导亡.
主要成果:
- 来自不同类型的真核生物和真核细菌的正义学家成功地在酵母菌中启动了亡.
- 证明了在巨大的进化距离上对亡因子的功能性保护.
- 证据支持自线粒体化 (约1800亿年前) 以来,古代维护了亡机制.
结论:
- 自线粒体化以来,亡机制在进化上得到了保存.
- 这些发现支持了一些亡因子起源于欧细菌毒素的假设.
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