Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou Medical University, Guangzhou, China; Centre for Regenerative Medicine and Health, Hong Kong Institute of Science & Innovation, Chinese Academy of Sciences, Hong Kong, SAR, China; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangdong-Hong Kong Joint Laboratory for Stem Cell and Regenerative Medicine, China-New Zealand Joint Laboratory on Biomedicine and Health, CUHK-GIBH Joint Research Laboratory on Stem Cells and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Institute for Stem Cell and Regeneration, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China; University of Chinese Academy of Sciences, Beijing, China.
Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou Medical University, Guangzhou, China; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangdong-Hong Kong Joint Laboratory for Stem Cell and Regenerative Medicine, China-New Zealand Joint Laboratory on Biomedicine and Health, CUHK-GIBH Joint Research Laboratory on Stem Cells and Regenerative Medicine, GIBH-HKU Guangdong-Hong Kong Stem Cell and Regenerative Medicine Research Centre, Institute for Stem Cell and Regeneration, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Cell Metab. 2024 Jul 2;36(7):1586-1597.e7. doi: 10.1016/j.cmet.2024.04.012. Epub 2024 May 3.
The mitochondrial genome transcribes 13 mRNAs coding for well-known proteins essential for oxidative phosphorylation. We demonstrate here that cytochrome b (CYTB), the only mitochondrial-DNA-encoded transcript among complex III, also encodes an unrecognized 187-amino-acid-long protein, CYTB-187AA, using the standard genetic code of cytosolic ribosomes rather than the mitochondrial genetic code. After validating the existence of this mtDNA-encoded protein arising from cytosolic translation (mPACT) using mass spectrometry and antibodies, we show that CYTB-187AA is mainly localized in the mitochondrial matrix and promotes the pluripotent state in primed-to-naive transition by interacting with solute carrier family 25 member 3 (SLC25A3) to modulate ATP production. We further generated a transgenic knockin mouse model of CYTB-187AA silencing and found that reduction of CYTB-187AA impairs females' fertility by decreasing the number of ovarian follicles. For the first time, we uncovered the novel mPACT pattern of a mitochondrial mRNA and demonstrated the physiological function of this 14 protein encoded by mtDNA.
线粒体基因组转录 13 种 mRNA,这些 mRNA 编码对氧化磷酸化至关重要的知名蛋白质。我们在这里证明,细胞色素 b(CYTB)是复合物 III 中唯一的线粒体 DNA 编码转录本,也使用细胞质核糖体的标准遗传密码而不是线粒体遗传密码编码一个未被识别的 187 个氨基酸长的蛋白质,CYTB-187AA。在用质谱和抗体验证了这种源于细胞质翻译的 mtDNA 编码蛋白(mPACT)的存在后,我们表明 CYTB-187AA 主要定位于线粒体基质中,并通过与溶质载体家族 25 成员 3(SLC25A3)相互作用来调节 ATP 产生,从而促进原始到幼稚过渡中的多能状态。我们进一步生成了一个 CYTB-187AA 沉默的转基因敲入小鼠模型,发现降低 CYTB-187AA 会通过减少卵巢滤泡的数量来降低雌性的生育能力。我们首次揭示了一种线粒体 mRNA 的新 mPACT 模式,并证明了这种由 mtDNA 编码的 14 种蛋白质的生理功能。
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