Common Postzygotic Mutational Signatures in Healthy Adult Tissues Related to Embryonic Hypoxia
2022
Yaqiang Hong | Dake Zhang | Xiangtian Zhou | Aili Chen | Amir Abliz | Jian Bai | Liang Wang | Qingtao Hu | Kenan Gong | Xiaonan Guan | Mengfei Liu | Xinchang Zheng | Shujuan Lai | Hongzhu Qu | Fuxin Zhao | Shuang Hao | Zhen Wu | Hong Cai | Shaoyan Hu | Yue Ma | Junting Zhang | Yang Ke | Qian-Fei Wang | Wei Chen | Changqing Zeng
Postzygotic mutations are acquired in normal tissues throughout an individual’s lifetime and hold clues for identifying mutagenic factors. Here, we investigated postzygotic mutation spectra of healthy individuals using optimized ultra-deep exome sequencing of the time-series samples from the same volunteer as well as the samples from different individuals. In blood, sperm, and muscle cells, we resolved three common types of mutational signatures. Signatures A and B represent clock-like mutational processes, and the polymorphisms of epigenetic regulation genes influence the proportion of signature B in mutation profiles. Notably, signature C, characterized by C>T transitions at GpCpN sites, tends to be a feature of diverse normal tissues. Mutations of this type are likely to occur early during embryonic development, supported by their relatively high allelic frequencies, presence in multiple tissues, and decrease in occurrence with age. Almost none of the public datasets for tumors feature this signature, except for 19.6% of samples of clear cell renal cell carcinoma with increased activation of the hypoxia-inducible factor 1 (HIF-1) signaling pathway. Moreover, the accumulation of signature C in the mutation profile was accelerated in a human embryonic stem cell line with drug-induced activation of HIF-1α. Thus, embryonic hypoxia may explain this novel signature across multiple normal tissues. Our study suggests that hypoxic condition in an early stage of embryonic development is a crucial factor inducing C>T transitions at GpCpN sites; and individuals’ genetic background may also influence their postzygotic mutation profiles.
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