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Chengqi YI

Chengqi YI


Email: chengqi.yi(at)pku(dot)edu(dot)cn;

Telephone: +86-10-62752895;

Lab Homepage: http://www.yi-lab.org/


Research Area: 


We probe the pathways and mechanisms of DNA/RNA modification and de-modification. In order to do so, we integrate multiple disciplines including chemical biology, epigenetics, nucleic acid chemistry, cell biology, biochemistry, genomics, and structural biology. An ultimate goal is to uncover new functions and regulatory mechanisms of the epigenetic DNA/RNA modifications.

1. RNA Modifications and Epitranscriptomics
More than 100 distinct post-transcriptional modifications have been characterized so far; they were considered to be static and unalterable after covalent installation. Recent discoveries of reversible RNA methylation in the form of N6-methyladenosine (m6A) have demonstrated RNA modification-mediated regulation of gene expression, leading to the emerging field of “epitranscriptomics”.
In addition to m6A, there are other epitranscriptomic marks. My laboratory recently discovered that pseudouridine (Ψ) and N1-methyladenosine (m1A), two post-transcriptional modifications in non-coding RNAs, are also present in mammalian mRNAs. My laboratory showed that these epitranscriptomic marks are prevalent in mRNA, dynamically-regulated by various stimuli and reversible by potential “eraser” proteins in the case of m1A. However, the biological consequences of mRNA pseudouridylation and m1A methylation are unknown. Utilizing epitranscriptome sequencing tools we have developed, we hope to elucidate the functional consequences and regulatory mechanisms of these RNA modifications, hence leading to new territories in the nascent field of epitranscriptomics.

2. TET- and TDG-dependent Active DNA Demethylation
The ten-eleven translocation (TET)-dependent generation and removal of oxidized derivatives of 5-methylcytosine (5mC), namely 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC) and 5-carboxylcytosine (5caC), uncovered a new paradigm of active DNA demethylation in mammalian genomes. Besides acting as demethylation intermediates, these oxidized variants of 5mC may also play functional roles. Emerging evidence has suggested 5hmC as a stable epigenetic modification implicated in many biological processes and various diseases. 5fC and 5caC, further oxidation products of 5hmC, accumulate at distal regulatory elements as active DNA demethylation intermediates and can be removed through base excision repair by mammalian thymine DNA glycosylase (TDG). My laboratory recently developed “fC-CET”, a bisulfite-free, base-resolution method for the genome-wide identification of 5fC sites. We will continue to develop robust and sensitive sequencing technologies, including those applicable to single-cell studies and clinical investigations, to dissect the functional roles of these epigenetic DNA modifications.

3. DNA Repair and Protein-DNA Interactions
Aberrant modification to DNA can lead to cytotoxic or mutagenic consequences. Once damaged, cellular DNA must be promptly repaired. Organisms have evolved a variety of mechanisms to repair these cytotoxic or mutagenic damages; in the Yi Group, we are interested in the base-excision repair and direct repair pathways. One component of our research is to utilize a novel chemical cross-linking technique to stabilize protein-DNA interactions in these systems. For instance, my group recently revealed an unprecedented mechanism of DNA repair glycosylase hNEIL1: it promotes tautomerization of thymine glycol—a preferred substrate—for efficient substrate recognition and excision. An integrative approach uniting chemical synthesis, structural biology and biochemical/biophysical characterization is used to study these interactions in DNA/RNA base repair and modification proteins.



Selected Publications:

1. Chenxu Zhu, Lining Lu, Jun Zhang, Zongwei Yue, Jinghui Song, Shuai Zong, Menghao Liu, Olivia Stovicek, Yi Qin Gao, Chegnqi Yi * (2016). Tautomerization-dependent recognition and excision of oxidation damage in base-excision DNA repair. Proc. Natl. Acad. Sci. USA., 113, 7792. (*:Corresponding author)

2. Xiaoyu Li, Xushen Xiong, Kun Wang, Lixia Wang, Xiaoting Shu, Shiqing Ma, Chengqi Yi*. (2016). Transcriptome-wide mapping reveals reversible and dynamic N1-methyladenosine methylome. Nat. Chem. Biol., 12, 311.
3. Bo Xia, Dali Han, Xingyu Lu, Zhaozhu Sun, Ankun Zhou, Qiangzong Yin, Hu Zeng, Menghao Liu, Xiang Jiang, Wei Xie, Chuan He*, Chengqi Yi* (2015). Bisulfite-free and Base-resolution Analysis of 5-formylcytosine at Whole-genome Scale. Nat. Methods, 12(11), 1047.
4. Xiaoyu Li, Ping Zhu, Shiqing Ma, Jinghui Song, Jinyi Bai, Fangfang Sun, Chengqi Yi*. (2015). Chemical Pull-Down Reveals Comprehensive and Dynamic Pseudouridylation in Mammalian Transcriptome. Nat. Chem. Biol., 11(8), 592.
5. John Karijolich J, Chengqi Yi, Yi-Tao Yu*. (2015). Transcriptome-wide Dynamics of RNA Pseudouridylation. Nat. Rev. Mol. Cell Biol., 16(10), 581.
6. Xiaoyu Li, Shiqing Ma, Chengqi Yi* (2015). Pseudouridine Chemical Labelling and Profiling. Methods Enzymol., 560, 247.
7. Chenxu Zhu, Chengqi Yi*. (2014). Switching Demethylation Activities between AlkB Family RNA/DNA Demethylases through Exchange of Active-Site Residues. Angew. Chem. Int. Ed. 53(14), 3659.
8. Chengqi Yi, Guifang Jia, Guanhua Hou, Qing Dai, Wen Zhang, Guanqun Zheng, Xing Jian, Cai-Guang Yang, Qiang Cui, Chuan He. (2010). Iron-Catalysed Oxidation Intermediates Captured in a DNA Repair Dioxygenase. Nature, 468, 330.
9. Cai-Guang Yang#, Chengqi Yi#, Erica Duguid, Christopher Sullivan, Xing Jian, Phoebe Rice, Chuan He. (2008). Crystal structures of DNA/RNA Repair Enzymes AlkB and ABH2 Bound to dsDNA. Nature, 452, 961.


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