Yingliang Sheng

ORCID: 0009-0007-0680-2636
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About
Contact & Profiles
Research Areas
  • CRISPR and Genetic Engineering
  • Genomics and Chromatin Dynamics
  • Epigenetics and DNA Methylation
  • Pluripotent Stem Cells Research
  • DNA Repair Mechanisms
  • Hippo pathway signaling and YAP/TAZ
  • Chromosomal and Genetic Variations
  • Genetic Mapping and Diversity in Plants and Animals
  • Plant nutrient uptake and metabolism
  • PARP inhibition in cancer therapy

First Affiliated Hospital of Guangzhou Medical University
2023-2025

State Key Laboratory of Respiratory Disease
2022-2025

Guangzhou Medical University
2022-2025

University of Science and Technology of China
2022-2025

Guangzhou Institutes of Biomedicine and Health
2022-2025

Center for Excellence in Molecular Cell Science
2022-2023

Chinese Academy of Sciences
2022-2023

University of Hong Kong
2022

Guangzhou Regenerative Medicine and Health Guangdong Laboratory
2022

CTCF mediates chromatin insulation and long-distance enhancer-promoter (EP) interactions; however, little is known about how these regulatory functions are partitioned among target genes in key biological processes. Here, we show that Ctcf expression progressively increased during induced pluripotency. In this process, first as a insulator responsible for direct silencing of the somatic gene program and, interestingly, elevated next ensures accessibility contributes to EP interactions...

10.1016/j.celrep.2022.110626 article EN cc-by-nc-nd Cell Reports 2022-04-01

Abstract Although extended pluripotent stem cells (EPSCs) have the potential to form both embryonic and extraembryonic lineages, how their transcriptional regulatory mechanism differs from that of (ESCs) remains unclear. Here, we discovered YY1 binds specific open chromatin regions in EPSCs. Yy1 depletion EPSCs leads a gene expression pattern more similar ESCs than control Moreover, triggers series epigenetic crosstalk activities, including changes DNA methylation, histone modifications...

10.1093/nar/gkac230 article EN cc-by-nc Nucleic Acids Research 2022-03-27

R-loops are prevalent triplex nucleic strands found across various organisms, involved in numerous biological processes. However, the physiological and pathological functions of remain largely unknown due to a lack effective high-resolution detection methods. Here, using nuclease P1, T5 exonuclease, lambda exonuclease mediated digestion ssRNA, ssDNA, dsDNA while preserving RNA:DNA hybrid, we report method named R-loop identification assisted by high-throughput sequencing (RIAN-seq) for...

10.1101/2025.02.21.639597 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2025-02-27

Abstract Cellular totipotency is critical for whole-organism generation, yet how established remains poorly illustrated. Abundant transposable elements (TEs) are activated in totipotent cells, which embryonic totipotency. Here, we show that the histone chaperone RBBP4, but not its homolog RBBP7, indispensable maintaining identity of mouse stem cells (mESCs). Auxin-induced degradation reprograms mESCs to 2C-like cells. Also, loss RBBP4 enhances transition from trophoblast Mechanistically,...

10.1093/nar/gkad219 article EN cc-by Nucleic Acids Research 2023-04-06

Abstract The transition of mouse embryonic stem cells (ESCs) between serum/LIF and 2i(MEK GSK3 kinase inhibitor)/LIF culture conditions serves as a valuable model for exploring the mechanisms underlying ground confused pluripotent states. Regulatory networks comprising core ancillary pluripotency factors drive gene expression programs defining stable naïve pluripotency. In our study, we systematically screened essential ESC pluripotency, identifying TEAD2 an factor maintaining ground-state...

10.1038/s44318-024-00086-5 article EN cc-by The EMBO Journal 2024-04-11
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