Zehong Wu

ORCID: 0000-0003-4063-6583
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About
Contact & Profiles
Research Areas
  • RNA modifications and cancer
  • Cancer-related gene regulation
  • RNA and protein synthesis mechanisms
  • Cancer-related molecular mechanisms research
  • HVDC Systems and Fault Protection
  • Viral-associated cancers and disorders
  • RNA Research and Splicing

Sun Yat-sen University
2021-2025

Abstract Serine/arginine-rich splicing factor 7 (SRSF7), a known factor, has been revealed to play oncogenic roles in multiple cancers. However, the mechanisms underlying its have not well addressed. Here, based on N 6-methyladenosine (m 6 A) co-methylation network analysis across diverse cell lines, we find that gene expression of SRSF7 is positively correlated with glioblastoma (GBM) cell-specific m6A methylation. We then indicate novel regulator, which specifically facilitates methylation...

10.1016/j.gpb.2021.11.001 article EN cc-by-nc-nd Genomics Proteomics & Bioinformatics 2021-12-23

ABSTRACT Although plenty of machine learning models have been developed to detect m 6 A RNA modification sites using the electric current signals ONT direct sequencing (DRS) reads, landscape on different isoforms is still a mystery due their limited capacity distinguish individual long reads and isoforms. The primary challenge in training model with single-read accuracy difficulty obtaining data from DRS that comprehensively represent endogenous RNAs. Here, we endogenously label methylated...

10.1101/2024.01.30.577990 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-01-31

ABSTRACT Various genome-wide and transcriptome-wide technologies are based on antibodies, however, the specificity of antibodies different targets has not been characterized or considered in analyses. The antibody-based MeRIP-seq is most widely used method to determine locations N6-methyladenosine (m 6 A) RNAs, especially for differential m A However, antibody specificities RNA regions their resulting technical biases analyses have evaluated. Here, we evaluated using 100 pairs spike-in RNAs...

10.1101/2024.02.04.578119 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-02-05

Abstract Serine/Arginine-Rich Splicing Factor 7 (SRSF7), which is previously recognized as a splicing factor, has been revealed to play oncogenic roles in multiple cancers. However, the mechanisms underlying its have not well addressed. Here, based on N6-methyladenosine (m 6 A) co-methylation network analysis across diverse cell lines, we found SRSF7 positively correlated with glioblastoma cell-specific m A methylation. We then proved novel regulator that specifically facilitates methylation...

10.1101/2021.10.11.463901 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2021-10-11
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