Accession PRJCA021017
Title The mechanism and function of H3K79 methylation in regulating transcription elongation rate
Relevance Epigenetic
Data types Transcriptome or Gene expression
Raw sequence reads
Genome sequencing
Organisms Homo sapiens
Description This study used mass spectrometry technology to systematically identify the recognition proteins of H3K79 modification, used ChIP-seq to analyze the molecular mechanism by which H3K79 methylation regulates transcription elongation rate, and used transcriptome sequencing to analyze the impact of blocked transcription elongation on RNA processing.Finally, we focused on the impact of H3K79 methylation on host cell transcription under viral infection.
Sample scope Monoisolate
Release date 2024-06-11
Publication
PubMed ID Article title Journal name DOI Year
38905100 DOT1L/H3K79me2 represses HIV-1 reactivation via recruiting DCAF1 Cell Reports 10.1016/j.celrep.2024.114368 2024
Grants
Agency program Grant ID Grant title
National Natural Science Foundation of China (NSFC) 31970619
National Natural Science Foundation of China (NSFC) 32171289
National Key Research and DevelopmentProgram of China 2021YFA1100500
Submitter Liang    Chen  (liang_chen@whu.edu.cn)
Organization Wuhan University
Submission date 2023-11-03

Project Data

Resource name Description
BioSample (12)  show -