bioRxivMolecular BiologyPreprint
Human ribomes reveal DNA-embedded ribonucleotides as a new type of epigenetic mark
Deepali L. KundnaniiD, Taehwan YangiD, Tejasvi ChannagiriiD, Penghao XuiD, Yeunsoo Lee, Mo SuniD, Francisco Martinez-Figueroa, Supreet Randhawa, Ashlesha GogateiD, Youngkyu JeoniD, Stefania MarsiliiD, Gary P. NewnamiD, Yilin LuiD, Vivian S. Park, Sijia Tao, Justin A. LingiD, Raymond F. SchinaziiD, Zachary F. PurselliD, Abdulmelik MohammediD, Patricia Lynn OpreskoiD, Bret FreudenthaliD, Baek KimiD, Soojin V. YiiD, Nataša JonoskaiD, Francesca StoriciiD
Abstract
Ribonucleoside monophosphates (rNMPs) are abundant in DNA, but their distribution and function in human nuclear genomes remain unknown. Here, we mapped nearly one million rNMPs per genome across diverse human cell types, defining a nuclear "ribome" with non-random distribution patterns. rNMPs are enriched in C/G-rich sequences, epigenetically marked regions, and telomeres. Conserved ribonucleotide-enriched zones (REZs) overlap with CpG islands and R-loops. rNMP concentration near transcription start sites (TSSs) correlates positively with gene expression. Wild-type cells display a broader gene-expression range than ribonuclease H2A (RNH2A) knockouts, in which loss of rNMP cleavage causes pronounced retention of embedded rG and strand-biased rC near TSSs, both increasing with gene expression. These findings establish DNA-embedded rNMPs as a novel epigenetic mark that modulates human gene expression.
- organism: human
- assay: DNA methylation
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: statistical model
- Citations
- 1
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