Distinct features of ribonucleotides within genomic DNA in Aicardi-Goutières syndrome (AGS)-ortholog mutants of Saccharomyces cerevisiae .
Deepali L KundnaniTaehwan YangAlli L GombolayKuntal MukherjeeGary NewnamChance MeersZeel H MehtaCeline MouawadFrancesca StoriciPublished in: bioRxiv : the preprint server for biology (2023)
Ribonucleoside monophosphates (rNMPs) are abundantly found within genomic DNA of cells. The embedded rNMPs alter DNA properties and impact genome stability. Mutations in ribonuclease (RNase) H2, a key enzyme for rNMP removal, are associated with the Aicardi-Goutières syndrome (AGS), a severe neurological disorder. Here, we engineered two AGS-ortholog mutations in Saccharomyces cerevisiae : rnh201 -G42S and rnh203 -K46W. Using the ribose-seq technique and the Ribose-Map bioinformatics toolkit, we unveiled rNMP abundance, composition, hotspots, and sequence context in these yeast AGS-ortholog mutants. We found higher rNMP incorporation in the nuclear genome of rnh201 -G42S than in wild-type and rnh203- K46W-mutant cells, and an elevated rCMP content in both mutants. Moreover, we uncovered unique rNMP patterns in each mutant, highlighting a differential activity of the AGS mutants towards rNMPs embedded on the leading or on the lagging strand of DNA replication. This study guides future research on rNMP characteristics in human genomic samples carrying AGS mutations.
Keyphrases
- wild type
- saccharomyces cerevisiae
- induced apoptosis
- circulating tumor
- cell free
- cell cycle arrest
- single molecule
- copy number
- genome wide
- endothelial cells
- case report
- nucleic acid
- endoplasmic reticulum stress
- cell death
- signaling pathway
- gene expression
- single cell
- brain injury
- cell proliferation
- pi k akt
- current status
- induced pluripotent stem cells
- cerebral ischemia