ORCID: https://orcid.org/0009-0004-8635-0657 und Rentmeister, Andrea
ORCID: https://orcid.org/0000-0002-3107-4147
(24. February 2025):
Quantification of Propargylated RNA Nucleosides After Metabolic Labeling Via the Methylation Pathway.
In: ChemBioChem, Vol. 26, No. 7, e202400986
[PDF, 1MB]
Abstract
RNA modifications are involved in numerous biological processes and vary in different cell types. Methylation is the most widespread type of RNA modification and occurs via S-adenosyl-L-methionine (SAM). We recently developed a metabolic labeling approach based on intracellular formation of a clickable SAM analog (SeAdoYn) and demonstrated its use in mapping methyltransferase (MTase) target sites in mRNA from HeLa cells. Here we investigate how metabolic labeling via the clickable SAM analog modifies four different nucleosides in RNA of HEK293T in comparison to HeLa cells. We find that HEK293T cells retain higher cell viability upon feeding the clickable metabolic SAM precursor. In poly(A)+ RNA we find high Aprop/A levels (0.04 %) and in total RNA (but not poly(A)+ RNA) we detect prop3C, which had not been detected previously in HeLa cells. We discuss the findings in the context of data from the literature with respect to mRNA half-lives in cancer and non-cancer cell lines and suggest that CMTr2 is most likely responsible for the high Aprop level in poly(A)+ RNA.
| Item Type: | Journal article |
|---|---|
| Faculties: | Chemistry and Pharmacy > Department of Chemistry |
| Subjects: | 500 Science > 540 Chemistry |
| URN: | urn:nbn:de:bvb:19-epub-128972-9 |
| ISSN: | 1439-4227 |
| Language: | English |
| Item ID: | 128972 |
| Date Deposited: | 28. Oct 2025 14:48 |
| Last Modified: | 28. Oct 2025 14:48 |
| DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 510974120 |
