Replication stress responses in human lymphocytes change sex-specifically during aging

The varying incidence of aging-related diseases and the gender gap in life expectancy suggest differences in the aging process between the sexes. Yet, little is known about sexspecific differences in genomic instability, a key factor in aging. Here we analyzed DNA damage responses (DDRs) in cycling human peripheral blood lymphocytes (PBL) from female and male donors of different age focusing on replication stress. Transcriptomics revealed striking sex-dependent expression changes in DDR pathways during aging. Particularly, various DDR components, involved in DNA repair and replication fork remodeling were upregulated with age in men. In contrast, functional analysis indicated reduced activity of the Fanconi Anemia pathway in PBL from older women. In line, DNA fiber spreading and PCNA ubiquitination analyses revealed a shift from fork remodeling to faster DNA damage tolerance (DDT) mechanisms in older women, accompanied by an increase in replication stress. While replication dynamics were unaltered and replication stress rather reduced, PBL from older men were highly dependent on PARP activity. In conclusion, our findings revealed sex-specific strategies to cope with replication stress in PBL from older individuals, namely through DDT pathway switching in women and PARP activation in men, differentially contributing to the decline of genomic stability with age. The experiment is an analysis to compare gene expression in peripheral blood lymphocytes (PBLs) based on age (young [18-25 yrs]/ old [>60 yrs]) and sex (male / female). *************************************************************** Raw files for human/patient samples were not submitted to GEO due to concerns about submitting personally identifiable sequence data for open access. ***************************************************************