Monoubiquitinated H2B, a Main Chromatin Target of Formaldehyde, Is Important for S‐Phase Checkpoint Signaling and Genome Stability

Abstract

ABSTRACTFormaldehyde (FA) is a human carcinogen with ubiquitous environmental exposures and significant endogenous formation. Genotoxic activity of FA stems from its reactivity with DNA‐NH2 groups. Histone lysines are another source of aldehyde‐reactive amino groups in chromatin, however, chromatin/histone damage responses to FA and their biological significance are poorly understood. We examined histone posttranslational modifications in FA‐treated human lung cells and found that the majority of the most prominent small lysine modifications associated with active or inactive chromatin were unchanged. FA moderately decreased H3K9 and H3K27 acetylation and H2A‐K119 monoubiquitination but caused surprisingly severe losses of H2B‐K120 monoubiquitination, especially in primary and stem‐like cells. H2Aub1 decreases reflected its slower ubiquitination linked to a lower ubiquitin availability due to K48‐polyubiquitination of FA‐damaged proteins. Depletion of H2Bub1 resulted from its rapid deubiquitination in part by ATXN7L3‐associated deubiquitinases and was independent on DNA damage signaling, indicating a direct chromatin damage response. Manipulations of H2Bub1 abundance showed that it was important for robust ATM and ATR signaling, efficient S‐phase checkpoint, and suppression of mitotic transmission of unreplicated DNA and formation of micronuclei. Our findings identified H2B deubiquitination as a major FA‐induced chromatin damage response that regulates S‐phase checkpoint signaling and genome stability.