TY - JOUR
T1 - The fork protection complex promotes parental histone recycling and epigenetic memory
AU - Charlton, Sebastian Jespersen
AU - Flury, Valentin
AU - Kanoh, Yutaka
AU - Genzor, Aitana Victoria
AU - Kollenstart, Leonie
AU - Ao, Wantong
AU - Brøgger, Peter
AU - Weisser, Melanie Bianca
AU - Adamus, Marek
AU - Alcaraz, Nicolas
AU - Delvaux de Fenffe, Charlotte M.
AU - Mattiroli, Francesca
AU - Montoya, Guillermo
AU - Masai, Hisao
AU - Groth, Anja
AU - Thon, Geneviève
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/9
Y1 - 2024/9
N2 - The inheritance of parental histones across the replication fork is thought to mediate epigenetic memory. Here, we reveal that fission yeast Mrc1 (CLASPIN in humans) binds H3-H4 tetramers and operates as a central coordinator of symmetric parental histone inheritance. Mrc1 mutants in a key connector domain disrupted segregation of parental histones to the lagging strand comparable to Mcm2 histone-binding mutants. Both mutants showed clonal and asymmetric loss of H3K9me-mediated gene silencing. AlphaFold predicted co-chaperoning of H3-H4 tetramers by Mrc1 and Mcm2, with the Mrc1 connector domain bridging histone and Mcm2 binding. Biochemical and functional analysis validated this model and revealed a duality in Mrc1 function: disabling histone binding in the connector domain disrupted lagging-strand recycling while another histone-binding mutation impaired leading strand recycling. We propose that Mrc1 toggles histones between the lagging and leading strand recycling pathways, in part by intra-replisome co-chaperoning, to ensure epigenetic transmission to both daughter cells.
AB - The inheritance of parental histones across the replication fork is thought to mediate epigenetic memory. Here, we reveal that fission yeast Mrc1 (CLASPIN in humans) binds H3-H4 tetramers and operates as a central coordinator of symmetric parental histone inheritance. Mrc1 mutants in a key connector domain disrupted segregation of parental histones to the lagging strand comparable to Mcm2 histone-binding mutants. Both mutants showed clonal and asymmetric loss of H3K9me-mediated gene silencing. AlphaFold predicted co-chaperoning of H3-H4 tetramers by Mrc1 and Mcm2, with the Mrc1 connector domain bridging histone and Mcm2 binding. Biochemical and functional analysis validated this model and revealed a duality in Mrc1 function: disabling histone binding in the connector domain disrupted lagging-strand recycling while another histone-binding mutation impaired leading strand recycling. We propose that Mrc1 toggles histones between the lagging and leading strand recycling pathways, in part by intra-replisome co-chaperoning, to ensure epigenetic transmission to both daughter cells.
KW - chromatin replication
KW - Claspin
KW - DNA replication
KW - epigenetic inheritance
KW - epigenome maintenance
KW - fission yeast
KW - H3K9 methylation
KW - heterochromatin
KW - histone chaperone
KW - histone recycling
KW - mouse embryonic stem cells
UR - http://www.scopus.com/inward/record.url?scp=85201712321&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2024.07.017
DO - 10.1016/j.cell.2024.07.017
M3 - Article
C2 - 39094569
AN - SCOPUS:85201712321
SN - 0092-8674
VL - 187
SP - 5029-5047.e21
JO - Cell
JF - Cell
IS - 18
ER -