The fork protection complex promotes parental histone recycling and epigenetic memory

Sebastian Jespersen Charlton; Valentin Flury; Yutaka Kanoh; Aitana Victoria Genzor; Leonie Kollenstart; Wantong Ao; Peter Brøgger; Melanie Bianca Weisser; Marek Adamus; Nicolas Alcaraz; Charlotte M Delvaux de Fenffe; Francesca Mattiroli; Guillermo Montoya; Hisao Masai; Anja Groth; Geneviève Thon

doi:10.1016/j.cell.2024.07.017

The fork protection complex promotes parental histone recycling and epigenetic memory

Sebastian Jespersen Charlton, Valentin Flury, Yutaka Kanoh, Aitana Victoria Genzor, Leonie Kollenstart, Wantong Ao, Peter Brøgger, Melanie Bianca Weisser, Marek Adamus, Nicolas Alcaraz, Charlotte M Delvaux de Fenffe, Francesca Mattiroli, Guillermo Montoya, Hisao Masai, Anja Groth, Geneviève Thon

Hubrecht Institute

Research output: Contribution to journal/periodical › Article › Scientific › peer-review

15 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	5029-5047.e21
Journal	Cell
Volume	187
Issue number	18
DOIs	https://doi.org/10.1016/j.cell.2024.07.017
Publication status	Published - 05 Sept 2024

Keywords

Histones/metabolism
Schizosaccharomyces/metabolism
Epigenesis, Genetic
Schizosaccharomyces pombe Proteins/metabolism
DNA Replication
Cell Cycle Proteins/metabolism
Mutation
Epigenetic Memory

Access to Document

10.1016/j.cell.2024.07.017

Cite this

Charlton, S. J., Flury, V., Kanoh, Y., Genzor, A. V., Kollenstart, L., Ao, W., Brøgger, P., Weisser, M. B., Adamus, M., Alcaraz, N., Delvaux de Fenffe, C. M., Mattiroli, F., Montoya, G., Masai, H., Groth, A., & Thon, G. (2024). The fork protection complex promotes parental histone recycling and epigenetic memory. Cell, 187(18), 5029-5047.e21. https://doi.org/10.1016/j.cell.2024.07.017

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abstract = "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.",

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Charlton, SJ, Flury, V, Kanoh, Y, Genzor, AV, Kollenstart, L, Ao, W, Brøgger, P, Weisser, MB, Adamus, M, Alcaraz, N, Delvaux de Fenffe, CM, Mattiroli, F, Montoya, G, Masai, H, Groth, A & Thon, G 2024, 'The fork protection complex promotes parental histone recycling and epigenetic memory', Cell, vol. 187, no. 18, pp. 5029-5047.e21. https://doi.org/10.1016/j.cell.2024.07.017

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

PY - 2024/9/5

Y1 - 2024/9/5

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 - Histones/metabolism

KW - Schizosaccharomyces/metabolism

KW - Epigenesis, Genetic

KW - Schizosaccharomyces pombe Proteins/metabolism

KW - DNA Replication

KW - Cell Cycle Proteins/metabolism

KW - Mutation

KW - Epigenetic Memory

U2 - 10.1016/j.cell.2024.07.017

DO - 10.1016/j.cell.2024.07.017

M3 - Article

C2 - 39094569

SN - 0092-8674

VL - 187

SP - 5029-5047.e21

JO - Cell

JF - Cell

IS - 18

ER -