AI Article Synopsis

  • - In fission yeast, the protein Mrc1 is essential for transferring parental histones H3 and H4 to the lagging strand of newly synthesized DNA, ensuring the proper inheritance of epigenetic traits.
  • - Mrc1 helps Mcm2 and DNA polymerase alpha, two important proteins that bind histones, to interact and optimize the parental histone transfer process.
  • - Interestingly, Mrc1's role in histone transfer and epigenetic memory is separate from its traditional functions in DNA replication and checkpoint activation, indicating a complex mechanism underlying epigenetic inheritance.

Article Abstract

Chromatin-based epigenetic memory relies on the symmetric distribution of parental histones to newly synthesized daughter DNA strands, aided by histone chaperones within the DNA replication machinery. However, the mechanism of parental histone transfer remains elusive. Here, we reveal that in fission yeast, the replisome protein Mrc1 plays a crucial role in promoting the transfer of parental histone H3-H4 to the lagging strand, ensuring proper heterochromatin inheritance. In addition, Mrc1 facilitates the interaction between Mcm2 and DNA polymerase alpha, two histone-binding proteins critical for parental histone transfer. Furthermore, Mrc1's involvement in parental histone transfer and epigenetic inheritance is independent of its known functions in DNA replication checkpoint activation and replisome speed control. Instead, Mrc1 interacts with Mcm2 outside of its histone-binding region, creating a physical barrier to separate parental histone transfer pathways. These findings unveil Mrc1 as a key player within the replisome, coordinating parental histone segregation to regulate epigenetic inheritance.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11414769PMC
http://dx.doi.org/10.1016/j.molcel.2024.07.002DOI Listing

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