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Molecular functions of MCM8 and MCM9 and their associated pathologies

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ISCIENCE
卷 26, 期 6, 页码 -

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CELL PRESS
DOI: 10.1016/j.isci.2023.106737

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MCM8 and MCM9 are recently discovered minichromosome maintenance proteins that play roles in various DNA-related processes and diseases, including DNA replication, meiosis, homologous recombination, and mismatch repair. Variants of MCM8/MCM9 may predispose carriers to infertility and cancer and should be included in relevant diagnostic testing.
Minichromosome Maintenance 8 Homologous Recombination Repair Factor (MCM8) and Minichromosome Maintenance 9 Homologous Recombination Repair Factor (MCM9) are recently discovered minichromosome maintenance proteins and are implicated in multiple DNA-related processes and pathologies, including DNA replication (initiation), meiosis, homologous recombination and mismatch repair. Consistent with these molecular functions, variants of MCM8/MCM9 may predispose carriers to disorders such as infertility and cancer and should therefore be included in relevant diagnostic testing. In this overview of the (patho)physiological functions of MCM8 and MCM9 and the phenotype of MCM8/MCM9 variant carriers, we explore the potential clinical implications of MCM8/MCM9 variant carriership and highlight important future directions of MCM8 and MCM9 research. With this review, we hope to contribute to better MCM8/MCM9 variant carrier management and the poten-tial utilization of MCM8 and MCM9 in other facets of scientific research and medical care.

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