U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination
    • Showing Current items.

    MCM8 minichromosome maintenance 8 homologous recombination repair factor [ Homo sapiens (human) ]

    Gene ID: 84515, updated on 17-Jun-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    A novel cancer-germline gene DAZL promotes progression and cisplatin resistance of non-small cell lung cancer by upregulating JAK2 and MCM8.

    A novel cancer-germline gene DAZL promotes progression and cisplatin resistance of non-small cell lung cancer by upregulating JAK2 and MCM8.
    Zhou L, Le MNU, Du Y, Chen X, Jin M, Xiang H, Xia LE, Zhou J, He J, Ning Y.

    05/31/2024
    Mechanism of DNA unwinding by MCM8-9 in complex with HROB.

    Mechanism of DNA unwinding by MCM8-9 in complex with HROB.
    Acharya A, Bret H, Huang JW, Mütze M, Göse M, Kissling VM, Seidel R, Ciccia A, Guérois R, Cejka P., Free PMC Article

    05/23/2024
    Activity, substrate preference and structure of the HsMCM8/9 helicase.

    Activity, substrate preference and structure of the HsMCM8/9 helicase.
    McKinzey DR, Li C, Gao Y, Trakselis MA., Free PMC Article

    08/14/2023
    Enhancer-driven transcription of MCM8 by E2F4 promotes ATR pathway activation and glioma stem cell characteristics.

    Enhancer-driven transcription of MCM8 by E2F4 promotes ATR pathway activation and glioma stem cell characteristics.
    Sun YM, Zhang YM, Shi HL, Yang S, Zhao YL, Liu HJ, Li C, Liu HL, Yang JP, Song J, Sun GZ, Yang JK., Free PMC Article

    06/28/2023
    Structural study of the N-terminal domain of human MCM8/9 complex.

    Structural study of the N-terminal domain of human MCM8/9 complex.
    Li J, Yu D, Liu L, Liang H, Ouyang Q, Liu Y.

    03/19/2022
    Associations of MCM8 rs3761873 and rs16991617 variants with abnormal uterine bleeding induced by copper intrauterine device.

    Associations of MCM8 rs3761873 and rs16991617 variants with abnormal uterine bleeding induced by copper intrauterine device.
    Shen Y, Xu L, Zhu W, Zhang Z, Liu J, Jiang L, Liu X, Mao Y, Xu J, Yan X, Sun J, Liu F, Xiong X, Chen X, Che Y, Du J.

    02/5/2022
    Knockdown of MCM8 functions as a strategy to inhibit the development and progression of osteosarcoma through regulating CTGF.

    Knockdown of MCM8 functions as a strategy to inhibit the development and progression of osteosarcoma through regulating CTGF.
    Ren Z, Li J, Zhao S, Qiao Q, Li R., Free PMC Article

    10/16/2021
    Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome.

    Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome.
    Golubicki M, Bonjoch L, Acuña-Ochoa JG, Díaz-Gay M, Muñoz J, Cuatrecasas M, Ocaña T, Iseas S, Mendez G, Cisterna D, Schubert SA, Nielsen M, van Wezel T, Goldberg Y, Pikarsky E, Robbio J, Roca E, Castells A, Balaguer F, Antelo M, Castellví-Bel S., Free PMC Article

    06/5/2021
    Two novel mutations in the MCM8 gene shared by two Chinese siblings with primary ovarian insufficiency and short stature.

    Two novel mutations in the MCM8 gene shared by two Chinese siblings with primary ovarian insufficiency and short stature.
    Wang F, Guo S, Li P., Free PMC Article

    05/29/2021
    Identification of mini-chromosome maintenance 8 as a potential prognostic marker and its effects on proliferation and apoptosis in gastric cancer.

    Identification of mini-chromosome maintenance 8 as a potential prognostic marker and its effects on proliferation and apoptosis in gastric cancer.
    Huang B, Lin M, Lu L, Chen W, Tan J, Zhao J, Cao Z, Zhu X, Lin J., Free PMC Article

    05/15/2021
    Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency.

    Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency.
    Zhang YX, He WB, Xiao WJ, Meng LL, Tan C, Du J, Lu GX, Lin G, Tan YQ., Free PMC Article

    04/3/2021
    A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation.

    A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation.
    Heddar A, Beckers D, Fouquet B, Roland D, Misrahi M.

    02/6/2021
    Crystal structure of the winged-helix domain of MCM8.

    Crystal structure of the winged-helix domain of MCM8.
    Zeng H, Li J, Xu H, Li H, Liu Y.

    11/28/2020
    MCM8IP activates the MCM8-9 helicase to promote DNA synthesis and homologous recombination upon DNA damage.

    MCM8IP activates the MCM8-9 helicase to promote DNA synthesis and homologous recombination upon DNA damage.
    Huang JW, Acharya A, Taglialatela A, Nambiar TS, Cuella-Martin R, Leuzzi G, Hayward SB, Joseph SA, Brunette GJ, Anand R, Soni RK, Clark NL, Bernstein KA, Cejka P, Ciccia A., Free PMC Article

    08/29/2020
    MCM4, MCM5, and MCM8 may have roles in lung adenocarcinoma prognosis with roles in regulating the cell cycle, DNA replication and other multiple biological processes and pathways

    Genome-wide investigation of the clinical significance and prospective molecular mechanism of minichromosome maintenance protein family genes in patients with Lung Adenocarcinoma.
    Liu K, Kang M, Liao X, Wang R., Free PMC Article

    03/14/2020
    Conceptual MCM8-9 inhibitors will be powerful cancer-specific chemosensitizers for platinum compounds.

    Inhibiting the MCM8-9 complex selectively sensitizes cancer cells to cisplatin and olaparib.
    Morii I, Iwabuchi Y, Mori S, Suekuni M, Natsume T, Yoshida K, Sugimoto N, Kanemaki MT, Fujita M., Free PMC Article

    03/9/2019
    Additional support to the view that MCM8 mutations are involved in the primary ovarian insufficiency phenotype.

    New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family.
    Bouali N, Francou B, Bouligand J, Imanci D, Dimassi S, Tosca L, Zaouali M, Mougou S, Young J, Saad A, Guiochon-Mantel A.

    10/14/2017
    stalled replication forks can be restarted in S phase via homologous recombination using MCM8-9 as an alternative replicative helicase.

    Acute inactivation of the replicative helicase in human cells triggers MCM8-9-dependent DNA synthesis.
    Natsume T, Nishimura K, Minocherhomji S, Bhowmick R, Hickson ID, Kanemaki MT., Free PMC Article

    10/7/2017
    study showed that copy number increase and overexpression of MCM8 may play critical roles in human cancer development.

    Oncogenic activity of amplified miniature chromosome maintenance 8 in human malignancies.
    He DM, Ren BG, Liu S, Tan LZ, Cieply K, Tseng G, Yu YP, Luo JH., Free PMC Article

    09/16/2017
    Significant number of potentially damaging and novel variants in MCM8 in primary ovarian insufficiency; multiallelic association with variants in DDR and MCM8-MCM9 interactome genes.

    MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency.
    Desai S, Wood-Trageser M, Matic J, Chipkin J, Jiang H, Bachelot A, Dulon J, Sala C, Barbieri C, Cocca M, Toniolo D, Touraine P, Witchel S, Rajkovic A., Free PMC Article

    07/22/2017
    Novel mutations p. H317L and p. H601R in the MCM8 gene are potentially causative for primary ovarian insufficiency by dysfunctional DNA repair.

    Minichromosome maintenance complex component 8 mutations cause primary ovarian insufficiency.
    Dou X, Guo T, Li G, Zhou L, Qin Y, Chen ZJ.

    06/10/2017
    Suggest role for MCM8 in the pathogenesis of chronic myelogenous leukemia.

    Expression of minichromosome maintenance 8 in chronic myelogenous leukemia.
    Cai L, Zhao K, Yuan X., Free PMC Article

    10/29/2016
    MCM8, a component of the pre-replication complex, is crucial for gonadal development and maintenance in humans-both males and females. These

    Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure.
    Tenenbaum-Rakover Y, Weinberg-Shukron A, Renbaum P, Lobel O, Eideh H, Gulsuner S, Dahary D, Abu-Rayyan A, Kanaan M, Levy-Lahad E, Bercovich D, Zangen D.

    02/27/2016
    An autosomal recessive ovarian failure disorder caused by an MCM8 mutation that manifests with endocrine dysfunction and genomic instability.

    Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.
    AlAsiri S, Basit S, Wood-Trageser MA, Yatsenko SA, Jeffries EP, Surti U, Ketterer DM, Afzal S, Ramzan K, Faiyaz-Ul Haque M, Jiang H, Trakselis MA, Rajkovic A., Free PMC Article

    04/25/2015
    Chromatin immunoprecipitation analysis using human DR-GFP cells demonstrated that MCM8 and MCM9 proteins are rapidly recruited to DNA damage sites and promote RAD51 recruitment.

    The MCM8-MCM9 complex promotes RAD51 recruitment at DNA damage sites to facilitate homologous recombination.
    Park J, Long DT, Lee KY, Abbas T, Shibata E, Negishi M, Luo Y, Schimenti JC, Gambus A, Walter JC, Dutta A., Free PMC Article

    06/15/2013
    firstprevious page of 2 nextlast