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Summary Expression Phenotypes Gene Literature (65) GO Terms (19) Nucleotides (1288) Proteins (69) Interactants (422) Wiki
XB-GENEPAGE-5946445

Papers associated with mcm7



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XMCM7, a novel member of the Xenopus MCM family, interacts with XMCM3 and colocalizes with it throughout replication., Romanowski P, Madine MA, Laskey RA., Proc Natl Acad Sci U S A. September 17, 1996; 93 (19): 10189-94.

Identification of two Xenopus laevis genes, xMCM2 and xCDC46, with sequence homology to MCM genes involved in DNA replication., Miyake S, Saito I, Kobayashi H, Yamashita S., Gene. October 10, 1996; 175 (1-2): 71-5.

The RLF-M component of the replication licensing system forms complexes containing all six MCM/P1 polypeptides., Thömmes P, Kubota Y, Takisawa H, Blow JJ., EMBO J. June 2, 1997; 16 (11): 3312-9.

Developmental regulation of MCM replication factors in Xenopus laevis., Sible JC, Erikson E, Hendrickson M, Maller JL, Gautier J., Curr Biol. March 12, 1998; 8 (6): 347-50.

Negative regulation of DNA replication by the retinoblastoma protein is mediated by its association with MCM7., Sterner JM, Dew-Knight S, Musahl C, Kornbluth S, Horowitz JM., Mol Cell Biol. May 1, 1998; 18 (5): 2748-57.

cDNA cloning and expression during development of Drosophila melanogaster MCM3, MCM6 and MCM7., Ohno K, Hirose F, Inoue YH, Takisawa H, Mimura S, Hashimoto Y, Kiyono T, Nishida Y, Matsukage A., Gene. September 14, 1998; 217 (1-2): 177-85.

XCDT1 is required for the assembly of pre-replicative complexes in Xenopus laevis., Maiorano D, Moreau J, Méchali M., Nature. April 6, 2000; 404 (6778): 622-5.

Reconstitution of licensed replication origins on Xenopus sperm nuclei using purified proteins., Gillespie PJ, Li A, Blow JJ., BMC Biochem. January 1, 2001; 2 15.                

The Xenopus Xmus101 protein is required for the recruitment of Cdc45 to origins of DNA replication., Van Hatten RA, Tutter AV, Holway AH, Khederian AM, Walter JC, Michael WM., J Cell Biol. November 25, 2002; 159 (4): 541-7.          

DNA damage-induced replication arrest in Xenopus egg extracts., Stokes MP, Michael WM., J Cell Biol. October 27, 2003; 163 (2): 245-55.                

The role of Cdc6 in ensuring complete genome licensing and S phase checkpoint activation., Oehlmann M, Score AJ, Blow JJ., J Cell Biol. April 26, 2004; 165 (2): 181-90.                  

A Xenopus Dbf4 homolog is required for Cdc7 chromatin binding and DNA replication., Jares P, Luciani MG, Blow JJ., BMC Mol Biol. June 28, 2004; 5 5.          

A requirement for MCM7 and Cdc45 in chromosome unwinding during eukaryotic DNA replication., Pacek M, Walter JC., EMBO J. September 15, 2004; 23 (18): 3667-76.

Functional uncoupling of MCM helicase and DNA polymerase activities activates the ATR-dependent checkpoint., Byun TS, Pacek M, Yee MC, Walter JC, Cimprich KA., Genes Dev. May 1, 2005; 19 (9): 1040-52.

Identification of full genes and proteins of MCM9, a novel, vertebrate-specific member of the MCM2-8 protein family., Lutzmann M, Maiorano D, Méchali M., Gene. December 5, 2005; 362 51-6.

The ATPase activity of MCM2-7 is dispensable for pre-RC assembly but is required for DNA unwinding., Ying CY, Gautier J., EMBO J. December 21, 2005; 24 (24): 4334-44.

Regulation of replication licensing by acetyltransferase Hbo1., Iizuka M, Matsui T, Takisawa H, Smith MM., Mol Cell Biol. February 1, 2006; 26 (3): 1098-108.

Gene expression changes at metamorphosis induced by thyroid hormone in Xenopus laevis tadpoles., Das B, Cai L, Carter MG, Piao YL, Sharov AA, Ko MS, Brown DD., Dev Biol. March 15, 2006; 291 (2): 342-55.        

Excess Mcm2-7 license dormant origins of replication that can be used under conditions of replicative stress., Woodward AM, Göhler T, Luciani MG, Oehlmann M, Ge X, Gartner A, Jackson DA, Blow JJ., J Cell Biol. June 5, 2006; 173 (5): 673-83.              

Differential requirements for MCM proteins in DNA replication in Drosophila S2 cells., Crevel G, Hashimoto R, Vass S, Sherkow J, Yamaguchi M, Heck MM, Cotterill S., PLoS One. September 5, 2007; 2 (9): e833.              

Plx1 is required for chromosomal DNA replication under stressful conditions., Trenz K, Errico A, Costanzo V., EMBO J. March 19, 2008; 27 (6): 876-85.              

Cdc7-Drf1 kinase links chromosome cohesion to the initiation of DNA replication in Xenopus egg extracts., Takahashi TS, Basu A, Bermudez V, Hurwitz J, Walter JC., Genes Dev. July 15, 2008; 22 (14): 1894-905.            

Identification of an arginine-rich motif in human papillomavirus type 1 E1;E4 protein necessary for E4-mediated inhibition of cellular DNA synthesis in vitro and in cells., Roberts S, Kingsbury SR, Stoeber K, Knight GL, Gallimore PH, Williams GH., J Virol. September 1, 2008; 82 (18): 9056-64.

MCM7 interacts with androgen receptor., Shi YK, Yu YP, Zhu ZH, Han YC, Ren B, Nelson JB, Luo JH., Am J Pathol. December 1, 2008; 173 (6): 1758-67.

Replication initiation complex formation in the absence of nuclear function in Xenopus., Krasinska L, Fisher D., Nucleic Acids Res. April 1, 2009; 37 (7): 2238-48.            

Tipin/Tim1/And1 protein complex promotes Pol alpha chromatin binding and sister chromatid cohesion., Errico A, Cosentino C, Rivera T, Losada A, Schwob E, Hunt T, Costanzo V., EMBO J. December 2, 2009; 28 (23): 3681-92.              

GEMC1 is a TopBP1-interacting protein required for chromosomal DNA replication., Balestrini A, Cosentino C, Errico A, Garner E, Costanzo V., Nat Cell Biol. May 1, 2010; 12 (5): 484-91.        

Interaction of human MCM2-7 proteins with TIM, TIPIN and Rb., Numata Y, Ishihara S, Hasegawa N, Nozaki N, Ishimi Y., J Biochem. June 1, 2010; 147 (6): 917-27.

G2 phase chromatin lacks determinants of replication timing., Lu J, Li F, Murphy CS, Davidson MW, Gilbert DM., J Cell Biol. June 14, 2010; 189 (6): 967-80.                

MCM-BP regulates unloading of the MCM2-7 helicase in late S phase., Nishiyama A, Frappier L, Méchali M., Genes Dev. January 15, 2011; 25 (2): 165-75.

Roles of histone chaperone CIA/Asf1 in nascent DNA elongation during nucleosome replication., Ishikawa K, Ohsumi T, Tada S, Natsume R, Kundu LR, Nozaki N, Senda T, Enomoto T, Horikoshi M, Seki M., Genes Cells. October 1, 2011; 16 (10): 1050-62.  

Mcm8 and Mcm9 form a dimeric complex in Xenopus laevis egg extract that is not essential for DNA replication initiation., Gambus A, Blow JJ., Cell Cycle. April 15, 2013; 12 (8): 1225-32.                

The dimeric Mcm8-9 complex of Xenopus laevis likely has a conserved function for resistance to DNA damage., Kanemaki MT., Cell Cycle. May 1, 2013; 12 (9): 1338-9.  

DNA polymerase κ-dependent DNA synthesis at stalled replication forks is important for CHK1 activation., Bétous R, Pillaire MJ, Pierini L, van der Laan S, Recolin B, Ohl-Séguy E, Guo C, Niimi N, Grúz P, Nohmi T, Friedberg E, Cazaux C, Maiorano D, Hoffmann JS., EMBO J. July 31, 2013; 32 (15): 2172-85.                

DNA topoisomerase IIα controls replication origin cluster licensing and firing time in Xenopus egg extracts., Gaggioli V, Le Viet B, Germe T, Hyrien O., Nucleic Acids Res. August 1, 2013; 41 (15): 7313-31.                

Quantitative proteomics of Xenopus laevis embryos: expression kinetics of nearly 4000 proteins during early development., Sun L, Bertke MM, Champion MM, Zhu G, Huber PW, Dovichi NJ., Sci Rep. February 26, 2014; 4 4365.                              

NCOA4 transcriptional coactivator inhibits activation of DNA replication origins., Bellelli R, Castellone MD, Guida T, Limongello R, Dathan NA, Merolla F, Cirafici AM, Affuso A, Masai H, Costanzo V, Grieco D, Fusco A, Santoro M, Carlomagno F., Mol Cell. July 3, 2014; 55 (1): 123-37.

Polyubiquitylation drives replisome disassembly at the termination of DNA replication., Moreno SP, Bailey R, Campion N, Herron S, Gambus A., Science. October 24, 2014; 346 (6208): 477-81.

Closing the MCM cycle at replication termination sites., Lengronne A, Pasero P., EMBO Rep. December 1, 2014; 15 (12): 1226-7.

Protein phosphatase 2A and Cdc7 kinase regulate the DNA unwinding element-binding protein in replication initiation., Gao Y, Yao J, Poudel S, Romer E, Abu-Niaaj L, Leffak M., J Biol Chem. December 26, 2014; 289 (52): 35987-6000.

Termination of DNA replication forks: "Breaking up is hard to do"., Bailey R, Priego Moreno S, Gambus A., Nucleus. January 1, 2015; 6 (3): 187-96.      

DNA interstrand cross-link repair requires replication-fork convergence., Zhang J, Dewar JM, Budzowska M, Motnenko A, Cohn MA, Walter JC., Nat Struct Mol Biol. March 1, 2015; 22 (3): 242-7.      

The mechanism of DNA replication termination in vertebrates., Dewar JM, Budzowska M, Walter JC., Nature. September 17, 2015; 525 (7569): 345-50.                            

Structure of human Cdc45 and implications for CMG helicase function., Simon AC, Sannino V, Costanzo V, Pellegrini L., Nat Commun. May 18, 2016; 7 11638.                

Xenopus Mcm10 is a CDK-substrate required for replication fork stability., Chadha GS, Gambus A, Gillespie PJ, Blow JJ., Cell Cycle. August 17, 2016; 15 (16): 2183-2195.            

p97 Promotes a Conserved Mechanism of Helicase Unloading during DNA Cross-Link Repair., Fullbright G, Rycenga HB, Gruber JD, Long DT., Mol Cell Biol. November 14, 2016; 36 (23): 2983-2994.

CRL2Lrr1 promotes unloading of the vertebrate replisome from chromatin during replication termination., Dewar JM, Low E, Mann M, Räschle M, Walter JC., Genes Dev. February 1, 2017; 31 (3): 275-290.

Reversal of DDK-Mediated MCM Phosphorylation by Rif1-PP1 Regulates Replication Initiation and Replisome Stability Independently of ATR/Chk1., Alver RC, Chadha GS, Gillespie PJ, Blow JJ., Cell Rep. March 7, 2017; 18 (10): 2508-2520.                

CUL-2LRR-1 and UBXN-3 drive replisome disassembly during DNA replication termination and mitosis., Sonneville R, Moreno SP, Knebel A, Johnson C, Hastie CJ, Gartner A, Gambus A, Labib K., Nat Cell Biol. May 1, 2017; 19 (5): 468-479.            

An intact Mcm10 coiled-coil interaction surface is important for origin melting, helicase assembly and the recruitment of Pol-α to Mcm2-7., Perez-Arnaiz P, Bruck I, Colbert MK, Kaplan DL., Nucleic Acids Res. July 7, 2017; 45 (12): 7261-7275.                

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