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MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM.

Singh TR, Saro D, Ali AM, Zheng XF, Du CH, Killen MW, Sachpatzidis A, Wahengbam K, Pierce AJ, Xiong Y, Sung P, Meetei AR.

Mol Cell. 2010 Mar 26;37(6):879-86. doi: 10.1016/j.molcel.2010.01.036.


The structure of the FANCM-MHF complex reveals physical features for functional assembly.

Tao Y, Jin C, Li X, Qi S, Chu L, Niu L, Yao X, Teng M.

Nat Commun. 2012 Apr 17;3:782. doi: 10.1038/ncomms1779.


Structural peculiarities of the (MHF1-MHF2)4 octamer provide a long DNA binding patch to anchor the MHF-FANCM complex to chromatin: a solution SAXS study.

Wang W, Guo Q, Shtykova EV, Liu G, Xu J, Teng M, Liu P, Dong Y.

FEBS Lett. 2013 Sep 17;587(18):2912-7. doi: 10.1016/j.febslet.2013.07.022. Epub 2013 Jul 22.


Stabilizing and remodeling the blocked DNA replication fork: anchoring FANCM and the Fanconi anemia damage response.

Thompson LH, Jones NJ.

Mol Cell. 2010 Mar 26;37(6):749-51. doi: 10.1016/j.molcel.2010.03.003.


A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability.

Yan Z, Delannoy M, Ling C, Daee D, Osman F, Muniandy PA, Shen X, Oostra AB, Du H, Steltenpool J, Lin T, Schuster B, Décaillet C, Stasiak A, Stasiak AZ, Stone S, Hoatlin ME, Schindler D, Woodcock CL, Joenje H, Sen R, de Winter JP, Li L, Seidman MM, Whitby MC, Myung K, Constantinou A, Wang W.

Mol Cell. 2010 Mar 26;37(6):865-78. doi: 10.1016/j.molcel.2010.01.039.


MHF1 plays Fanconi anaemia complementation group M protein (FANCM)-dependent and FANCM-independent roles in DNA repair and homologous recombination in plants.

Dangel NJ, Knoll A, Puchta H.

Plant J. 2014 Jun;78(5):822-33. doi: 10.1111/tpj.12507. Epub 2014 May 2.


Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway.

Huang M, Kennedy R, Ali AM, Moreau LA, Meetei AR, D'Andrea AD, Chen CC.

DNA Repair (Amst). 2011 Dec 10;10(12):1203-12. doi: 10.1016/j.dnarep.2011.09.006. Epub 2011 Oct 4.


The histone-fold complex MHF is remodeled by FANCM to recognize branched DNA and protect genome stability.

Fox D 3rd, Yan Z, Ling C, Zhao Y, Lee DY, Fukagawa T, Yang W, Wang W.

Cell Res. 2014 May;24(5):560-75. doi: 10.1038/cr.2014.42. Epub 2014 Apr 4.


Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.

Singh TR, Bakker ST, Agarwal S, Jansen M, Grassman E, Godthelp BC, Ali AM, Du CH, Rooimans MA, Fan Q, Wahengbam K, Steltenpool J, Andreassen PR, Williams DA, Joenje H, de Winter JP, Meetei AR.

Blood. 2009 Jul 2;114(1):174-80. doi: 10.1182/blood-2009-02-207811. Epub 2009 May 7.


FANCM and FAAP24 function in ATR-mediated checkpoint signaling independently of the Fanconi anemia core complex.

Collis SJ, Ciccia A, Deans AJ, Horejsí Z, Martin JS, Maslen SL, Skehel JM, Elledge SJ, West SC, Boulton SJ.

Mol Cell. 2008 Nov 7;32(3):313-24. doi: 10.1016/j.molcel.2008.10.014.


Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24.

Kim JM, Kee Y, Gurtan A, D'Andrea AD.

Blood. 2008 May 15;111(10):5215-22. doi: 10.1182/blood-2007-09-113092. Epub 2008 Jan 3.


The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes.

Zhao Q, Saro D, Sachpatzidis A, Singh TR, Schlingman D, Zheng XF, Mack A, Tsai MS, Mochrie S, Regan L, Meetei AR, Sung P, Xiong Y.

Nat Commun. 2014;5:2987. doi: 10.1038/ncomms3987.


FANCM and FAAP24 maintain genome stability via cooperative as well as unique functions.

Wang Y, Leung JW, Jiang Y, Lowery MG, Do H, Vasquez KM, Chen J, Wang W, Li L.

Mol Cell. 2013 Mar 7;49(5):997-1009. doi: 10.1016/j.molcel.2012.12.010. Epub 2013 Jan 17.


The Fanconi anemia protein FANCM is controlled by FANCD2 and the ATR/ATM pathways.

Sobeck A, Stone S, Landais I, de Graaf B, Hoatlin ME.

J Biol Chem. 2009 Sep 18;284(38):25560-8. doi: 10.1074/jbc.M109.007690. Epub 2009 Jul 24.


FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.

Ali AM, Singh TR, Meetei AR.

Mutat Res. 2009 Jul 31;668(1-2):20-6. doi: 10.1016/j.mrfmmm.2009.04.002. Epub 2009 Apr 18. Review.


Differential contribution of the Fanconi anemia-related proteins to repair of several types of DNA damage in cultured silkworm cells.

Sugahara R, Mon H, Lee JM, Shiotsuki T, Kusakabe T.

FEBS Lett. 2014 Nov 3;588(21):3959-63. doi: 10.1016/j.febslet.2014.09.009. Epub 2014 Sep 19.


FANCM of the Fanconi anemia core complex is required for both monoubiquitination and DNA repair.

Xue Y, Li Y, Guo R, Ling C, Wang W.

Hum Mol Genet. 2008 Jun 1;17(11):1641-52. doi: 10.1093/hmg/ddn054. Epub 2008 Feb 19.


A prototypical Fanconi anemia pathway in lower eukaryotes?

McHugh PJ, Ward TA, Chovanec M.

Cell Cycle. 2012 Oct 15;11(20):3739-44. doi: 10.4161/cc.21727. Epub 2012 Aug 16.


FANCM-associated proteins MHF1 and MHF2, but not the other Fanconi anemia factors, limit meiotic crossovers.

Girard C, Crismani W, Froger N, Mazel J, Lemhemdi A, Horlow C, Mercier R.

Nucleic Acids Res. 2014 Aug;42(14):9087-95. doi: 10.1093/nar/gku614. Epub 2014 Jul 18.


A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

Meetei AR, Medhurst AL, Ling C, Xue Y, Singh TR, Bier P, Steltenpool J, Stone S, Dokal I, Mathew CG, Hoatlin M, Joenje H, de Winter JP, Wang W.

Nat Genet. 2005 Sep;37(9):958-63. Epub 2005 Aug 21.

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