晩発効果研究部門 DNA損傷シグナル研究部門
Bibliograpy
最近の日本語総説を紹介しておきます。
ファンコニ貧血の新規原因遺伝子RFWD3の同定とその機能解析 高田 穰 医学の歩み TOPICS266(6/7): 545-546 2018
稲野将二郎、髙田 穰 ファンコニ貧血の新規原因遺伝子RFWD3/FANCWの機能解析から明らかになった相同組換え反応制御機構 生化学 90巻第3号 pp.371-380 (2018)
Fanconi貧血 - DNAクロスリンク損傷修復の分子機構から臨床まで- 平明日香、稲野将二郎、高田 穣 遺伝子医学MOOK別冊 シリーズ:最新遺伝医学研究と遺伝カウンセリング シリーズ1 「最新遺伝性腫瘍・家族性腫瘍研究と遺伝カウンセリング」 〔編集:三木義男先生〕
家族性腫瘍学 —家族性腫瘍の最新研究動向— II.各論 原因遺伝子 Fanconi anemia 経路によるDNA鎖間結合の修復メカニズム 稲野将二郎、平明日香、高田 穣 日本臨床 73間 増刊号6 305−310項
ゲノムを司るインターメア 非コードDNAの新たな展開 小林武彦編 化学同人 11章 「ゲノム脆弱部位の維持と機能」 高田 穣
2019年
Regulation of R-loops and genome instability in Fanconi anemia. Yusuke Okamoto, James Hejna, Minoru Takata J Biochemistry Tokyo (in press) 2019
A prospctive cohort study to define the clinical features and outcome of lung cancers harboring HER2 aberration (HER2-CS STUDY) in Japan” Ninomiya, Kiichiro; Hata, Tae; Yoshioka, Hiroshige; Ohashi, Kadoaki; Bessho, Akihiro; Hosokawa, Shinobu; Ishikawa, Nobuhisa; Yamasaki, Masahiro; Shibayama, Takuo; Aoe, Keisuke; Kozuki, Toshiyuki; Harita, Shingo; Ueda, Yutaka; Murakami, Toshi; Fujimoto, Nobukazu; Yanai, Hiroyuki ; Toyooka, Shinichi; Takata, Minoru; Hotta, Katsuyuki; Kiura, Katsuyuki. Chest(in press) 2019
Minako Mori, Asuka Hira, Kenichi Yoshida, Hideki Muramatsu, Yusuke Okuno, Yuichi Shiraishi, Michiko Anmae, Jun Yasuda, Shu Tadaka, Kengo Kinoshita, Tomoo Osumi, Yasushi Noguchi, Souichi Adachi, Ryoji Kobayashi, Hiroshi Kawabata, Kohsuke Imai, Tomohiro Morio, Kazuo Tamura, Akifumi Takaori-Kondo, Masayuki Yamamoto, Satoru Miyano, Seiji Kojima, Etsuro Ito, Seishi Ogawa, Keitaro Matsuo, Hiromasa Yabe, Miharu Yabe, Minoru Takata.Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.Haematologica in press (2019)
2018年
FANCD2 protects genome stability by recruiting RNA processing enzymes to resolve R-loops during mild replication stress. Yusuke Okamoto, Masako Abe, Akiko Itaya, Junya Tomida, Masamichi Ishiai, Akifumi Takaori-Kondo, Masato Taoka, Toshiaki Isobe, and Minoru Takata. FEBS J. 2018 Nov 15. doi: 10.1111/febs.14700.
Miharu Yabe, Takashi Koike, Keisuke Ohtsubo, Eri Imai, Tsuyoshi Morimoto, Hiromitsu Takakura, Katsuyoshi Koh, Kenichi Yoshida, Seishi Ogawa, Etsuro Ito,Yusuke Okuno, Hideki Muramatsu, Seiji Kojima, Keitaro Matsuo, Minako Mori, Asuka Hira, Minoru Takata and Hiromasa Yabe.Associations of complementation group, ALDH2genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia. Ann Hematol. 2018 Oct 27. doi: 10.1007/s00277-018-3517-0.
Warsaw Breakage Syndrome DDX11 helicase acts jointly with RAD17 in the repair of bulky lesions and replication through abasic sites. Takuya Abe (IFOM), Masato Ooka (IFOM), Ryotaro Kawasumi (IFOM), Keiji Miyata (Tokyo Metropolitan University), Minoru Takata (Kyoto University), Kouji Hirota (Tokyo Metropolitan University), Dana Branzei (IFOM). Proc Natl Acad Sci U S A. 2018 Aug 14;115(33):8412-8417. doi: 10.1073/pnas.1803110115. Epub 2018 Jul 30
Histone Methylation by SETD1A Protects Nascent DNA through the Nucleosome Chaperone Activity of FANCD2. Higgs MR, Sato K, Reynolds JJ, Begum S, Bayley R, Goula A, Vernet A, Paquin KL, Skalnik DG, Kobayashi W, Takata M, Howlett NG, Kurumizaka H, Kimura H, Stewart GS. Mol Cell. 2018 Jun 7. pii: S1097-2765(18)30392-7. doi: 10.1016/j.molcel.2018.05.018. [Epub ahead of print] PMID: 29937342
Replication stress induces accumulation of FANCD2 at central region of large fragile genes.Okamoto Y, Iwasaki WM, Kugou K, Takahashi KK, Oda A, Sato K, Kobayashi W, Kawai H, Sakasai R, Takaori-Kondo A, Yamamoto T, Kanemaki MT, Taoka M, Isobe T, Kurumizaka H, Innan H, Ohta K, Ishiai M, Takata M. Nucleic Acids Res. 2018 Apr 6;46(6):2932-2944. doi: 10.1093/nar/gky058. PMID: 29394375
2017年
Selective cytotoxicity of the anti-diabetic drug, metformin, in glucose-deprived chicken DT40 cells.Kadoda K, Moriwaki T, Tsuda M, Sasanuma H, Ishiai M, Takata M, Ide H, Masunaga SI, Takeda S, Tano K. PLoS One. 2017 Sep 19;12(9):e0185141. doi: 10.1371/journal.pone.0185141. eCollection 2017.
Mochizuki AL, Katanaya A, Hayashi E, Hosokawa M, Moribe E, Motegi A, Ishiai M, Takata M, Kondoh G, Watanabe H, Nakatsuji N, Chuma S. PARI regulates stalled replication fork processing to maintain genome stability upon replication stress in mice.Mol Cell Biol. 2017 Sep 11. 37(23). pii: e00117-17.doi: 10.1128/MCB.00117-17.
Biallelic mutations in the ubiquitin ligase RFWD3cause Fanconi anemia. Kerstin Knies, Shojiro Inano, María J. Ramírez, Masamichi Ishiai, Jordi Surallés, Minoru Takata, and Detlev Schindler.J Clin Invest. 2017 Aug 1;127(8):3013-3027. doi: 10.1172/JCI92069. Epub 2017 Jul 10. PMID: 28691929
RFWD3-mediated ubiquitination promotes timely removal of both RPA and RAD51 from DNA damage sites to facilitate homologous recombination. Shojiro Inano, Koichi Sato, Yoko Katsuki, Wataru Kobayashi, Hiroki Tanaka, Kazuhiro Nakajima, Shinichiro Nakada, Hiroyuki Miyoshi, Kerstin Knies, Akifumi Takaori-Kondo, Detlev Schindler, Masamichi Ishiai, Hitoshi Kurumizaka, Minoru Takata. Mol Cell. 2017 Jun 1;66(5):622-634.e8. doi: 10.1016/j.molcel.2017.04.022. PMID: 28575658
Common Variable Immunodeficiency Caused by FANC Mutations.Sekinaka Y, Mitsuiki N, Imai K, Yabe M, Yabe H, Mitsui-Sekinaka K, Honma K, Takagi M, Arai A, Yoshida K, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Muramatsu H, Kojima S, Hira A, Takata M, Ohara O, Ogawa S, Morio T, Nonoyama S.J Clin Immunol. 2017 Jul;37(5):434-444.doi: 10.1007/s10875-017-0396-4. [Epub ahead of print]PMID: 28493158
Mutation Research special section “Protein modifications in DNA repair and cancer” Editorial. Minoru Takata Mutat Res. 2017 Oct;803-805:42. doi: 10.1016/j.mrfmmm.2017.06.001. Epub 2017 Jun 10.
Mutation Research special section “Protein modifications in DNA repair and cancer” Activation of the FA pathway mediated by phosphorylation and ubiquitination.Ishiai M, Sato K, Tomida J, Kitao H, Kurumizaka H, Takata M. Mutat Res. 2017 Oct;803-805:89-95. doi: 10.1016/j.mrfmmm.2017.05.003. Epub 2017 May 5. Review.
2016年
Hideki Muramatsu, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Sayoko Doisaki, Atsushi Narita, Hirotoshi Sakaguchi, Nozomu Kawashima, Xinan Wang, Yinyan Xu, Kenichi Chiba, Hiroko Tanaka, Asahito Hama, Masashi Sanada, Yoshiyuki Takahashi, Hitoshi Kanno, Hiroki Yamaguchi, Shouichi Ohga, Atsushi Manabe, Hideo Harigae, Shinji Kunishima, Eiichi Ishii, Masao Kobayashi, Kenichi Koike, Kenichiro Watanabe, Etsuro Ito, Minoru Takata, Miharu Yabe, Seishi Ogawa, Satoru Miyano, and Seiji Kojima. Clinical Utility of Next-generation Sequencing for Inherited Bone Marrow Failure Syndromes. Genet Med. 2017 Jan 19. doi: 10.1038/gim.2016.197.
Chen Ling, Jing Huang, Zhijiang Yan, Yongjiang Li, Mioko Ohzeki, Masamichi Ishiai, Dongyi Xu, Minoru Takata, Michael Seidman, and Weidong Wang. Bloom syndrome complex promotes FANCM recruitment to stalled replication forks and facilitates both repair and traverse of DNA interstrand crosslinks. Cell Discov. 2016 Dec 20;2:16047. doi: 10.1038/celldisc.2016.47. PMID: 28058110
Tian X, Patel K, Ridpath JR, Chen Y, Zhou YH, Neo D, Clement J, Takata M, Takeda S, Sale J, Wright FA, Swenberg JA, Nakamura J. Homologous recombination and translesion DNA synthesis play critical roles on tolerating DNA damage caused by trace levels of hexavalent chromium. pLOSOne 2016 Dec 1;11(12):e0167503.
Sato K, Shimomuki M, Katsuki Y, Takahashi D, Kobayashi W, Ishiai M, Miyoshi H, Takata M, Kurumizaka H. FANCI-FANCD2 stabilizes the RAD51-DNA complex by binding RAD51 and protects the 5′-DNA end. Nucleic Acids Res. 2016 Sep 30. pii: gkw876.PMID: 27694619
Katsuki Y, Takata M. Defects in HR repair behind the human diseases: FA and HBOC. Endocr Relat Cancer. 2016 Oct;23(10):T19-37.
Yabe M, Yabe H, Morimoto T, Fukumura A, Ohtsubo K, Koike T, Yoshida K, Ogawa S, Ito E, Okuno Y, Muramatsu H, Kojima S, Matsuo K, Hira A, Takata M. The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype. Br J Haematol. 2016 Nov;175(3):457-461. doi: 10.1111/bjh.14243.
2015年
Masamichi Ishiai, Junya Tomida, Akiko Itaya, James Hejna, Minoru Takata. The Fanconi Anemia Pathway and Interstrand Cross-Link Repair. DNA Replication, Recombination, and Repair. pp 175-210. Edited by Fumio Hanaoka and Kaoru Sugasawa. Springer Japan.
Takahashi D, Sato K, Hirayama E, Takata M, Kurumizaka H. Human FAN1 promotes strand incision in 5′-flapped DNA complexed with RPA. J Biochem. 2015 Apr 27. 158(3):263-70.
Suzuki NM, Niwa A, Yabe M, Hira A, Okada C, Amano N, Watanabe A, Watanabe K, Heike T, Takata M, Nakahata T, Saito MK. Pluripotent cell models of fanconi anemia identify the early pathological defect in human hemoangiogenic progenitors. Stem Cells Transl Med. 2015 Apr;4(4):333-8.
Hira A, Yoshida K, Sato K, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Shimamoto A, Tahara H, Ito E, Kojima S, Kurumizaka H, Ogawa S, Takata M, Yabe H, Yabe M. Mutations in the Gene Encoding the E2 Conjugating Enzyme UBE2T Cause Fanconi Anemia. Am J Hum Genet. 2015 Jun 4;96(6):1001-7. doi: 10.1016/j.ajhg.2015.04.022.
2014年
Defective FANCI Binding by a Fanconi Anemia-Related FANCD2 Mutant. Sato K, Ishiai M, Takata M, Kurumizaka H. PLoS One. 2014 Dec 9;9(12):e114752. doi: 10.1371/journal.pone.0114752. eCollection 2014.
The Trp53-Trp53inp1-Tnfrsf10b Pathway Regulates the Radiation Response of Mouse Spermatogonial Stem Cells. Kei Ishii, Masamichi Ishiai, Hiroko Morimoto, Mito Kanatsu-Shinohara, Ohtsura Niwa, Minoru Takata, and Takashi Shinohara. Stem Cell Reports. 2014 Oct 14;3(4):676-89. doi: 10.1016/j.stemcr.2014.08.006. Epub 2014 Sep 18.
Expression and purification of human FANCI and FANCD2 using Escherichia coli cells. Takahashi D, Sato K, Shimomuki M, Takata M, Kurumizaka H. Protein Expr Purif. 2014 Aug 26;103C:8-15.
Modularized functions of the Fanconi anemia core complex. Huang Y, Leung JW, Lowery M, Matsushita N, Wang Y, Shen X, Huong D, Takata M, Chen J, Li L. Cell Rep. 2014 Jun 26;7(6):1849-57. doi: 10.1016/j.celrep.2014.04.029. Epub 2014 Jun 5.
FANCD2 binds CtIP and regulates DNA-end resection during DNA interstrand crosslink repair. Unno J, Itaya A, Taoka M, Sato K, Tomida J, Sakai W, Sugasawa K, Ishiai M, Ikura T, Isobe T, Kurumizaka H, Takata M. Cell Rep. 2014 May 22;7(4):1039-47. doi: 10.1016/j.celrep.2014.04.005. Epub 2014 May 1.
Tumor suppressor RecQL5 controls recombination induced by DNA crosslinking agents. Hosono Y, Abe T, Ishiai M, Islam MN, Arakawa H, Wang W, Takeda S, Ishii Y, Takata M, Seki M, Enomoto T. Biochim Biophys Acta. 2014 May;1843(5):1002-12. doi: 10.1016/j.bbamcr.2014.01.005. Epub 2014 Jan 10.
2013年
- A novel interplay between the Fanconi anemia core complex and ATR-ATRIP kinase during DNA cross-link repair.
- Tomida J, Itaya A, Shigechi T, Unno J,Uchida E, Ikura M, Masuda Y, Matsuda S, Adachi J, Kobayashi M, Meetei AR, Maehara Y, Yamamoto Kl, Kamiya K, Matsuura A, Matsuda T, Ikura T, Ishiai M, Tkata M.
Nucleic Acids Res.2013 Aug 1;41(14):6930-6941.
- Synergistic Effect of Olaparib with Combination of Cisplatin on PTEN-Deficient Lung Cancer Cells.
- Minami D, Takigawa N, Takeda H, Takata M, Ochi N, Ichihara E, Hisamoto A, Hotta K, Tanimoto M, Kiura K.
Mol Cancer Res.2013 Feb;11(2):140-8.
- NBS1 directly activates ATR independently of MRE11 and TOPBP1
- Kobayashi M, Hayashi N, Tkata M, Yamamoto K.
Genes Cells.2013 Mar;18(3):238-46
2012年
- DNA robustly stimulates FANCD2 monoubiquitylation in the complex with FANCI.
- Sato K, Toda K, Ishiai M, Takata M, Kurumizaka H.
Nucleic Acids Res.2012 May 1;40(10):4553-61.
- Matched sibling donor stem cell transplantation for Fanconi anemia patients with T-cell somatic mosaicism.
- Yabe M, Shimizu T, Morimoto T, Koike T, Takakura H, Tsukamoto H, Muroi K, Oshima K, Asami K, Takata M, Yamashita T, Kato S, Yabe H.
Pediatr Transplant.2012 Jun;16(4):340-5.
- Histone chaperone activity of Fanconi anemia proteins, FANCD2 and FANCI, is required for DNA crosslink repair.
- Sato K, Ishiai M, Toda K, Furukoshi S, Osakabe A, Tachiwana H, Takizawa Y, Kagawa W, Kitao H, Dohmae N, Obuse C, Kimura H, Takata M, Kurumizaka H.
EMBO J.2012 Jul 24;31(17):3524-36.
- Mcm8 and Mcm9 Form a Complex that Functions in Homologous Recombination Repair Induced by DNA Interstrand Crosslinks.
- Nishimura K, Ishiai M, Horikawa K, Fukagawa T, Takata M, Takisawa H, Kanemaki MT.
Mol Cell.2012 Aug 24;47(4):511-22.
- A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network.
- Yan Z, Guo R, Paramasivam M, Shen W, Ling C, Fox D 3rd, Wang Y, Oostra AB, Kuehl J, Lee DY, Takata M, Hoatlin ME, Schindler D, Joenje H, de Winter JP, Li L, Seidman MM, Wang W.
Mol Cell.2012 Jul 13;47(1):61-75.
- Establishment of the DNA repair-defective mutants in DT40 cells.
- Ishiai M, Uchida E, and Takata M.
Methods Mol Biol.2012;920:39-49.
- ATR-Chk1 signaling pathway and homologous recombinational repair protect cells from 5-fuluorouracil cytotoxicity.
- Fujinaka Y, Matsuoka K, Iimori M, Tuul M, Sakasai R, Yoshinaga K, Saeki H, Morita M, Kakeji Y, Gillespie DA, Yamamoto Kl, Takata M, Kitao H, Maehara Y.
DNA Repair (Amst).2012 Mar 1;11(3):247-58.
- ATR-ATRIP kinase complex triggers activation of the Fanconi anemia DNA repair pathway.
- Tomoko Shigechi, Junya Tomida, Koichi Sato, Masahiko Kobayashi, John K.Eykelenboom, Fabio Pessina, Yanbin Zhang, Emi Uchida, Masamichi Ishiai, Noel F.Lowndes, Kenichi Yamamoto, Hitoshi Kurumizaka, Yoshihiko Maehara, and Minoru Tanaka.
Cancer Research(in press)
2011年
- Establishment of the DNA repair-defective mutants in DT40 cells.
- Ishiai M, Uchida E, and Takata M.
Methods Mol Biol(in press)
- Cell autonomous essential requirement for formaldehyde catabolism in the absence of the Fanconi Anaemia DNA repair pathway.
- Rosado IV, Langevin F, Crossan GP, Takata M, and Patel KJ.
Nat Struc and Mol Biol(in press)
- Predisposition to cancer caused by genetic and functional defects of Mammalian atad5.
- Bell DW, Sikdar N, Takata M(35名中30番目), Myung K.
PLoS Genet. 2011 Aug;7(8):e1002245.
- Evaluation of Homologous Recombinational Repair in Chicken B Lymphoma Cell Line, DT40.
- Kitao H, Hirano S, Takata M.
Methods Mol Biol.2011;745:293-309.
- Direct Inhibition of TNF-α Promoter Activity by Fanconi Anemia Protein FANCD2.
- Matsushita N, Endo Y, Sato K, Kurumizaka H, Yamashita T, Takata M, Yanagi S.
PLoS One.2011;6(8):e23324.
- USP1 deubiquitinase maintains phosphorylated CHK1 by limiting its DDB1-dependent degradation.
- Guervilly JH, Renaud E, Takata M, Rosselli F.
Hum Mol Genet.2011 Jun 1;20(11):2171-81.
- The role of SNM1 family nucleases in etoposide-induced apoptosis.
- Hosono Y, Abe T, Ishiai M, Takata M, Enomoto T, Seki M.
Biochem Biopys Res Commun.2011 Jul 8;410(3):568-73.
- Fanconi anemia: a disorder defective in the DNA damege response.
- Kitao H, Tkata M.
Int J Hematol.2011 Apr;93(4):417-24.
- Guest editorial:fanconi anemia and the DNA damage response.
- Takata M.
Int J Hematol. 2011 Apr;93(4):415-6.
- FancJ/Brip1 helicase protects ageinst genomic losses and gains in vertebrate cells.
- Kitao H, Nanda I, Sugino RP, Kinomura A, Yamazoe M, Arakawa H, Schmid M, Innan H, Hiom K, Takata M.
Genes to Cells 2011 Jun;16(6):714-27
- The involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway.
- Yamamoto KY, Kobayashi S, Kurumizaka H, Takata M, Kono K, Jiricny J, Takeda S, Hirota K.
Proc.Natl.Acad. Sci. USA. 2011 Apr 19;108(16):6492-6.
2010年
- KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents.
- Yoshikiyo K, Kratz K, Hirota K, Nishihara K, Takata M, Kurumizaka H, Horimoto S, Takeda S, Jiricny J.
Proc. Natl. Acad. Sci. USA. 2010 Dec 14;107(50):21553-7.
2009年
- The Fanconi anemia pathway: Insights from somatic cell genetics using DT40 cell line.
- Takata M., Ishiai M, ando Kitao H.
Invited review. Mutat.Res.668:92-102(2009)
2008年
- FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway.
- Ishiai M, Kitao H, Smogorzewska A, Tomida J, Kinomura A, Uchida E, Saberi A, Kinoshita E, Kinoshita-Kikuta E, Koike T, Tashiro S, Elledge SJ, & Takata M.
Nat Struct Mol Biol.2008 Nov;15(11):1138-46.
- KU70/80, DNA-PKcs, and Artemis are essential for the rapid induction of apoptosis after massive DSB formation.
- Abe T, Ishiai M, Hosono Y, Yoshimura A, Tada S, Adachi N, Koyama H, Takata M, Takeda S, Enomoto T, Seki M.
Cell Signal.2008 Nov;20(11):1978-85.Epub 2008 Jul 10.
- Regulation of histone H4 acetylation by transcription factor E2A in lg gene conversion.
- Kitao H, Kimura M, Yamamoto K, Seo H, Namikoshi K, Agata Y, Ohta K, Takata M.
Int lmmunol. 2008 Feb;20(2):277-84.Epub 2008 Jan 7.
- FANCG promotes formation of a newly identified protein complex containing BRCA2,FANCD2 and XRCC3.
- Wilson JB, Yamamoto K, Marriott AS, Hussain S, Sung P, Hoatlin ME, Mathew CG, Takata M, Thompson LH, Kupfer GM, Jones NJ.
Onocogene.2008 Jun 12;27(26):3641-52. Epub 2008 Jan 21.
- Induction of lung adenocarcinoma in transgenic mice expressing activated EGFR driven by the SP-C promoter.
- Ohashi K, Rai K, Fujiwara Y, Osawa M, Hirano S, Takata K, Kondo E, Yoshino T, Takata M, Tanimoto M, Kiura K.
Cancer Sci.2008 Jun 16.
2007年
- Arequirement of FancL and FancD2 monoubiquitination in DNA repair.
- Seki S, Ohzeki M, Uchida A, Hirano S, Matsushita N, Kitao H, Oda T, Yamashita T, Kashihara N, Tsubahara A, Takata M, Ishiai M.
Genes Cells. 2007 Mar;12(3):299-310.
- Characterizaiton of the short isoform of Helios overexpressed in patients with T-cell malignancies.
- Tabayashi T, Ishimaru F, Takata M, Kataoka I, Nakase K, Kozuka T, Tanimoto M.
Cancer Sci. 2007 Feb;98(2):182-8.
- Activation of douwnstream epidermal growth factor receptor(EGFR)signaling provides gefitinib-resistance in cells carrying EGFR mutation.
- Uchida A, Hirano S, Kitao H, Ogino A, Rai K, Toyooka S, Takigawa N, Tabata M, Takata M, Kiura K, Tanimoto M.
Cancer Sci.2007 Mar;98(3):357-63.
- FAAP100 is essential for activation of the Fanconi anemia-assosiated DNA damage response pathway.
- Ling C, Ishiai M, Ali AM, Medhurst AL, Neveling K, Kalb R, Yan Z, Xue Y, Oostra AB, Auerbach AD, Hoatlin ME, Schindler D, Joenje H, de Winter JP, Takata M, Meetei AR, Wang W.
EMBO J.2007 Apr 18;26(8):2104-14.
- The effect of gefitinib on B-RAF mutant non-small cell lung cancer and transfectants.
- Toyooka S, Uchida A, Shigematsu H, Soh J, Ogino A, Takata M, Kiura K, Ouchida M, Kosaka T, Aoe M, Mitsudomi T, Date H.
J Thorac Oncol. 2007 Apr;2(4):321-4.
- Emergence of Epidermal Growth Factor Receptor T790M Mutation during Chronic Exposure to Gefitinib in a Non Small Cell Lung Cancer Cell Line.
- Ogino A, Kitao H, Hirano S, Uchida A, Ishiai M, Kozuki T, Takigawa N, Takata M, Kiura K, Tanimoto M.
Cancer Res. 2007 Aug 15;67(16):7807-14.
- Epidermal growth factor receptor mutation status and adjuvant chemotherapy with uracil-tagafur for adenocarcinoma of the lung.
- Suehisa H, Toyooka S, Hotta K, Uchida A, Soh J, Fujiwara Y, Matsuo K, Ouchida M, Takata M, Kiura K, Date H.
J Clin Oncol. 2007 Sep 1;25(25):3952-7.
- Subcellular distribution of human RDM1 protein isoforms and their nucleolar accumulation in response to heat shock and proteotoxic stress.
- Messaoudi L, Yang YG, Kinomura A, Stavreva DA, Yan G, Bortolin-Cavaille ML, Arakawa H, Buerstedde JM, Hainaut P, Cavaille J, Takata M, Van Dyck E.
Nucleic Acids Res. 2007 Oct 1;35(19):6571-6587. Epub 2007 Sep 28.
- Cells deficient in the FANC/BRCA pathway are hypersensitive to plasma levels of formaldehyde.
- Ridpath JR, Nakamura A, Tano K, Luke AM, Sonoda E, Arakawa H, Buerstedde JM, Gillespie DA, Sale JE, Yamazoe M, Bishop D,Takata M, Takeda S, Watanabe M, Swenberg JA, Nakamura J.
Cancer Res. 2007 Dec 1;67(23):11117-22.
- Deubiquitination of FANCD2 Is Required for DNA Crosslink Repair.
- Oestergaard VH, Langevin F, Kuiken HJ, Pace P, Niedzwiedz W, Simpson LJ, Ohzeki M, Takata M, Sale JE, Patel KJ.
Mol Cell. 2007 Dec 14;28(5):798-809.
2006年
- Functional interplay between BRCA2/FANCD1 and FANCC in DNA repair.
- Kitao H, Yamamoto K, Matsushita N, Ohzeki M, Ishiai M, Takata M.
J Biol Chem.2006 Jul 28;281(30); 21312-20.
- 53BP1 contributes to survival of cells irradiated with X-ray during G1 without Ku70 or Artemis.
- Iwabuchi K, Hashimoto M, Matsui T, Kurihara T, Shimizu H, Adachi N, Ishiai M, Yamamoto K, Tauchi H, Takata M, Koyama H, Date T.
Genes Cells.2006 Aug;11(8):935-48
2005年
- Similar Effects of Brca2 Truncation and Rad51 Paralog Deficiency on Immunoglobulin V Gene Diversification in DT40 Cells Support an Early Role for Rad51 Paralogs in Homologous Recombination.
- Hatanaka A, Yamazoe M, Sale JE, Takata M, Yamamoto K, Kitao H, Sonoda E, Kikuchi K, Yonetani Y, Takeda S.
Mol Cell Biol. 2005 Feb;25(3):1124-34.
- Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLM.
- Hirano S, Yamamoto K, Ishiai M, Yamazoe M, Seki M, Matsushita N, Ohzeki M, Yamashita YM, Arakawa H, Buerstedde JM, Enomoto T, Takeda S, Thompson LH, Takata M.
EMBO J. 2005 Jan 26;24(2):418-27. Epub 2004 Dec 23.
- RDM1, a Novel RNA-recognition motif(RRM)-containing protein involved in the cell response to cisplatin in vertebrates.
- Hamimes S, Arakawa H, Stasiak AZ, Kierzek AM, Hirano S, Yang YG, Takata M, Stasiak A, Buerstedde JM, Van Dyck E.
J Biol Chem. 2005 Mar 11;280(10):9225-9235.
- Fanconi anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination.
- Yamamoto K, Hirano S, Ishiai M, Morishima K, Kitao H, Namikoshi K, Kimura M, Matsushita N, Arakawa H, Buerstedde JM, Komatsu K, Thompson LH, Takata M.
Mol Cell Biol. 2005 Jan;25(1)34-43.51.
- Role of NAD dependent deacetylases SIRT1 and SIRT2 in radiation- and cisplatin-induced cell death in vertebrate cells.
- Matsushita N, Takami Y, Kimura M, Tachiiri S, Ishiai M, Nakayama T, Takata M.
Genes Cells. 2005 Apr;10(4):321-32.
- A FancD2-Monoubiquitin Fusion Reveals Hidden Functions of Fanconi Anemia Core Complex in DNA Repair.
- Matsushita N, Kitao H, Ishiai M, Nagashima N, Hirano S, Okawa K, Ohta T, Yu DS, McHugh PJ, Hickson ID, Venkitaraman AR, Kurumizaka H, Takata M.
Mol Cell.2005 Sep 16;19(6):841-7.
- Multiple repair pathways mediate tolerance to chemotherapeutic cross-linking agents in vertebrate cells.
- Nojima K, Hochegger H, Saberi A, Fukushima T, Kikuchi K, Yoshimura M, Orelli BJ, Bishop DK, Hirano S, Ohzeki M, Ishiai M, Yamamoto K, Takata M, Arakawa H, Buerstedde JM, Yamazoe M, Kawamoto T, Araki K, Takahashi JA, Hashimoto N, Takeda S, Sonoda E.
Cancer Res. 2005 Dec 15;65(24):11704-11.
2004年
- Recombination repair pathway in the maintenance of chromosomal integrity against DNA interstrand crosslinks.
- Sasaki MS, Takta M, Sonoda E, Tachibana A, Takeda S.
Cytogenet Genome Res.2004;104(1-4):28-34.
- DNA crosslink repair protein SNM1A interacts with PIAS1 in nuclear focus formation.
- M Ishiai, M Kimura, K Namikoshi, M Yamozoe, K Yamamoto, H Arakawa, K Agematsu, N Matsushita, S Takeda, J-M. Buerstedde and M Takata.(2004)
Mol Cell Biol 2004 Dec;24(24):10733-41.
2003年
- Fanconi anemia FANCG protein in mitigating radiation- and enzyme-induced DNA double-strand breaks by homologous recombination in vertebrate cells.
- Yamamoto K, Ishiai M, Matsushita N, Arakawa H, Lamerdine JE, Buerstedde J-M, Tanimoto M, Harada M, Thompson LH, Takata M.
Mol Cell Biol 23; 5421-5430, 2003
- Over-expression of the dominant-negative isoform of lkaros confers resistance to dexamethasone-induced and anti-lgM-induced apoptosis.
- Sezaki N, Ishimaru F, Takata M, Tabayashi T, Nakase K, Kozuka T, Fujii K, Nakayama H, Teshima T, Harada M, Tanimoto M.
Br J Haematol. 121:165-9,2003
- Multiple roles of Rev3, the catalytic subnit of polzeta in maintaining genome stability in vertebrates.
- Sonoda E, Okada T, Zhao GY, Tateishi S, Araki K, Yamaizumi M, Yagi T, Verkaik NS, van Gent DC, Takata M, Takeda S.
EMBO J. 2003 Jun 16;22(12):3188-3197.
- DNA-PK: the major taeget for wortmannin-mediated radiosensitization by the inhibition of DSB repair via NHEJ pathway.
- Hashimoto M, Rao S, Tokuno O, Yamamoto K, Takata M, Takeda S, Utsumi H.
J Radiat Res(Tokyo).2003 Jun;44(2):151-9.
2002年
- Conserved domains in the chicken homologue of BRCA2.
- Takata M, Tachiiri S, Fujimori A, Thompson LH, Miki Y, Hiraoka M, Takeda S, Yamazoe M.
Oncogene. 21;1130-1134, 2002
- Effects of double-strand break repair proteins on vertebrate telomere structure.
- Wei C, Skopp R, Takata M, Takeda S, Price CM.
Nucleic Acids Res. 30;2862-2870, 2002
- Nbs1 is essential for DNA repair by homologous recombination in higher vertebrate cells.
- Tauchi H, Kobayashi J, Morishima K, van Gent DC, Shiraishi T, Verkaik NS, vanHeems D, Ito E, Nakamura A, Sonoda E, Takata M, Takeda S, Matsuura S, Komatsu K.
Nature. 420;93-98, 2002
- Involvement of vertebrate polkappa in Rad18-independent postreplication repair of UV damage.
- Okada T, Sonoda E, Yamashita YM, Koyoshi S, Tateishi S, Yamaizumi M, Takata M, Ogawa O, Takeda S.
J Biol Chem. 277;48690-48695, 2002
2001年
- Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs.
- Takata M, Sasaki S M, Tachiiri S, Fukushima T, Sonoda E, Schild D, Thompson L H, Takeda S.
Mol Cell Biol 21;2858-2866, 2001
- Homologous-pairing activity of the human DNA-repair proteins, Xrcc3/Rad51C.
- Kurumizaka H, Ikawa S, Nakada M, Eda K, Kagawa W, Takata M, Takeda S, Yokoyama S, Shibata T.
Proc Natl Acad Sci U S A 98;5538-5543, 2001
- Requirement for repair of DNA double-strand breaks by homologous recombination in split-dose recovery.
- Utsumi H, Tano K, TakataM, Takeda S, Elkind MM.
Radiation Research 155;680-686, 2001
- Antisense oligodeoxynucleotides to latent membrane protein 1 induce growth lymphoblastoid cells, but not in EBV-positive natural killer cell lymphoma cells.
- Nogushi T, Ikeda K, Yamamoto K, Yoshida I, Ashiba A, Tsuchiyama J, Shinagawa K, Yoshino T, Takata M, Harada M.
Br J Haematol. 114;84-92, 2001
- Efficient rejoining of radiation-induced DNA double-strand breaks in vertebrate cells deficient in genes of the RAD52 epistasis group.
- Wang H, Zeng ZC, Bui TA, Sonoda E, Takata M, Takeda S, Iliakis G.
Oncogene.20; 2212-2224, 2001
- Ablation of XRCC2/3 transforms immunoglobulin V gene conversion into somatic hypermutation.
- Sale JE, Daniella M.Calandrini DM, Takata M, Takeda S and Neuberger MS.
Nature. 412; 921-926, 2001
- Rad52 partially substitutes for the Rad51 paralog XRCC3 in maintaining chromosomal integrity in vertebrate cells.
- Akira Fujimori, Seiji Tachiiri, Eiichiro Sonoda, Larry H.Thompson, Pawan Kumar Dhar, Masahiro Hiraoka, Shunichi Takeda, Yong Zhang, Michael Rethm And Minoru Takata.
EMBO J. 20; 5513-5520, 2001
- Genetic analysis of the DNA-dependent protein kinase reveals an inhibitory role of Ku in late S-G2 phase DNA double-strand break repair.
- Fukushima T, Takata M, Morrison C, Araki R, Fujimori A, Abe M, Tatsumi K, Jasin M, Dhar PK, Sonoda E,Chiba T, Takeda S.
J Biol Chem. 276;44413-44418, 2001
2000年
- The Rad51 Paralog Rad51B Promotes Homologous Recombinational Repair.
- Takata M, Sasaki M S, Sonoda E, Fukushima T, Morrison C, Albala J, Swagemakers S M A, Kannar R, Thompson L H, Takeda S.
Mol Cell Biol 20; 6476-6482, 2000
- SHP-1/ITIM-independent inhibitory signaling through murine NK cell receptor Ly-49A in a transfected B cell line.
- Motoda K, Takata M, Kiura K, Nakamura I, Harada M.
Immunology 100; 370-377, 2000