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1
Characterization of a protein recognizing minor groove binders-damaged DNA.一种识别小沟结合剂损伤DNA的蛋白质的特性分析。
Nucleic Acids Res. 1996 Nov 1;24(21):4227-33. doi: 10.1093/nar/24.21.4227.
2
DNA minor groove binding agents interfere with topoisomerase II mediated lesions induced by epipodophyllotoxin derivative VM-26 and acridine derivative m-AMSA in nuclei from L1210 cells.DNA小沟结合剂可干扰由表鬼臼毒素衍生物VM - 26和吖啶衍生物m - AMSA在L1210细胞核中诱导的拓扑异构酶II介导的损伤。
Biochemistry. 1989 May 2;28(9):3850-5. doi: 10.1021/bi00435a034.
3
The effects of a benzoic acid mustard derivative of distamycin A (FCE 24517) and related minor groove-binding distamycin analogues on the activity of major groove-binding alkylating agents.双氢链霉素A的苯甲酸芥子衍生物(FCE 24517)及相关的小沟结合双氢链霉素类似物对大沟结合烷化剂活性的影响。
Biochem Pharmacol. 1993 Feb 9;45(3):619-26. doi: 10.1016/0006-2952(93)90135-j.
4
Effects of minor groove binding drugs on camptothecin-induced DNA lesions in L1210 nuclei.小沟结合药物对喜树碱诱导的L1210细胞核DNA损伤的影响。
Biochem Pharmacol. 1990 Feb 15;39(4):707-14. doi: 10.1016/0006-2952(90)90149-f.
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Involvement of DNA topoisomerase II in the selective resistance of a mammalian cell mutant to DNA minor groove ligands: ligand-induced DNA-protein crosslinking and responses to topoisomerase poisons.DNA拓扑异构酶II参与哺乳动物细胞突变体对DNA小沟配体的选择性抗性:配体诱导的DNA-蛋白质交联及对拓扑异构酶毒物的反应
Carcinogenesis. 1990 Apr;11(4):659-65. doi: 10.1093/carcin/11.4.659.
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Enhancement and alteration of bleomycin-catalyzed site-specific DNA cleavage by distamycin A and some minor groove binders.Distamycin A及一些小沟结合剂对博来霉素催化的位点特异性DNA切割的增强和改变作用。
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8
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10
Design, synthesis, DNA sequence preferential alkylation and biological evaluation of N-mustard derivatives of Hoechst 33258 analogues.
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1
Chemotherapeutic potential of 9-phenyl acridine: biophysical studies on its binding to DNA.9-苯基吖啶的化疗潜力:与 DNA 结合的生物物理研究。
Eur Biophys J. 2010 Jul;39(8):1243-9. doi: 10.1007/s00249-010-0577-z. Epub 2010 Feb 5.
2
Mechanisms of resistance to alkylating agents.烷基化试剂耐药机制。
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本文引用的文献

1
Excision of DNA adducts of nitrogen mustards by bacterial and mammalian 3-methyladenine-DNA glycosylases.细菌和哺乳动物的3-甲基腺嘌呤-DNA糖基化酶对氮芥DNA加合物的切除作用
Carcinogenesis. 1996 Apr;17(4):643-8. doi: 10.1093/carcin/17.4.643.
2
The base excision repair pathway.碱基切除修复途径。
Trends Biochem Sci. 1995 Oct;20(10):391-7. doi: 10.1016/s0968-0004(00)89086-6.
3
DNA topoisomerase I is involved in both repression and activation of transcription.DNA拓扑异构酶I参与转录的抑制和激活过程。
Nature. 1993 Sep 16;365(6443):227-32. doi: 10.1038/365227a0.
4
Nucleotide excision repair. II: From yeast to mammals.核苷酸切除修复。II:从酵母到哺乳动物。
Trends Genet. 1993 Jun;9(6):211-7. doi: 10.1016/0168-9525(93)90121-w.
5
It was a very good year for DNA repair.对DNA修复来说,这是非常不错的一年。
Cell. 1994 Jan 14;76(1):1-4. doi: 10.1016/0092-8674(94)90165-1.
6
Mammalian topoisomerase I has base mismatch nicking activity.哺乳动物拓扑异构酶I具有碱基错配切口活性。
J Biol Chem. 1994 Jun 3;269(22):15498-504.
7
3T3 NIH murine fibroblasts and B78 murine melanoma cells expressing the Escherichia coli N3-methyladenine-DNA glycosylase I do not become resistant to alkylating agents.表达大肠杆菌N3-甲基腺嘌呤-DNA糖基化酶I的3T3 NIH小鼠成纤维细胞和B78小鼠黑色素瘤细胞不会对烷基化剂产生抗性。
Carcinogenesis. 1994 Mar;15(3):533-7. doi: 10.1093/carcin/15.3.533.
8
DNA sequence-specific adenine alkylation by the novel antitumor drug tallimustine (FCE 24517), a benzoyl nitrogen mustard derivative of distamycin.新型抗肿瘤药物他林莫司汀(FCE 24517,一种偏端霉素的苯甲酰氮芥衍生物)引起的DNA序列特异性腺嘌呤烷基化。
Nucleic Acids Res. 1995 Jan 11;23(1):81-7. doi: 10.1093/nar/23.1.81.
9
Distamycin A and tallimustine inhibit TBP binding and basal in vitro transcription.放线菌素A和他利莫司汀抑制TBP结合及体外基础转录。
Nucleic Acids Res. 1995 May 25;23(10):1657-63. doi: 10.1093/nar/23.10.1657.
10
Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei.从分离的哺乳动物细胞核的可溶性提取物中,RNA聚合酶II进行准确的转录起始。
Nucleic Acids Res. 1983 Mar 11;11(5):1475-89. doi: 10.1093/nar/11.5.1475.

一种识别小沟结合剂损伤DNA的蛋白质的特性分析。

Characterization of a protein recognizing minor groove binders-damaged DNA.

作者信息

Colella G, Bonfanti M, D'Incalci M, Broggini M

机构信息

Molecular Pharmacology Unit, LCP, Department of Oncology, Istituto di Richerche Farmacologiche Mario Negri, Milan, Italy.

出版信息

Nucleic Acids Res. 1996 Nov 1;24(21):4227-33. doi: 10.1093/nar/24.21.4227.

DOI:10.1093/nar/24.21.4227
PMID:8932377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC146256/
Abstract

By using electromobility shift assay (EMSA), we have identified a protein able to recognize the DNA only if it was previously reacted with minor groove binders. This protein binds with very high affinity AT containing DNA treated with minor groove binders such as distamycin A, Hoechst 33258 and 33342, CC-1065 and ethidium bromide minor groove intercalator, but not with major groove binders such as quinacrine mustard, cisplatin or melphalan, or with topoisomerase I inhibitor camptothecin or topoisomerase II inhibitor doxorubicin. This protein was found to be present in different extracts of human, murine and hamster cells, with the human protein which appears to have a molecular weight slightly lower than that of the other species. This protein was found to be expressed both in cancer and normal tissues. By using molecular ultrafiltration techniques as well as southwestern analysis it was estimated that the apparent molecular weight is close to 100 kDa. We can exclude an identity between this protein and other proteins, with a similar molecular weight previously reported to be involved in DNA damage recognition/repair, such as topoisomerase I, mismatch repair activities such as the prokaryotic MutS protein and its human homologue hMSH2 or proteins of the nucleotide excision repair system such as ERCC1, -2, -3 and -4.

摘要

通过使用电泳迁移率变动分析(EMSA),我们鉴定出一种蛋白质,该蛋白质只有在与小沟结合剂预先反应后才能识别DNA。这种蛋白质以非常高的亲和力结合用小沟结合剂处理过的含AT的DNA,如偏端霉素A、Hoechst 33258和33342、CC-1065以及溴化乙锭小沟嵌入剂,但不与大沟结合剂如喹吖因氮芥、顺铂或美法仑结合,也不与拓扑异构酶I抑制剂喜树碱或拓扑异构酶II抑制剂阿霉素结合。发现这种蛋白质存在于人类、小鼠和仓鼠细胞的不同提取物中,其中人类蛋白质的分子量似乎略低于其他物种。发现这种蛋白质在癌症组织和正常组织中均有表达。通过使用分子超滤技术以及蛋白质印迹分析,估计其表观分子量接近100 kDa。我们可以排除该蛋白质与其他蛋白质的同一性,这些蛋白质分子量相似,先前报道参与DNA损伤识别/修复,如拓扑异构酶I、错配修复活性如原核MutS蛋白及其人类同源物hMSH2或核苷酸切除修复系统的蛋白质如ERCC1、-2、-3和-4。