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脆性位点与染色体不稳定性:顺二氨基二氯铂(II)在范可尼贫血淋巴细胞培养物中诱导的断裂分布

Fragile sites and chromosome instability: the distribution of breaks induced by cis-diamine-dichloro-platinum (II) in Fanconi anemia lymphocyte cultures.

作者信息

Porfirio B, Smeets D, Beckers L, Caporossi D, Tedeschi B, Vernole P, Joenje H, Nicoletti B, Dallapiccola B

机构信息

Department of Public Health and Cell Biology, 2nd University of Rome, Italy.

出版信息

Hum Genet. 1991 Jan;86(3):256-60. doi: 10.1007/BF00202404.

DOI:10.1007/BF00202404
PMID:1997377
Abstract

The distribution of chromosome breaks induced by the antitumor drug cis-diamine-dichloroplatinum (II) in lymphocyte cultures from Fanconi anemia patients was analyzed. Breakpoints occurred nonrandomly over an arbitrarily defined human karyotype of 319 bands. These bands were classified according to either their banding pattern or their fragile site status (whether or not a fragile site of a given type is located at a chromosomal band). A significant involvement of G-light and fragile site bands was detected. The preferential occurrence of breaks at fragile site bands was limited to common fragile site bands (essentially of the aphidicolin-type).

摘要

分析了抗肿瘤药物顺二氯二氨铂(II)在范可尼贫血患者淋巴细胞培养物中诱导的染色体断裂分布情况。断点在任意定义的319条带的人类核型上非随机出现。这些带根据其带型或其脆性位点状态(给定类型的脆性位点是否位于染色体带上)进行分类。检测到G浅带和脆性位点带显著受累。脆性位点带处断裂的优先发生仅限于常见脆性位点带(主要是阿非科林型)。

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1
Fragile sites and chromosome instability: the distribution of breaks induced by cis-diamine-dichloro-platinum (II) in Fanconi anemia lymphocyte cultures.脆性位点与染色体不稳定性:顺二氨基二氯铂(II)在范可尼贫血淋巴细胞培养物中诱导的断裂分布
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2
The distribution of MspI-induced breaks in human lymphocyte chromosomes and its relationship to common fragile sites.人淋巴细胞染色体中MspI诱导断裂的分布及其与常见脆性位点的关系。
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Rev3, the catalytic subunit of Polζ, is required for maintaining fragile site stability in human cells.Rev3,Polζ 的催化亚基,是维持人类细胞脆性位点稳定性所必需的。
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Molecular pathogenesis and clinical management of Fanconi anemia.范可尼贫血的分子发病机制与临床管理。

本文引用的文献

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An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature.人类细胞遗传学命名国际系统——高分辨率显带(1981年)。《国际人类细胞遗传学命名法(1981年)》。人类细胞遗传学命名常务委员会报告。
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Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemia.抗肿瘤铂化合物对范可尼贫血的细胞遗传学毒性。
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The FANC pathway and BLM collaborate during mitosis to prevent micro-nucleation and chromosome abnormalities.范可尼贫血(FANC)通路与布卢姆综合征蛋白(BLM)在有丝分裂过程中协同作用,以防止微核形成和染色体异常。
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Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3.范可尼贫血互补组D基因定位于3号染色体p25.3区的一个200千碱基对区域。
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基因决定的染色体不稳定综合征。
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Fragile sites and cancer breakpoints.脆性位点与癌症断点
Cancer Genet Cytogenet. 1984 Jun;12(2):179-81. doi: 10.1016/0165-4608(84)90132-8.
5
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.阿非科林对DNA聚合酶α的抑制作用会在人类染色体的常见脆性位点诱导缺口和断裂。
Hum Genet. 1984;67(2):136-42. doi: 10.1007/BF00272988.
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Nonrandom distribution of chromosome breaks in Fanconi's anemia.范科尼贫血中染色体断裂的非随机分布。
Cytogenet Cell Genet. 1973;12(6):423-34. doi: 10.1159/000130485.
7
Interstrand cross-links and sequence specificity in the reaction of cis-dichloro(ethylenediamine)platinum(II) with DNA.顺式二氯(乙二胺)铂(II)与DNA反应中的链间交联和序列特异性
Biochemistry. 1985 Sep 10;24(19):5027-32. doi: 10.1021/bi00340a011.
8
Differential sensitivity of Fanconi anaemia lymphocytes to the clastogenic action of cis-diamminedichloroplatinum (II) and trans-diamminedichloroplatinum (II).范科尼贫血淋巴细胞对顺二氯二氨铂(II)和反二氯二氨铂(II)致断裂作用的差异敏感性。
Hum Genet. 1985;71(3):206-10. doi: 10.1007/BF00284574.
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The effect of aphidicolin on Fanconi's anemia lymphocyte chromosomes.阿非科林对范科尼贫血淋巴细胞染色体的影响。
Mutat Res. 1985 Dec;144(4):257-63. doi: 10.1016/0165-7992(85)90061-2.
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Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites.
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