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脆性位点表达的遗传决定因素

Genetic determination of fragile-site expression.

作者信息

Smeets D, Arets A

机构信息

Department of Human Genetics, University of Nijmegen, The Netherlands.

出版信息

Am J Hum Genet. 1990 Aug;47(2):196-201.

Abstract

To explore genetic effects on the expression of chromosomal fragile sites in vitro, we studied the expression of common fragile sites (c-fra) in cultured lymphocytes of a human chimera (Chi46,XX/46,XY). Since the two cell lines in the chimera share the same environment in vitro and in vivo on cell culture preceding chromosome analysis, differences in the expression of c-fra must be due to genetic factors. The peripheral lymphocytes were cultured in medium 199 and in medium RPMI 1640 with and without aphidicolin. All lesions were localized after GTG-banding and mapped to the human idiogram. In the cultures with aphidicolin the XX cells showed, at high (0.4 microM) APC levels, a significantly higher expression of c-fra than did the XY cells. This difference between cell lineages was not confined to certain individual c-fra; rather it was seen for practically all of them. Therefore, we conclude that there are genetic factors which influence the propensity of c-fra to be expressed. Whether sex is one of these factors, or perhaps even the most important one, still has to be elucidated.

摘要

为了在体外探索遗传因素对染色体脆性位点表达的影响,我们研究了一名人类嵌合体(Chi46,XX/46,XY)培养淋巴细胞中常见脆性位点(c-fra)的表达。由于嵌合体中的两个细胞系在染色体分析前的体外和体内细胞培养中共享相同的环境,c-fra表达的差异必定归因于遗传因素。外周淋巴细胞在添加和不添加阿非科林的199培养基和RPMI 1640培养基中培养。所有损伤在GTG显带后定位,并绘制到人类染色体模式图上。在添加阿非科林的培养物中,XX细胞在高浓度(0.4 microM)阿非科林水平下,c-fra的表达明显高于XY细胞。细胞系之间的这种差异并不局限于某些特定的c-fra;实际上,几乎所有的c-fra都存在这种差异。因此,我们得出结论,存在影响c-fra表达倾向的遗传因素。性别是否是这些因素之一,甚至是否是最重要的因素,仍有待阐明。

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本文引用的文献

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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.
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Constitutive fragile sites and cancer.组成型脆性位点与癌症
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Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites.
Cytogenet Cell Genet. 1985;40(1-4):490-535. doi: 10.1159/000132181.
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Rare, polymorphic, and common fragile sites: a classification.
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