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在中期染色体上检测到富含甲基胞嘧啶的DNA新位点。

New sites of methylcytosine-rich DNA detected on metaphase chromosomes.

作者信息

Barbin A, Montpellier C, Kokalj-Vokac N, Gibaud A, Niveleau A, Malfoy B, Dutrillaux B, Bourgeois C A

机构信息

CNRS URA 147, Institut Gustave Roussy, Villejuif, France.

出版信息

Hum Genet. 1994 Dec;94(6):684-92. doi: 10.1007/BF00206964.

Abstract

In situ immunofluorescence detection of antibodies against 5-methylcytosine on metaphase chromosomes prepared by a new procedure allows the display of new 5-methylcytosine-rich sites as compared to previously published methods. In short-term culture lymphocytes, the immunofluorescent signals give a recurrent pattern in which four types of binding sites can be distinguished. Type I sites are the secondary constrictions and a few juxtacentromeric regions, type II sites correspond to T-bands. Both types I and II sites emit a strong fluorescence. Type III sites form an R-band pattern and emit a weaker fluorescence. Type IV sites are the short arms of acrocentrics, they emit strong but polymorphic signals. The results obtained from control experiments suggest that the pattern observed is rather the expression of an uneven distribution of 5-methylcytosine-rich sites than a consequence of the various treatments used. In a lymphoblastoid cell line known to have a reduced 5-methylcytosine content, it was possible to demonstrate a heterogeneous hypomethylation among chromosome structures, principally involving type I sites. The method opens the possibility of studying in situ on chromosomes, regional variations of methylation in pathological conditions.

摘要

采用一种新方法制备中期染色体,通过原位免疫荧光检测抗5-甲基胞嘧啶抗体,与先前发表的方法相比,可显示新的富含5-甲基胞嘧啶的位点。在短期培养的淋巴细胞中,免疫荧光信号呈现出一种重复模式,可区分出四种结合位点。I型位点是次缢痕和一些近着丝粒区域,II型位点对应于T带。I型和II型位点均发出强烈荧光。III型位点形成R带模式并发出较弱荧光。IV型位点是近端着丝粒染色体的短臂,它们发出强烈但多态性的信号。对照实验结果表明,观察到的模式更像是富含5-甲基胞嘧啶位点分布不均的表现,而非所用各种处理的结果。在已知5-甲基胞嘧啶含量降低的淋巴母细胞系中,有可能证明染色体结构之间存在异质性低甲基化,主要涉及I型位点。该方法为在染色体上原位研究病理条件下甲基化的区域变化提供了可能性。

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