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在经5-氮杂胞苷或5-氮杂脱氧胞苷处理的人原B细胞系中优先诱导1号染色体多分支图形和整条臂缺失。

Preferential induction of chromosome 1 multibranched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidine.

作者信息

Hernandez R, Frady A, Zhang X Y, Varela M, Ehrlich M

机构信息

Hayward Genetics Center, Tulane Medical School, New Orleans, LA 70112, USA.

出版信息

Cytogenet Cell Genet. 1997;76(3-4):196-201. doi: 10.1159/000134548.

Abstract

5-Azacytidine (azaCR) causes genomic demethylation and decondensation of juxtacentromeric heterochromatin in chromosomes 1, 9, and 16. We determined the karyotypes of a pro-B cell line (FLEB14) treated with azaCR or its deoxynucleoside analog (azaCdR). About 80% of the induced rearrangements were in chromosome 1, and almost 90% of these involved its pericentromeric region. Multibranched figures with up to seven chromosome 1 arms, as well as whole-arm deletions of this chromosome, were the predominant anomalies, often with one normal homolog of chromosome 1 present. Isochromosomes 1 and fusions in the pericentromeric regions of chromosomes 1 and 16 or chromosomes 1 and 9 were also seen. The overlap of the spectrum of chromosomal rearrangements in azaCR- or azaCdR-treated FLEB14 cells and in mitogen-stimulated lymphocytes from patients with a rare genetic disease (ICF) associated with localized DNA hypomethylation supports the hypothesis that the DNA demethylating activity of azaCR is essential for the induction of these pericentromeric rearrangements. These studies may help elucidate the overrepresentation of chromosome 1 pericentromeric rearrangements in many types of cancer cells.

摘要

5-氮杂胞苷(azaCR)可导致1号、9号和16号染色体上近着丝粒异染色质的基因组去甲基化和解聚。我们确定了用azaCR或其脱氧核苷类似物(azaCdR)处理的前B细胞系(FLEB14)的核型。约80%的诱导重排发生在1号染色体上,其中近90%涉及其着丝粒周围区域。具有多达七条1号染色体臂的多分支图形以及该染色体的整条臂缺失是主要异常情况,通常会有一条1号染色体的正常同源染色体存在。还观察到1号等臂染色体以及1号与16号或1号与9号染色体着丝粒周围区域的融合。在经azaCR或azaCdR处理的FLEB14细胞以及来自患有与局部DNA低甲基化相关的罕见遗传病(ICF)患者的有丝分裂原刺激淋巴细胞中,染色体重排谱的重叠支持了以下假设:azaCR的DNA去甲基化活性对于诱导这些着丝粒周围重排至关重要。这些研究可能有助于阐明1号染色体着丝粒周围重排在多种癌细胞中过度出现的原因。

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