一种检测模型造血肿瘤中等位基因丢失的灵敏PCR方法的建立。

J Fairman, D Claxton, C L Williman, A B Deisseroth, L Nagarajan
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引用次数: 10

摘要

整个染色体的缺失或增加以及间质缺失或扩增是几种造血肿瘤的特征。这些染色体异常可以通过骨髓抽吸的常规细胞遗传学分析来确定。我们开发了一种基于pcr的检测方法,通过利用5q31上白细胞介素-9 (IL9)基因内高度多态性的二核苷酸重复,在5q-染色体(5q间质缺失)的髓系疾病模型系统中检测染色体5q31位点的缺失。在给定的样品中,磷酸化成像仪中单个等位基因的扩增量允许等位基因的表示以较大等位基因与较小等位基因的比例表示。从菲科尔浮力和颗粒状的成对DNA样本中比较这些比率提供了等位基因丢失的证据。本文的结果表明,这种比较同位素掺入比率的技术可以扩展到研究造血肿瘤中的任何缺失或数值异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a sensitive PCR to detect allele loss in a model hematopoietic neoplasm.

Loss or gain of an entire chromosome and interstitial deletions or amplifications are hallmarks of several hematopoietic neoplasms. These chromosomal anomalies can be identified by conventional cytogenetic analysis of bone marrow aspirates. We have developed a PCR-based assay to detect loss of chromosome 5q31 loci, in the model system of myeloid disorders with the 5q- chromosome (interstitial deletion of 5q), by taking advantage of a highly polymorphic dinucleotide repeat within the interleukin-9 (IL9) gene on 5q31. In a given sample, quantitation of amplification of individual alleles in a Phosphorimager allowed the representation of alleles to be expressed as a ratio of the larger to the smaller allele. Comparison of these ratios in paired DNA samples from Ficoll buoyant and pelletted fractions provides evidence for allele loss. Results presented here demonstrate that this technique of comparison of ratios of isotope incorporation could be expanded to Investigate any deletion or numerical abnormality in hematopoietic tumors.

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