Fairman J, Claxton D, Williman C L, Deisseroth A B, Nagarajan L
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
PCR Methods Appl. 1994 Aug;4(1):6-12. doi: 10.1101/gr.4.1.6.
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.
整条染色体的缺失或增加以及间质性缺失或扩增是几种造血系统肿瘤的特征。这些染色体异常可通过对骨髓穿刺液进行常规细胞遗传学分析来识别。我们利用位于5q31的白细胞介素-9(IL9)基因内的一个高度多态性二核苷酸重复序列,开发了一种基于聚合酶链反应(PCR)的检测方法,用于在伴有5q-染色体(5q间质性缺失)的髓系疾病模型系统中检测5q31位点的缺失。在给定样本中,利用磷光成像仪对各个等位基因的扩增进行定量,可将等位基因的表现表示为较大等位基因与较小等位基因的比率。对来自Ficoll漂浮层和沉淀层的配对DNA样本中这些比率进行比较,可为等位基因缺失提供证据。此处呈现的结果表明,这种同位素掺入比率比较技术可扩展用于研究造血肿瘤中的任何缺失或数目异常。