Microscopy and image analysis of fibre-FISH

Hans Vrolijk, Ralph J Florijn, Frans M van de Rijke, Gert-Jan B van Ommen, Johan T den Dunnen, Anton K Raap, Hans J Tanke
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引用次数: 6

Abstract

In this paper the aspects of image acquisition, processing and analysis for DNA-fibre mapping are described. As the nature and the quality of the fibre-FISH signals (given its resolution range of 1–500 kb) may vary to a great extent, an interactive approach was chosen for the selection and analysis of the fibres. The accuracy of this fibre-FISH mapping approach was compared with restriction mapping on the basis of a map of seven cosmid contigs from the thyroglobulin gene, which spans about 300 kb. The results were in full agreement with restriction mapping. Standard errors for sizes of the cosmids, gaps, and overlaps were obtained between 2.0 and 6.2 kb. By alternately labelling the clones of the DNA map a colour barcode can be composed which eases the identification of gene rearrangements, as is illustrated on two patients with a deletion in the Duchenne muscular dystrophy (DMD) gene. The time needed for straightening a fibre and defining the distances between the different cosmids is dominated by the amount of human interaction and typically takes 1–2 min. From this study it is clear that fibre-FISH analysis is well suited for mapping cosmid contigs and defining breakpoints in patient material with the same or better accuracy as restriction mapping and PCR analysis.

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纤维FISH的显微镜和图像分析
本文介绍了DNA纤维图谱的图像采集、处理和分析。由于纤维FISH信号的性质和质量(给定其1–500 kb的分辨率范围)可能会有很大的变化,因此选择了一种交互式方法来选择和分析纤维。将这种纤维FISH作图方法的准确性与基于来自甲状腺球蛋白基因的七个粘粒重叠群的图谱的限制性作图进行比较,该图谱跨度约300kb。结果与限制映射完全一致。获得的粘粒大小、间隙和重叠的标准误差在2.0和6.2kb之间。通过交替标记DNA图谱的克隆,可以组成彩色条形码,这有助于识别基因重排,如两名Duchenne肌营养不良(DMD)基因缺失的患者所示。拉直纤维和确定不同粘粒之间距离所需的时间主要由人类相互作用的量决定,通常需要1-2分钟。从这项研究中可以清楚地看出,纤维FISH分析非常适合绘制粘粒重叠群和在患者材料中定义断点,其准确度与限制性作图和PCR分析相同或更好。
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