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人类视网膜母细胞瘤中13q14带缺失的分子检测与鉴别

Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.

作者信息

Lalande M, Donlon T, Petersen R A, Liberfarb R, Manter S, Latt S A

出版信息

Cancer Genet Cytogenet. 1986 Oct;23(2):151-7.

PMID:3756834
Abstract

Five cloned DNA segments within or adjacent to human chromosome band 13q14 were mapped by a combination of in situ hybridization and DNA dosage blotting. The DNA was isolated from human retinoblastoma patients with deletions varying in size and precise location. One of these deletions occurred in mosaic form, requiring T-cell cloning to obtain cells uniformly containing the deletion and useful for blotting. Regions of overlap between the intervals on chromosome #13 deduced for each probe from the two different mapping methods permitted a more precise location for each, from which a physical ordering of these five probes could be obtained. This ordered set of probes constitutes the start of a grid spanning band 13q14 of potential use in the diagnosis and understanding of human retinoblastoma.

摘要

通过原位杂交和DNA剂量印迹相结合的方法,对人类染色体带13q14内部或附近的五个克隆DNA片段进行了定位。从患有大小和精确位置各不相同的缺失的人类视网膜母细胞瘤患者中分离出DNA。其中一个缺失以嵌合形式出现,需要进行T细胞克隆以获得均匀包含该缺失且可用于印迹的细胞。从两种不同的定位方法推导出来的每个探针在13号染色体上的区间之间的重叠区域,使得每个探针的定位更加精确,由此可以获得这五个探针的物理排序。这组有序的探针构成了一个跨越13q14带的网格的起点,该网格在人类视网膜母细胞瘤的诊断和理解中具有潜在用途。

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