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脆性位点、癌症染色体断点和癌基因都聚集在浅G带中。

Fragile sites, cancer chromosome breakpoints, and oncogenes all cluster in light G bands.

作者信息

Hecht F

机构信息

Genetics Center, Southwest Biomedical Research Institute, Scottsdale, Arizona 85251.

出版信息

Cancer Genet Cytogenet. 1988 Mar;31(1):17-24. doi: 10.1016/0165-4608(88)90005-2.

Abstract

Fragile sites tend to be bands where breaks occur in cancer chromosome rearrangements that can involve oncogenes. The locations of fragile sites, cancer breakpoints, and oncogenes were therefore charted. All were predominantly in light G bands. Specifically, 78 of 89 (88%) fragile sites were in light G bands including the large group of common fragile sites inducible with aphidicolin (p less than 0.001). Of 61 cancer breakpoints, 50 (82%) were in light bands including translocation breakpoints (p less than 0.001). Thirteen of 14 (93%) oncogenes localized to light bands. The sharing of chromosome bands can stem from a biologically meaningful relationship, as between cancer breakpoints and oncogenes. Joint occupancy of chromosome bands can also reflect independent reasons to be in the same sector of the genome. Thus, fragile sites may well be in light bands because they are associated with active genes. This clearly does not rule out a biologic relationship between specific fragile sites and specific cancer breakpoints.

摘要

脆性位点往往是癌症染色体重排过程中发生断裂的条带,这些重排可能涉及癌基因。因此,绘制了脆性位点、癌症断点和癌基因的位置图。所有这些主要都位于浅G带。具体而言,89个脆性位点中的78个(88%)位于浅G带,包括用阿非科林可诱导的一大组常见脆性位点(p<0.001)。在61个癌症断点中,50个(82%)位于浅带,包括易位断点(p<0.001)。14个癌基因中的13个(93%)定位于浅带。染色体条带的共享可能源于生物学上有意义的关系,如癌症断点和癌基因之间的关系。染色体条带的共同占据也可能反映了位于基因组同一区域的独立原因。因此,脆性位点很可能位于浅带,因为它们与活跃基因相关。这显然并不排除特定脆性位点与特定癌症断点之间的生物学关系。

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