Mengle-Gaw L, Rabbitts T H
Medical Research Council, Laboratory of Molecular Biology, Cambridge, UK.
EMBO J. 1987 Jul;6(7):1959-65. doi: 10.1002/j.1460-2075.1987.tb02458.x.
We describe a region of human chromosome 8q24 involved in variant Burkitt's lymphoma translocations, and where an interstitial deletion occurs in an HTLV-I+ ATL and three c-myc amplicons terminate. The deletion in the ATL DNA begins within 1.3 kb of the cloned Burkitt's lymphoma translocation breakpoint and ends within 700 bases of the cloned human equivalent of the rat retroviral insertion site, mis-1. In addition, three c-myc amplicons terminate in this region and the end of one of these (the colon carcinoma COL0320) maps within 12 kb of the distal end of the ATL deletion. This region is probably approximately 300 kb downstream of c-myc and the consistent occurrence of abnormalities in this region implies involvement in tumour aetiology in several different cell types.
我们描述了人类8号染色体q24区域,该区域参与了变异型伯基特淋巴瘤的易位,在成人T细胞白血病病毒I型(HTLV-I)阳性的成人T细胞白血病(ATL)中发生了间质性缺失,并且三个c-myc扩增子在此终止。ATL DNA中的缺失始于克隆的伯基特淋巴瘤易位断点的1.3 kb范围内,止于克隆的与大鼠逆转录病毒插入位点mis-1的人类等效序列的700个碱基范围内。此外,三个c-myc扩增子在此区域终止,其中一个(结肠癌COL0320)的末端位于ATL缺失远端的12 kb范围内。该区域可能位于c-myc下游约300 kb处,并且该区域异常情况的持续出现表明其参与了几种不同细胞类型的肿瘤病因学。