Lin S Y, Chen Y J, Chang J G
Graduate Institute of Medical Science, Taipei Medical College and Department of Internal Medicine, Taipei Medical College Hospital, Taiwan.
J Gastroenterol Hepatol. 1998 Nov;13(11):1111-4. doi: 10.1111/j.1440-1746.1998.tb00585.x.
The candidate tumour suppressor gene TSG101, located on chromosome 11p15, has been associated with frequent intragenic deletion in uncultured primary human breast cancers. Using paired tumour and normal tissues from surgical specimens, we performed nested reverse transcriptase-polymerase chain reaction and direct sequencing to analyse TSG101 exons 1-6 from 32 gastric, 30 colorectal and 16 oesophageal cancers. Truncated transcripts, were found in both tumour and normal tissues from the stomach (15.6 and 12.5%), colon (13.3 and 3.3%) and oesophagus (25 and 25%). Multiple truncated transcripts in individual specimens were also observed. Two types of splicing patterns, one with three to six bases homology at the deletion junction (25.9%), the other with donor site 5' GT and acceptor site 3' AG (55.6%), were the most common patterns. We conclude that in gastrointestinal cancers, truncated transcripts of TSG101 gene occur not uncommonly and do so with a specific splicing pattern.
候选肿瘤抑制基因TSG101定位于11号染色体p15区域,与未经培养的原发性人类乳腺癌频繁的基因内缺失有关。我们利用手术标本中的配对肿瘤组织和正常组织,通过巢式逆转录聚合酶链反应和直接测序,分析了32例胃癌、30例结直肠癌和16例食管癌中TSG101基因的外显子1至6。在来自胃(分别为15.6%和12.5%)、结肠(分别为13.3%和3.3%)和食管(均为25%)的肿瘤组织和正常组织中均发现了截短的转录本。在单个标本中也观察到多个截短的转录本。两种剪接模式最为常见,一种在缺失连接处有三到六个碱基的同源性(25.9%),另一种在供体位点为5' GT,受体位点为3' AG(55.6%)。我们得出结论,在胃肠道癌中,TSG101基因的截短转录本并不罕见,且具有特定的剪接模式。