Bicknell D C, Rowan A, Bodmer W F
Cancer Immunology Laboratory, John Radcliffe Hospital, Headington, Oxford, United Kingdom.
Proc Natl Acad Sci U S A. 1994 May 24;91(11):4751-5. doi: 10.1073/pnas.91.11.4751.
The technique of single-strand conformation polymorphism (SSCP) was used to screen a series of 37 established colorectal cell lines, 22 fresh tumor samples, and 22 normal DNA samples for mutations in the beta 2-microglobulin gene. Exon 1 (including the leader peptide sequence) and exon 2 were screened separately. Six of 37 colorectal cell lines and 1 of 22 fresh tumors were shown to contain mutations, whereas no mutations were detected in the normal DNA samples. Sequencing of these mutations showed that an 8-bp CT repeat in the leader peptide sequence was particularly variable, since 3 of the cell lines and one fresh tumor sample have deletions in this region. In the related cell lines, DLD-1 and HCT-15, two similar mutations were identified, a C-->A substitution in codon 10 and a G-->T mutation in the splice sequence of intron 1. Expression of beta 2-microglobulin was examined using a series of monoclonal antibodies in an ELISA system. Reduced expression correlated with a mutation in one allele of beta 2-microglobulin, whereas loss of expression was seen in instances where a line was homozygous for a mutation or heterozygous for two mutations.
采用单链构象多态性(SSCP)技术,对37株已建立的结肠直肠癌细胞系、22份新鲜肿瘤样本和22份正常DNA样本进行筛查,以检测β2-微球蛋白基因的突变情况。分别对第1外显子(包括前导肽序列)和第2外显子进行筛查。结果显示,37株结肠直肠癌细胞系中有6株、22份新鲜肿瘤样本中有1株含有突变,而在正常DNA样本中未检测到突变。对这些突变进行测序发现,前导肽序列中的一个8碱基对CT重复序列特别多变,因为有3株细胞系和1份新鲜肿瘤样本在该区域存在缺失。在相关细胞系DLD-1和HCT-15中,鉴定出两个相似的突变,即密码子10处的C→A替换和第1内含子剪接序列中的G→T突变。在ELISA系统中,使用一系列单克隆抗体检测β2-微球蛋白的表达。β2-微球蛋白表达降低与β2-微球蛋白一个等位基因的突变相关,而在细胞系对一个突变纯合或对两个突变杂合的情况下,可观察到表达缺失。