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人类染色体8p22带纯合缺失区域内一个基因的结构与甲基化相关沉默

Structure and methylation-associated silencing of a gene within a homozygously deleted region of human chromosome band 8p22.

作者信息

MacGrogan D, Levy A, Bova G S, Isaacs W B, Bookstein R

机构信息

Canji, Inc., 3030 Science Park Road, San Diego, California, 92121, USA.

出版信息

Genomics. 1996 Jul 1;35(1):55-65. doi: 10.1006/geno.1996.0322.

DOI:10.1006/geno.1996.0322
PMID:8661104
Abstract

The structure and expression pattern of a human gene located within a homozygously deleted region of a metastatic prostate cancer have been characterized. Multiple cDNA fragments of this gene were isolated by hybrid capture with yeast artificial chromosome clones covering the deletion region. Eleven coding exons spanned 205-220 kb of the 730- to 970-kb deletion. The predicted amino acid sequence was 43% identical to that of an anonymous Caenorhabditis elegans gene and 20% identical to an accessory or regulatory subunit of the oligosaccharyltransferase enzyme complex in Saccharomyces cerevisiae. Hydrophobicity profiles of all three gene products were similar and showed four putative membrane-spanning domains in the molecules' C-terminal halves, suggesting a general conservation of function. The gene was expressed as an approximately 1.5-kb mRNA in most nonlymphoid human cells/tissues including prostate, lung, liver, and colon. Expression was detected in many epithelial tumor cell lines, but was undetectable by Northern blot or RT-PCR in 14 of 15 colorectal, 1 of 8 lung, and 1 of 4 liver cancer cell lines. Lack of expression in tumor cell lines was highly correlated with hypermethylation of a CpG island located at the gene's 5' end. These findings form a basis for further work on this candidate tumor suppressor gene.

摘要

对位于转移性前列腺癌纯合缺失区域内的一个人类基因的结构和表达模式进行了表征。通过与覆盖缺失区域的酵母人工染色体克隆进行杂交捕获,分离出了该基因的多个cDNA片段。11个编码外显子跨越了730至970kb缺失区域中的205至220kb。预测的氨基酸序列与一个未知的秀丽隐杆线虫基因的序列有43%的同一性,与酿酒酵母中寡糖基转移酶复合物的一个辅助或调节亚基有20%的同一性。所有这三种基因产物的疏水性图谱相似,并且在分子的C端一半显示出四个推定的跨膜结构域,这表明功能存在普遍保守性。该基因在包括前列腺、肺、肝和结肠在内的大多数非淋巴细胞人类细胞/组织中表达为约1.5kb的mRNA。在许多上皮肿瘤细胞系中检测到了表达,但在15个结肠直肠癌细胞系中的14个、8个肺癌细胞系中的1个以及4个肝癌细胞系中的1个中,通过Northern印迹或RT-PCR未检测到表达。肿瘤细胞系中表达的缺失与位于该基因5'端的一个CpG岛的高甲基化高度相关。这些发现为进一步研究这个候选肿瘤抑制基因奠定了基础。

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