Velcich A, Palumbo L, Selleri L, Evans G, Augenlicht L
Department of Oncology, Montefiore Medical Center/Albert Einstein Cancer Center, Bronx, New York 10467, USA.
J Biol Chem. 1997 Mar 21;272(12):7968-76. doi: 10.1074/jbc.272.12.7968.
The human MUC2 gene maps to chromosome 11p15, where three additional mucin genes have been located, and encodes the most abundant gastrointestinal mucin normally expressed in the intestinal goblet cell lineage. However, in pathological conditions, including colorectal cancer, MUC2 can be abnormally expressed. Therefore, it is of considerable interest to understand the regulation of the MUC2 gene and how the mechanism is altered in colon cancer. Toward this goal, we have isolated a group of overlapping clones (contig) spanning 85 kilobases harboring the entire MUC2 locus, including sequences located upstream of the gene. Detection of two DNase I-hypersensitive sites in the 5' region of the MUC2 gene suggests the presence of DNA regulatory elements. To better characterize this region, we have sequenced 12 kilobases of the upstream region and analyzed it for functional activity by cloning portions of it into a luciferase reporter vector and assaying for promoter/enhancer activity using a transient transfection assay. A fragment from the AUG translational initiation codon +1 to -848 confers maximal transcriptional activity in several intestinal cell lines. Elements located further upstream exert a negative effect on the expression of the reporter gene when tested in conjunction with homologous or heterologous promoters. The same pattern of expression is observed when the MUC2/luciferase constructs are transfected into HeLa cells, which do not express the endogenous MUC2 gene. However, the level of activity in HeLa cells is at least an order of magnitude higher, suggesting that additional sequences singularly or in combination are responsible for the tissue- and cell lineage-specific expression of MUC2. Finally, we have identified an additional mucin-like gene (MUCX), located upstream of MUC2. We show that this MUCX gene, that is transcribed in opposite orientation to that of MUC2, is expressed with a pattern distinct from that of MUC2, yet similar to that of MUC5B and MUC6, two additional mucin genes located at chromosome 11p15. Recent information on the order of the mucin genes at chromosome 11p15 suggests that MUCX may be MUC6, one of the already identified mucin genes, or a novel one, yet to be fully characterized.
人类MUC2基因定位于11号染色体p15区域,该区域还定位有另外三个黏蛋白基因,MUC2基因编码通常在肠道杯状细胞谱系中表达的最丰富的胃肠道黏蛋白。然而,在包括结直肠癌在内的病理情况下,MUC2可能会异常表达。因此,了解MUC2基因的调控以及结肠癌中该机制如何改变具有相当大的研究意义。为实现这一目标,我们分离出了一组重叠克隆(重叠群),其跨度为85千碱基,包含整个MUC2基因座,包括该基因上游的序列。在MUC2基因5'区域检测到两个对DNase I敏感的位点,这表明存在DNA调控元件。为了更好地表征该区域,我们对上游区域的12千碱基进行了测序,并通过将其部分片段克隆到荧光素酶报告载体中并使用瞬时转染试验检测启动子/增强子活性来分析其功能活性。从AUG翻译起始密码子+1到-848的一个片段在几种肠道细胞系中赋予最大转录活性。当与同源或异源启动子一起测试时,位于更上游的元件对报告基因的表达产生负面影响。当将MUC2/荧光素酶构建体转染到不表达内源性MUC2基因的HeLa细胞中时,观察到相同的表达模式。然而,HeLa细胞中的活性水平至少高一个数量级,这表明额外的序列单独或组合起来负责MUC2的组织和细胞谱系特异性表达。最后,我们在MUC2上游鉴定出了另一个类黏蛋白基因(MUCX)。我们发现这个MUCX基因与MUC2的转录方向相反,其表达模式与MUC2不同,但与位于11号染色体p15的另外两个黏蛋白基因MUC5B和MUC6相似。关于11号染色体p15上黏蛋白基因排列的最新信息表明,MUCX可能是已鉴定的黏蛋白基因之一MUC6,或者是一个尚未完全表征的新基因。