Khatri I A, Forstner G G, Forstner J F
Department of Biochemistry, Hospital for Sick Children, Toronto, Ontario, Canada.
Biochem J. 1993 Sep 1;294 ( Pt 2)(Pt 2):391-9. doi: 10.1042/bj2940391.
In the present report we describe the isolation and sequence of a partial cDNA (M2-798) for a rat intestinal mucin designated M2. A rat intestinal lambda ZAP II cDNA library was screened using a polyclonal antiserum which was prepared against deglycosylated high-molecular-mass glycopeptides of the purified mucin. Mucin cDNA clones were found to contain tandem repeats of 18 nt which encoded a threonine- and proline-rich peptide having a consensus sequence of TTTPDV. This is the same sequence reported recently by Gum, Hicks, Lagace, Byrd, Toribara, Siddiki, Fearney, Lamport and Kim [(1991) J. Biol. Chem. 266, 22733-22738] for a rat intestinal cDNA called RMUC 176. A novel feature present in the cDNA M2-798 is a 246 nt unique region at the 3' end which encodes a hydrophobic sequence of 82 amino acids. RNA blots probed with M2-798 cDNA produced a single hybridization band between 7.5 and 9.0 kb in rat small intestine and colon. An identical hybridization pattern was obtained with a PCR-generated cDNA probe corresponding solely to the unique hydrophobic region of M2-798, demonstrating that this region is encoded by the authentic M2 mRNA. Our data suggest that the unique region of M2 has the potential to be either a transmembrane region, or a domain which mediates hydrophobic interactions of the mucin with other molecules. Since we have previously reported another rat intestinal cDNA which encodes the C-terminus of a mucin-like peptide (MLP) [Xu, Wang, Huan, Cutz, Forstner and Forstner (1992) Biochem. J. 286, 335-338], we wished to discover whether M2 was encoded by the same gene. RNA blotting experiments with probes specific for M2 and MLP showed different mRNAs for each. The message for M2 (7.5-8.5 kb) was smaller than that for MLP (> 9.5 kb) and, unlike MLP, gave no signal in human colonic LS174T cells. The results of DNA blots probed with M2-798 and an MLP-probe suggest that M2 and MLP are likely to be single-copy genes. It would appear therefore that normal rat intestine, like human intestine, may express two different mucin genes.
在本报告中,我们描述了一种名为M2的大鼠肠道粘蛋白的部分cDNA(M2 - 798)的分离及测序情况。使用针对纯化粘蛋白的去糖基化高分子量糖肽制备的多克隆抗血清,对大鼠肠道λZAP II cDNA文库进行筛选。发现粘蛋白cDNA克隆含有18个核苷酸的串联重复序列,该序列编码一种富含苏氨酸和脯氨酸的肽段,其共有序列为TTTPDV。这与Gum、Hicks、Lagace、Byrd、Toribara、Siddiki、Fearney、Lamport和Kim近期报道的[(1991) J. Biol. Chem. 266, 22733 - 22738]一种名为RMUC 176的大鼠肠道cDNA的序列相同。cDNA M2 - 798中一个新的特征是3'端有一个246个核苷酸的独特区域,该区域编码一个由82个氨基酸组成的疏水序列。用M2 - 798 cDNA探针进行RNA印迹分析,在大鼠小肠和结肠中产生了一条7.5至9.0 kb之间的单一杂交带。用仅对应于M2 - 798独特疏水区域的PCR生成的cDNA探针获得了相同的杂交模式,表明该区域由真实的M2 mRNA编码。我们的数据表明,M2的独特区域有可能是一个跨膜区域,或者是一个介导粘蛋白与其他分子发生疏水相互作用的结构域。由于我们之前报道过另一种编码类粘蛋白肽(MLP)C末端的大鼠肠道cDNA [Xu, Wang, Huan, Cutz, Forstner和Forstner (1992) Biochem. J. 286, 335 - 338],我们希望了解M2是否由同一基因编码。用针对M2和MLP的特异性探针进行RNA印迹实验,结果显示它们各自具有不同的mRNA。M2的信使核糖核酸(7.5 - 8.5 kb)比MLP的(> 9.5 kb)小,并且与MLP不同,在人结肠LS174T细胞中没有信号。用M2 - 798和MLP探针进行DNA印迹分析的结果表明,M2和MLP可能是单拷贝基因。因此,正常大鼠肠道似乎与人肠道一样,可能表达两种不同的粘蛋白基因。