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小鼠p36(膜联蛋白II)基因的完整结构。鉴定小鼠和人类基因带有可变剪接5'非编码外显子的mRNA。

Complete structure of the murine p36 (annexin II) gene. Identification of mRNAs for both the murine and the human gene with alternatively spliced 5' noncoding exons.

作者信息

Fey M F, Moffat G J, Vik D P, Meisenhelder J, Saris C J, Hunter T, Tack B F

机构信息

The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Biochim Biophys Acta. 1996 May 2;1306(2-3):160-70. doi: 10.1016/0167-4781(95)00238-3.

Abstract

p36 (also termed annexin II) is a 39 kDa Ca2+/phospholipid-binding, membrane-associated protein that is a protein-tyrosine kinase substrate. We report here studies of the noncoding exons of p36, which combined with our earlier studies of the coding exons, allow us to conclude that the murine p36 gene is 34 kb in length with 14 exons. Comparison of the genes coding for mouse and human p36 (annexin II) and mouse, rat and human p35 (annexin I) and pigeon cp35 (an annexin I-related protein) shows strong genomic structural conservation supporting the hypothesis that these genes had a common ancestor. Both human and murine p36 mRNAs were found to be alternatively spliced in their 5' noncoding region. In both cases exon 2 is a cassette exon, which is present in a small fraction of p36 mRNAs. In type 1 mouse p36 mRNA the first noncoding 44 base exon 1 is joined to exon 3, the first of the 12 coding exons. In type 2 mRNA a 70 base noncoding exon (exon 2) is inserted between exon 1 and exon 3. Type 1 mRNA was present in all cell types studied as revealed by Northern analysis and primer extension, whereas type 2 mRNA could only be detected by RACE or PCR, indicating that it is of very low abundance. The major transcription start site of the mouse p36 gene was mapped by primer extension to be 61 bp upstream of the AUG initiation codon, which corresponds to type 1 mRNA, The murine p36 gene enhancer/promoter region contains a putative TATA box and several other potential regulatory sequences. The two alternatively-spliced human p36 mRNAs differ by the presence or absence of a noncoding 81 base exon (exon 2) inserted after exon 1, with exon 2-containing mRNAs representing approximately 10% of total p36 mRNA. The 300 bp spanning the promoter and exons 1-3 of the human and murine p36 genes show strong sequence homology immediately before and after the major transcription start site except in the region corresponding to exon 2, where homology is more limited.

摘要

p36(也称为膜联蛋白II)是一种39 kDa的钙/磷脂结合膜相关蛋白,是一种蛋白酪氨酸激酶底物。我们在此报告对p36非编码外显子的研究,结合我们早期对编码外显子的研究,使我们得出结论,小鼠p36基因长度为34 kb,有14个外显子。对编码小鼠和人类p36(膜联蛋白II)以及小鼠、大鼠和人类p35(膜联蛋白I)和鸽子cp35(一种膜联蛋白I相关蛋白)的基因进行比较,显示出强烈的基因组结构保守性,支持这些基因有共同祖先的假说。发现人类和小鼠的p36 mRNA在其5'非编码区均存在可变剪接。在这两种情况下,外显子2都是一个盒式外显子,仅存在于一小部分p36 mRNA中。在1型小鼠p36 mRNA中,第一个非编码的44个碱基的外显子1与12个编码外显子中的第一个外显子3相连。在2型mRNA中,一个70个碱基的非编码外显子(外显子2)插入在外显子1和外显子3之间。通过Northern分析和引物延伸显示,1型mRNA存在于所有研究的细胞类型中,而2型mRNA只能通过RACE或PCR检测到,表明其丰度非常低。通过引物延伸将小鼠p36基因的主要转录起始位点定位在AUG起始密码子上游61 bp处,这与1型mRNA相对应。小鼠p36基因增强子/启动子区域包含一个假定的TATA盒和其他几个潜在的调控序列。两种可变剪接的人类p36 mRNA的区别在于外显子1之后是否插入了一个81个碱基的非编码外显子(外显子2),含外显子2的mRNA约占p36 mRNA总量的10%。跨越人类和小鼠p36基因启动子和外显子1 - 3的300 bp在主要转录起始位点前后显示出很强的序列同源性,但在对应于外显子2的区域同源性更有限。

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