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利用互补DNA克隆证明牛角蛋白基因的细胞类型特异性表达。

Cell type-specific expression of bovine keratin genes as demonstrated by the use of complementary DNA clones.

作者信息

Jorcano J L, Magin T M, Franke W W

出版信息

J Mol Biol. 1984 Jun 15;176(1):21-37. doi: 10.1016/0022-2836(84)90380-2.

Abstract

Cytokeratins are a family of polypeptides that form the intermediate-sized filament characteristic of epithelial cells. The cytoskeletons of different types of epithelial cells have been reported to possess specific combinations of the members of this protein family. Therefore, we have sought to examine the correspondence between such differential protein expression and the expression of cytokeratin genes at the nucleic acid level. A library of recombinant plasmids carrying cDNA sequences synthesized from bovine epidermal mRNAs was constructed. Clones of about 10(3) base-pairs coding for all the major epidermal keratins of molecular weights of 50,000, 54,000, 59,000, 60,000 and 68,000 were identified by means of hybridization-selection, followed by one and two-dimensional gel electrophoresis of products of translation in vitro. Under stringent conditions, each of these clones hybridizes specifically with its corresponding mRNA and does not show significant cross-hybridization with mRNAs coding for the other keratins, including those belonging to the same subfamily. Using these clones in RNA blot hybridization analysis, we have studied the expression of keratin genes in diverse bovine epithelial tissues (muzzle epidermis, cornea, esophagus, bladder urothelium, liver) and cultured cell lines from kidney (MDBK) and mammary gland (BMGE + H, BMGE -H). In each case we have found a correlation between the respective keratin polypeptides and the corresponding mRNAs. Whereas mRNA coding for keratins Ia and VIb have been found only in epidermis, genes coding for other epidermal keratins are expressed also in certain non-epidermal epithelia and in cells of the BMGE + H line. In contrast, epidermal keratin mRNA sequences have not been detected in liver or bladder tissue, nor in cultured kidney cells (MDBK) or mammary gland cells of the BMGE - H line, which all express a set of cytokeratin polypeptides entirely different from those of epidermis. In all cases, only one mRNA size species has been found, suggesting that in different cell types the same mRNA species is synthesized from the same keratin gene. We conclude that the mechanisms controlling the cell type-specific synthesis of the diverse keratin genes act at a pre-translational level.

摘要

细胞角蛋白是一类多肽,它们构成上皮细胞特有的中等大小的丝状结构。据报道,不同类型上皮细胞的细胞骨架具有该蛋白家族成员的特定组合。因此,我们试图在核酸水平上研究这种差异蛋白表达与细胞角蛋白基因表达之间的对应关系。构建了一个携带从牛表皮mRNA合成的cDNA序列的重组质粒文库。通过杂交筛选,随后对体外翻译产物进行一维和二维凝胶电泳,鉴定出编码分子量为50,000、54,000、59,000、60,000和68,000的所有主要表皮角蛋白的约10³个碱基对的克隆。在严格条件下,这些克隆中的每一个都与其相应的mRNA特异性杂交,并且与编码其他角蛋白(包括属于同一亚家族的角蛋白)的mRNA没有明显的交叉杂交。使用这些克隆进行RNA印迹杂交分析,我们研究了角蛋白基因在不同牛上皮组织(口鼻表皮、角膜、食管、膀胱尿路上皮、肝脏)以及来自肾脏(MDBK)和乳腺(BMGE + H、BMGE -H)的培养细胞系中的表达。在每种情况下,我们都发现了各自的角蛋白多肽与相应mRNA之间的相关性。虽然编码角蛋白Ia和VIb的mRNA仅在表皮中发现,但编码其他表皮角蛋白的基因也在某些非表皮上皮以及BMGE + H系细胞中表达。相比之下,在肝脏或膀胱组织中,以及在BMGE - H系的培养肾细胞(MDBK)或乳腺细胞中均未检测到表皮角蛋白mRNA序列,这些细胞均表达一组与表皮完全不同的细胞角蛋白多肽。在所有情况下,仅发现一种mRNA大小的种类,这表明在不同细胞类型中,相同的mRNA种类是由相同的角蛋白基因合成的。我们得出结论,控制不同角蛋白基因细胞类型特异性合成的机制作用于翻译前水平。

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