Oyama F, Murata Y, Suganuma N, Kimura T, Titani K, Sekiguchi K
Laboratory of Biomedical Polymer Science, Fujita-Gakuen Health University School of Medicine, Aichi, Japan.
Biochemistry. 1989 Feb 7;28(3):1428-34. doi: 10.1021/bi00429a072.
Alternative splicing of fibronectin pre-mRNA at two distinct regions, termed ED-A and IIICS, was investigated with human adult and fetal tissues by the nuclease S1 protection assay. A clear tissue specificity was observed in the splicing pattern at the ED-A region. More ED-A+ than ED-A- mRNAs were identified in lung, whereas ED-A- mRNAs were predominantly expressed in liver. Endometrium contained nearly equal amounts of ED-A+ and ED-A- mRNAs. The splicing pattern at the ED-A region was also different between adult and fetal liver but not between adult and fetal lung. Tissue type specific splicing was also observed at the IIICS region. Although the mRNA species containing the complete IIICS sequence comprised 40-65% of the total fibronectin mRNAs irrespective of tissue types, expression of the mRNA species lacking a part or all of the IIICS sequence was more pronounced in adult liver than in other tissues including fetal liver. These results strongly suggest that the alternative splicing of fibronectin pre-mRNA in vivo is regulated in a tissue type specific manner at both the ED-A and IIICS regions and that it is developmentally regulated in liver but not in lung. On the basis of these and other observations reported previously, a possibility that a part of the fibronectins synthesized and secreted by hepatocytes is deposited in the tissue matrix is discussed.
通过核酸酶S1保护试验,利用成人和胎儿组织研究了纤连蛋白前体mRNA在两个不同区域(称为ED - A和IIICS)的可变剪接。在ED - A区域的剪接模式中观察到明显的组织特异性。在肺中鉴定出的ED - A + mRNA比ED - A - mRNA更多,而ED - A - mRNA主要在肝脏中表达。子宫内膜中ED - A +和ED - A - mRNA的含量几乎相等。ED - A区域的剪接模式在成人和胎儿肝脏之间也有所不同,但在成人和胎儿肺之间没有差异。在IIICS区域也观察到组织类型特异性剪接。尽管无论组织类型如何,包含完整IIICS序列的mRNA种类占纤连蛋白总mRNA的40 - 65%,但缺乏部分或全部IIICS序列的mRNA种类在成人肝脏中的表达比在包括胎儿肝脏在内的其他组织中更明显。这些结果强烈表明,纤连蛋白前体mRNA在体内的可变剪接在ED - A和IIICS区域均以组织类型特异性方式受到调控,并且在肝脏中受到发育调控,而在肺中则不然。基于这些以及先前报道的其他观察结果,讨论了肝细胞合成和分泌的一部分纤连蛋白沉积在组织基质中的可能性。