Gutman A, Kornblihtt A R
Instituto de Investigaciones en Ingeniería Genética y Biología Molecular (INGEBI-CONICET), Buenos Aires, Argentina.
Proc Natl Acad Sci U S A. 1987 Oct;84(20):7179-82. doi: 10.1073/pnas.84.20.7179.
We describe here a third region of variability in human fibronectin (FN) due to alternative RNA splicing. Two other positions of alternative splicing have been reported previously (ED and IIICS). The third region involves a 273-nucleotide exon encoding exactly one 91-amino acid repeat of type III homology, located between the DNA- and the cell-binding domains of FN, which is either included in or excluded from FN mRNA. The two mRNA variants arising by an exon-skipping mechanism are present in cells known to synthesize the cellular form of FN. However, liver cells, which are the source of plasma FN, produce only messengers without the extra type III sequence. Therefore, the region described here resembles, both structurally and functionally, the previously described ED (for extra domain) region, located toward the C terminus of the molecule, between the cell- and heparin- (hep 2) binding domains. We conclude that both the extra type III repeat (named EDII) and ED represent sequences restricted to cellular FN. Combination of all the possible patterns of splicing in the three regions described to date may generate up to 20 distinct FN polypeptides from a single gene.
我们在此描述了由于可变RNA剪接导致的人纤连蛋白(FN)的第三个可变区。先前已报道了另外两个可变剪接位置(ED和IIICS)。第三个区域涉及一个273个核苷酸的外显子,其精确编码一个91个氨基酸的III型同源重复序列,位于FN的DNA结合域和细胞结合域之间,该外显子在FN mRNA中要么被包含要么被排除。通过外显子跳跃机制产生的两种mRNA变体存在于已知合成细胞形式FN的细胞中。然而,作为血浆FN来源的肝细胞仅产生没有额外III型序列的信使RNA。因此,这里描述的区域在结构和功能上类似于先前描述的ED(额外结构域)区域,该区域位于分子的C末端,在细胞结合域和肝素(hep 2)结合域之间。我们得出结论,额外的III型重复序列(命名为EDII)和ED都代表仅限于细胞FN的序列。迄今为止描述的三个区域中所有可能的剪接模式组合可能从单个基因产生多达20种不同的FN多肽。