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转化生长因子-β调节纤连蛋白信使核糖核酸前体的剪接模式。

Transforming growth factor-beta regulates the splicing pattern of fibronectin messenger RNA precursor.

作者信息

Borsi L, Castellani P, Risso A M, Leprini A, Zardi L

机构信息

Cell Biology Laboratory, Instituto Nazionale per la Ricerca sul Cancro, Genova, Italy.

出版信息

FEBS Lett. 1990 Feb 12;261(1):175-8. doi: 10.1016/0014-5793(90)80664-5.

Abstract

Fibronectin (FN) polymorphism is caused by alternative splicing patterns in at least three regions (ED-A, ED-B and IIICS) of the primary transcript of a single gene. Using monoclonal antibodies, we previously demonstrated that transforming growth factor-beta (TGF-beta) preferentially increases the accumulation of the FN isoforms containing the ED-A sequence in cultured normal human fibroblasts [Balza et al., (1988) FEBS Lett. 228, 42-44]. To determine the basis of this effect, we have examined through S1 nuclease analysis, the levels of ED-A- and ED-B-containing mRNAs in cultured normal human skin fibroblasts before and after TGF-beta treatment. These experiments have shown that TGF-beta increases the relative amount of m-RNA for ED-A- and ED-B-containing FN isoforms. These data demonstrate that a growth factor may regulate the splicing pattern of a pre-mRNA.

摘要

纤连蛋白(FN)多态性是由单个基因初级转录本至少三个区域(ED - A、ED - B和IIICS)的可变剪接模式引起的。我们先前使用单克隆抗体证明,转化生长因子-β(TGF-β)优先增加培养的正常人成纤维细胞中含有ED - A序列的FN同工型的积累[Balza等人,(1988年)《欧洲生物化学学会联合会快报》228,42 - 44]。为了确定这种效应的基础,我们通过S1核酸酶分析检测了TGF-β处理前后培养的正常人皮肤成纤维细胞中含ED - A和含ED - B的mRNA水平。这些实验表明,TGF-β增加了含ED - A和含ED - B的FN同工型的mRNA相对量。这些数据证明生长因子可能调节前体mRNA的剪接模式。

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