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小鼠FGF-1和FGF-1.A mRNA在胚胎发育期间及衰老心脏中的表达。

Expression of the mouse FGF-1 and FGF-1.A mRNAs during embryonic development and in the aging heart.

作者信息

Madiai F, Hackshaw K

机构信息

Department of Internal Medicine, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

Res Commun Mol Pathol Pharmacol. 2002;112(1-4):139-44.

Abstract

The mouse Fgf-1 gene contains at least four upstream promoters that are alternatively spliced to the first protein coding exon, giving rise to different Fgf-1 mRNA variants (1.A, 1.B, 1.C, and 1.G), each expressed in a tissue specific manner. Only the Fgf-1.A promoter contains TATA and CAAT consensus sequences, and its corresponding mRNA is mainly expressed in the mouse heart. In situ hybridization with an Fgf-1.A-specific cRNA probe showed the 1.A message to be very low in embryonic heart, tongue, spinal cord and smooth muscle of the small intestine. Moderate 1.A mRNA levels were revealed in head mesenchyme, paraxial mesoderm, in the embryonic inferior cunniculus, hyppocampus, and thymus. These results suggest a limited role of the Fgf-1.A mRNA variant during development.

摘要

小鼠Fgf-1基因包含至少四个上游启动子,这些启动子可选择性剪接至第一个蛋白质编码外显子,产生不同的Fgf-1 mRNA变体(1.A、1.B、1.C和1.G),每种变体均以组织特异性方式表达。只有Fgf-1.A启动子包含TATA和CAAT共有序列,其相应的mRNA主要在小鼠心脏中表达。用Fgf-1.A特异性cRNA探针进行原位杂交显示,1.A信息在胚胎心脏、舌头、脊髓和小肠平滑肌中非常低。在头部间充质、近轴中胚层、胚胎下鼻甲、海马体和胸腺中发现了中等水平的1.A mRNA。这些结果表明Fgf-1.A mRNA变体在发育过程中的作用有限。

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