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ptc1的过表达会抑制Shh靶基因的诱导,并阻止神经管的正常模式形成。

Overexpression of ptc1 inhibits induction of Shh target genes and prevents normal patterning in the neural tube.

作者信息

Goodrich L V, Jung D, Higgins K M, Scott M P

机构信息

Department of Developmental Biology, Stanford University School of Medicine, Stanford, California, 94305-5427, USA.

出版信息

Dev Biol. 1999 Jul 15;211(2):323-34. doi: 10.1006/dbio.1999.9311.

Abstract

Patched (Ptc) is a human tumor suppressor protein and a candidate receptor for Hedgehog (Hh) proteins, which regulate growth and patterning in embryos. Ptc represses expression of Hh target genes such as Gli1 and ptc1 itself. Localized secretion of Hh appears to induce transcription of target genes in specific patterns by binding to Ptc and preventing it from functioning in recipient cells. People who are heterozygous for PTC1 exhibit a range of developmental defects, suggesting that some genes are inappropriately expressed when there is not enough Ptc protein. To test the idea that a balance between Hh and Ptc activities is essential for normal development, we overexpressed Ptc in the neural tube. We find that excess Ptc is sufficient to inhibit expression of Gli1 and ptc1, suggesting that Sonic hedgehog (Shh) cannot signal effectively. This leads to partial dorsalization of the neural tube and a wide spectrum of neural defects, ranging from embryonic lethality to hydrocephaly.

摘要

patched(Ptc)是一种人类肿瘤抑制蛋白,也是刺猬蛋白(Hh)的候选受体,Hh蛋白在胚胎发育过程中调控生长和模式形成。Ptc抑制Hh靶基因如Gli1和ptc1自身的表达。Hh的局部分泌似乎通过与Ptc结合并阻止其在受体细胞中发挥作用,从而以特定模式诱导靶基因的转录。PTC1基因杂合的人表现出一系列发育缺陷,这表明当没有足够的Ptc蛋白时,一些基因会异常表达。为了验证Hh和Ptc活性之间的平衡对正常发育至关重要这一观点,我们在神经管中过表达了Ptc。我们发现过量的Ptc足以抑制Gli1和ptc1的表达,这表明音猬因子(Shh)无法有效发出信号。这导致神经管部分背化以及一系列神经缺陷,从胚胎致死到脑积水不等。

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