首页> 美国卫生研究院文献>Endocrinology >Direct Activation of Amidohydrolase Domain-Containing 1 Gene by Thyroid Hormone Implicates a Role in the Formation of Adult Intestinal Stem Cells During Xenopus Metamorphosis
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Direct Activation of Amidohydrolase Domain-Containing 1 Gene by Thyroid Hormone Implicates a Role in the Formation of Adult Intestinal Stem Cells During Xenopus Metamorphosis

机译:甲状腺激素直接激活含酰胺水解酶结构域的1基因暗示非洲爪蟾变态期间成人肠道干细胞形成中的作用。

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摘要

The T3-dependent anuran metamorphosis resembles postembryonic development in mammals, the period around birth when plasma T3 levels peak. In particular, the remodeling of the intestine during metamorphosis mimics neonatal intestinal maturation in mammals when the adult intestinal epithelial self-renewing system is established. We have been using intestinal metamorphosis to investigate how the organ-specific adult stem cells are formed during vertebrate development. Early studies in Xenopus laevis have shown that this process involves complete degeneration of the larval epithelium and de novo formation of adult stem cells. A tissue-specific microarray analysis of intestinal gene expression during Xenopus laevis metamorphosis has identified a number of candidate stem cell genes. Here we have carried out detailed analyses of one such gene, amidohydrolase domain containing 1 (AMDHD1) gene, which encodes an enzyme in the histidine catabolic pathway. We show that AMDHD1 is exclusively expressed in the proliferating adult epithelial stem cells during metamorphosis with little expression in other intestinal tissues. We further provide evidence that T3 activates AMDHD1 gene expression directly at the transcription level through T3 receptor binding to the AMDHD1 gene in the intestine. In addition, we have reported earlier that histidine ammonia-lyase gene, another gene in histidine catabolic pathway, is similarly regulated by T3 in the intestine. These results together suggest that histidine catabolism plays a critical role in the formation and/or proliferation of adult intestinal stem cells during metamorphosis.
机译:T3依赖的无色变态类似于哺乳动物的胚胎后发育,这是出生后血浆T3水平达到峰值的时期。特别地,当建立成年肠道上皮自我更新系统时,在变形过程中肠道的重塑可以模仿哺乳动物的新生肠道成熟。我们一直在使用肠道变态来研究脊椎动物发育过程中器官特异性成年干细胞的形成方式。爪蟾的早期研究表明,该过程涉及幼虫上皮的完全变性和成年干细胞的从头形成。爪蟾变态过程中肠道基因表达的组织特异性微阵列分析已鉴定出许多候选干细胞基因。在这里,我们对一种这样的基因进行了详细的分析,即含有1(AMDHD1)基因的酰胺水解酶结构域,该基因在组氨酸分解代谢途径中编码一种酶。我们显示,AMDHD1在变态过程中仅在增殖的成年上皮干细胞中表达,而在其他肠组织中几乎没有表达。我们进一步提供证据表明,T3通过与肠道中的AMDHD1基因结合的T3受体直接在转录水平上激活AMDHD1基因表达。另外,我们先前已经报道了组氨酸分解代谢途径中的另一个基因组氨酸氨裂合酶基因也受到肠中T3的类似调节。这些结果共同表明,组氨酸分解代谢在变态过程中在成年肠道干细胞的形成和/或增殖中起关键作用。

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