Menkes病基因的转录前和转录后调控

Edward D. Harris, Sudeep Majumdar
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引用次数: 1

摘要

Menkes病证明了铜(Cu)-ATP酶(ATP7A)在Cu的吸收和稳态中发挥主导作用。值得注意的是,Menkes病基因(MNK)的近端启动子区具有顺式活性元件,这些元件与转录因子的结合位点有关,已知酵母中的转录因子会被低Cu状态激活。对低铜的反应尚未被合理化为对Menkes基因表达的控制,但鉴于最近对人类铜吸收的研究,这似乎很重要。ATP7A基因产生了替代转录物,其中一种在5′端有一个插入物,其中包含一种结构域类似于高尔基体系留蛋白的蛋白质的序列信息。这引发了人们的猜测,即一种替代转录产物可能在调节ATP7A修饰的囊泡进入分泌途径方面具有重要的生物学功能。本文提供的证据支持启动子激活和选择性剪接,分别在转录前和转录后事件,在控制门氏病基因表达。J.Trace Elem。《实验医学》,16:181–1892003。©2003 Wiley-Liss,股份有限公司。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pre- and post-transcriptional regulation of the Menkes disease gene
Menkes disease is testament to a copper (Cu)-ATPase (ATP7A) playing a dominant role in the absorption and homeostasis of Cu. Significantly, the proximal promoter region of the Menkes disease gene (MNK) has cis-active elements that relate to binding sites for transcription factors which in yeast are known to be activated by a low Cu status. A response to low Cu has not been rationalized into the control of Menkes gene expression, but seems important in light of recent Cu absorption studies in humans. The ATP7A gene gives rises to alternative transcripts, one of which has an insert at the 5′ end with sequence information for a protein with a structural domain similar to a Golgi tethering protein. This has opened speculation that one alternative transcript product may have an important biological function in regulating the entrance of ATP7A laded vesicles into the secretory pathway. This paper presents evidence supporting promoter activation and alternative splicing, pre- and post-transcription events respectively, in the control of Menkes disease gene expression. J. Trace Elem. Exp. Med. 16:181–189, 2003. © 2003 Wiley-Liss, Inc.
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