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重金属反应转录因子MTF-1的小鼠基因特征分析

Characterization of the mouse gene for the heavy metal-responsive transcription factor MTF-1.

作者信息

Auf der Maur A, Belser T, Wang Y, Günes C, Lichtlen P, Georgiev O, Schaffner W

机构信息

Institute of Molecular Biology, University of Zürich, Switzerland.

出版信息

Cell Stress Chaperones. 2000 Jul;5(3):196-206. doi: 10.1379/1466-1268(2000)005<0196:cotmgf>2.0.co;2.

Abstract

MTF-1 is a zinc finger transcription factor that mediates the cellular response to heavy metal stress; its targeted disruption in the mouse leads to liver decay and embryonic lethality at day E14. Recently, we have sequenced the entire MTF-1 gene in the compact genome of the pufferfish Fugu rubripes. Here we have defined the promoter sequences of human and mouse MTF-1 and the genomic structure of the mouse MTF-1 locus. The transcription unit of MTF-1 spans 42 kb (compared to 8.5 kb in Fugu) and is located downstream of the gene for a phosphatase (INPP5P) in mouse, human, and fish. In all of these species, the MTF promoter region has the features of a CpG island. In both mouse and human, the 5' untranslated region harbors conserved short reading frames of unknown function. RNA mapping experiments revealed that in these two species, MTF-1 mRNA is transcribed from a cluster of multiple initiation sites from a TATA-less promoter without metal-responsive elements. Transcription from endogenous and transfected MTF-1 promoters was not affected by heavy metal load or other stressors, in support of the notion that MTF-1 activity is regulated at the posttranscriptional level. Tissue Northern blots normalized for poly A+ RNA indicate that MTF-1 is expressed at similar levels in all tissues, except in the testes, that contain more than 10-fold higher mRNA levels.

摘要

金属反应转录因子1(MTF-1)是一种锌指转录因子,可介导细胞对重金属应激的反应;在小鼠中对其进行靶向破坏会导致肝脏衰退以及在胚胎发育第14天出现胚胎致死性。最近,我们已对河豚红鳍东方鲀紧凑基因组中的整个MTF-1基因进行了测序。在此,我们确定了人类和小鼠MTF-1的启动子序列以及小鼠MTF-1基因座的基因组结构。MTF-1的转录单元跨度为42 kb(相比之下,河豚中为8.5 kb),在小鼠、人类和鱼类中位于一种磷酸酶(INPP5P)基因的下游。在所有这些物种中,MTF启动子区域都具有CpG岛的特征。在小鼠和人类中,5'非翻译区都含有功能未知的保守短读框。RNA定位实验表明,在这两个物种中,MTF-1 mRNA是从一个无TATA且无金属反应元件的启动子的多个起始位点簇转录而来。来自内源性和转染的MTF-1启动子的转录不受重金属负荷或其他应激源的影响,这支持了MTF-1活性在转录后水平受到调控的观点。针对聚腺苷酸加尾RNA进行标准化的组织Northern印迹表明,MTF-1在所有组织中的表达水平相似,但在睾丸中除外,睾丸中的mRNA水平要高出10倍以上。

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