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Keap1基因缺失突变由于Nrf2的组成型激活导致出生后致死。

Keap1-null mutation leads to postnatal lethality due to constitutive Nrf2 activation.

作者信息

Wakabayashi Nobunao, Itoh Ken, Wakabayashi Junko, Motohashi Hozumi, Noda Shuhei, Takahashi Satoru, Imakado Sumihisa, Kotsuji Tomoe, Otsuka Fujio, Roop Dennis R, Harada Takanori, Engel James Douglas, Yamamoto Masayuki

机构信息

Center for Tsukuba Advanced Research Alliance, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba 305-8577, Japan.

出版信息

Nat Genet. 2003 Nov;35(3):238-45. doi: 10.1038/ng1248. Epub 2003 Sep 28.

Abstract

Transcription factor Nrf2 (encoded by Nfe2l2) regulates a battery of detoxifying and antioxidant genes, and Keap1 represses Nrf2 function. When we ablated Keap1, Keap1-deficient mice died postnatally, probably from malnutrition resulting from hyperkeratosis in the esophagus and forestomach. Nrf2 activity affects the expression levels of several squamous epithelial genes. Biochemical data show that, without Keap1, Nrf2 constitutively accumulates in the nucleus to stimulate transcription of cytoprotective genes. Breeding to Nrf2-deficient mice reversed the phenotypic Keap1 deficiencies. These experiments show that Keap1 acts upstream of Nrf2 in the cellular response to oxidative and xenobiotic stress.

摘要

转录因子Nrf2(由Nfe2l2编码)调控一系列解毒和抗氧化基因,而Keap1抑制Nrf2的功能。当我们敲除Keap1时,Keap1基因缺失的小鼠出生后死亡,可能是由于食管和前胃的角化过度导致营养不良。Nrf2活性影响几种鳞状上皮基因的表达水平。生化数据表明,没有Keap1时,Nrf2在细胞核中持续积累,以刺激细胞保护基因的转录。与Nrf2基因缺失的小鼠杂交可逆转Keap1基因缺失的表型。这些实验表明,在细胞对氧化和外源性应激的反应中,Keap1在Nrf2的上游起作用。

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