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Forkhead Box Transcription Factors of the FOXA Class Are Required for Basal Transcription of Angiotensin-Converting Enzyme 2

机译:血管紧张素转换酶2的基础转录需要FOXA类的前叉框转录因子。

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摘要

Angiotensin-converting enzyme 2 (ACE2) has protective effects on a wide range of morbidities associated with elevated angiotensin-II signaling. Most tissues, including pancreatic islets, express ACE2 mainly from the proximal promoter region. We previously found that hepatocyte nuclear factors 1α and 1β stimulate ACE2 expression from three highly conserved hepatocyte nuclear factor 1 binding motifs in the proximal promoter region. We hypothesized that other highly conserved motifs would also affect ACE2 expression. By systematic mutation of conserved elements, we identified five regions affecting ACE2 expression, of which two regions bound transcriptional activators. One of these is a functional FOXA binding motif. We further identified the main protein binding the FOXA motif in 832/13 insulinoma cells as well as in mouse pancreatic islets as FOXA2.
机译:血管紧张素转换酶2(ACE2)对与血管紧张素II信号转导升高相关的多种疾病具有保护作用。大多数组织,包括胰岛,主要从近端启动子区域表达ACE2。我们先前发现,肝细胞核因子1α和1β从近端启动子区域的三个高度保守的肝细胞核因子1结合基序中刺激ACE2表达。我们假设其他高度保守的基序也会影响ACE2的表达。通过保守元件的系统突变,我们确定了影响ACE2表达的五个区域,其中两个区域结合了转录激活因子。其中之一是功能性FOXA结合基序。我们进一步确定了832/13胰岛素瘤细胞以及小鼠胰岛中与FOXA2结合的FOXA基序的主要蛋白质。

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