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Prep1,一种参与葡萄糖和脂质代谢的同源结构域转录因子。

Prep1, A Homeodomain Transcription Factor Involved in Glucose and Lipid Metabolism.

作者信息

Oriente Francesco, Perruolo Giuseppe, Cimmino Ilaria, Cabaro Serena, Liotti Antonietta, Longo Michele, Miele Claudia, Formisano Pietro, Beguinot Francesco

机构信息

Department of Translational Medicine, Federico II University of Naples, Naples, Italy.

URT Genomic of Diabetes, Institute of Experimental Endocrinology and Oncology, National Research Council, Naples, Italy.

出版信息

Front Endocrinol (Lausanne). 2018 Jun 28;9:346. doi: 10.3389/fendo.2018.00346. eCollection 2018.

Abstract

The three-amino acid loop extension (TALE) homeodomain proteins are a family of transcription factor including the mammalian Pbx, MEIS and Prep proteins. TALE proteins can bind other transcription factors such as Pdx-1 and play an important role in the regulation of glucose metabolism. Experiments performed in mutant mice have shown that while the single or knockout mice feature pancreatic islet malformations, impaired glucose tolerance and hypoinsulinemia, the trans-heterozygous mice develop age-dependent overt diabetes mellitus. In contrast, Prep1 plays a different role with respect to these proteins. Indeed, hypomorphic mice, expressing low levels of protein, feature pancreatic islet hypoplasia accompanied by hypoinsulinemia similar to Pbx1 or Pdx1. Nevertheless, these animals show increased insulin sensitivity in skeletal muscle, liver and adipose tissue accompanied by protection from streptozotocin-induced diabetes. In addition, hypomorphic mice feature reduced triglyceride synthesis and do not develop steatohepatitis after a methionine and coline deficient diet. In this review we have underlined how important metabolic functions are controlled by TALE proteins, in particular by Prep1, leading to hypothesis that its suppression might represent beneficial effect in the care of metabolic diseases.

摘要

三氨基酸环延伸(TALE)同源结构域蛋白是一类转录因子,包括哺乳动物的Pbx、MEIS和Prep蛋白。TALE蛋白可与其他转录因子如Pdx-1结合,并在葡萄糖代谢调节中发挥重要作用。在突变小鼠中进行的实验表明,虽然单基因敲除或基因敲除小鼠存在胰岛畸形、糖耐量受损和低胰岛素血症,但反式杂合小鼠会发展为年龄依赖性显性糖尿病。相比之下,Prep1在这些蛋白方面发挥着不同的作用。实际上,表达低水平蛋白的次等位基因突变小鼠表现出胰岛发育不全,并伴有与Pbx1或Pdx1相似的低胰岛素血症。然而,这些动物在骨骼肌、肝脏和脂肪组织中表现出胰岛素敏感性增加,并对链脲佐菌素诱导的糖尿病具有保护作用。此外,次等位基因突变小鼠的甘油三酯合成减少,在蛋氨酸和胆碱缺乏饮食后不会发生脂肪性肝炎。在本综述中,我们强调了TALE蛋白,特别是Prep1对代谢功能的控制有多重要,由此提出其抑制作用可能对代谢疾病的治疗具有有益效果的假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/6032887/9cf1755d2339/fendo-09-00346-g0001.jpg

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