...
首页> 外文期刊>Molecular and Cellular Biochemistry >Molecular cloning and expression of chicken carbohydrate response element binding protein and Max-like protein X gene homologues
【24h】

Molecular cloning and expression of chicken carbohydrate response element binding protein and Max-like protein X gene homologues

机译:鸡碳水化合物反应元件结合蛋白和Max样蛋白X基因同源物的分子克隆与表达

获取原文
获取原文并翻译 | 示例

摘要

Carbohydrate response element binding protein (ChREBP) and sterol regulatory element binding protein-1c (SREBP-1c) are transcription factors that are known to be key regulators of glucose metabolism and lipid synthesis in mammals. Since ChREBP and its co-activator Max-like protein X (Mlx) have not been identified in birds, the objectives of this work were to clone, sequence, and characterize the genomic organization of ChREBP and Mlx genes and to determine the expression of ChREBP, Mlx, and several related genes including liver X receptor (LXR), SREBP-1 and thyroid hormone responsive Spot 14 (Spot 14) in chickens. Alternative splicing resulted in two ChREBP mRNA transcript variants that code for predicted proteins of 895 and 869 amino acids. The chicken Mlx gene produced a single mRNA transcript that codes for a predicted protein of 245 amino acids. Chicken ChREBP and Mlx predicted proteins shared high amino acid homology with select portions of corresponding mammalian proteins. In chickens, Mlx, SREBP-1, and LXR were expressed at comparable levels in all tissues examined. However, ChREBP demonstrated significant tissue-specific expression with the highest mRNA levels found in liver and duodenum and Spot 14 was expressed predominantly in liver and abdominal fat. Using Western blotting, the presence of ChREBP protein was detected in chicken liver tissue. Our findings add new insight into a potential role for specific transcription factors such as ChREBP and Mlx in the glucose-dependent regulation of lipogenesis in birds.
机译:碳水化合物反应元件结合蛋白(ChREBP)和固醇调节元件结合蛋白1c(SREBP-1c)是转录因子,已知是哺乳动物葡萄糖代谢和脂质合成的关键调节剂。由于尚未在鸟类中鉴定出ChREBP及其共激活因子Max样蛋白X(Mlx),因此这项工作的目的是克隆,测序和表征ChREBP和Mlx基因的基因组组织,并确定ChREBP的表达。 ,Mlx和几种相关基因,包括鸡的肝X受体(LXR),SREBP-1和甲状腺激素反应性斑点14(斑点14)。选择性剪接导致两个ChREBP mRNA转录变体,编码895和869个氨基酸的预测蛋白。鸡的Mlx基因产生单个mRNA转录本,编码245个氨基酸的预测蛋白。鸡ChREBP和Mlx预测的蛋白质与相应哺乳动物蛋白质的选定部分具有较高的氨基酸同源性。在鸡中,Mlx,SREBP-1和LXR在所有检查的组织中均以可比较的水平表达。然而,ChREBP表现出明显的组织特异性表达,在肝脏和十二指肠中具有最高的mRNA水平,而Spot 14主要在肝脏和腹部脂肪中表达。使用蛋白质印迹法,在鸡肝组织中检测到ChREBP蛋白的存在。我们的发现为特定转录因子(例如ChREBP和Mlx)在鸟类脂肪形成的葡萄糖依赖性调节中的潜在作用提供了新的见解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号