首页> 美国卫生研究院文献>Molecular and Cellular Biology >Housekeeping NaK-ATPase alpha 1 subunit gene promoter is composed of multiple cis elements to which common and cell type-specific factors bind.
【2h】

Housekeeping NaK-ATPase alpha 1 subunit gene promoter is composed of multiple cis elements to which common and cell type-specific factors bind.

机译:管家NaK-ATPaseα1亚基基因启动子由多个顺式元件组成这些顺式元件与常见和细胞类型特异性因子结合。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Na,K-ATPase alpha 1 subunit gene (ATP1A1) is one of the housekeeping genes involved in homeostasis of Na+ and K+ in all animal cells. We identified and characterized the cis-acting elements that regulate the expression of ATP1A1. The region between -155 and -49 was determined as a positive regulatory region in five cultured cell lines of different tissue origins (MDCK, B103, L6, 3Y1, and HepG2). The region was divided into three subregions: from -120 to -106 (including the Sp1 binding site), from -102 to -61, and from -58 to -49 (including an Sp1 consensus sequence). Cell type-specific factors binding to the middle subregion (from -102 to -61) were detected by gel retardation analysis, using nuclear extracts prepared from MDCK and B103 cells. Two gel retardation complexes were formed in the B103 nuclear extract, and three were formed in the MDCK nuclear extract. DNA binding regions of these factors were located at -88 to -69 and differed from each other in DNase I footprinting experiments. These factors also showed different binding characteristics in gel retardation competition and methylation interference experiments. The identified cis element was named the ATP1A1 regulatory element. The core sequence of this element is found in several other genes involved in cellular energy metabolism, suggesting that the sequence is a common regulatory element responsive to the state of energy metabolism.
机译:Na,K-ATPaseα1亚基基因(ATP1A1)是参与所有动物细胞Na +和K +体内平衡的管家基因之一。我们鉴定并表征了调节ATP1A1表达的顺式作用元件。在-155和-49之间的区域被确定为来自不同组织起源的五种培养细胞系(MDCK,B103,L6、3Y1和HepG2)中的阳性调控区域。该区域分为三个子区域:-120至-106(包括Sp1结合位点),-102至-61和-58至-49(包括Sp1共有序列)。使用从MDCK和B103细胞制备的核提取物,通过凝胶阻滞分析检测结合到中间子区域(-102至-61)的细胞类型特异性因子。在B103核提取物中形成了两个凝胶延迟复合物,在MDCK核提取物中形成了三个凝胶延迟复合物。这些因子的DNA结合区域位于-88至-69之间,在DNase I足迹实验中彼此不同。这些因素在凝胶延迟竞争和甲基化干扰实验中也显示出不同的结合特性。鉴定出的顺式元件称为ATP1A1调节元件。该元素的核心序列存在于参与细胞能量代谢的其他几个基因中,这表明该序列是对能量代谢状态做出反应的常见调控元件。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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