首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Two CCAAT boxes in a novel inverted repeat motif are required for Hlx homeobox gene expression
【24h】

Two CCAAT boxes in a novel inverted repeat motif are required for Hlx homeobox gene expression

机译:Hlx同源框基因表达需要两个具有新颖反向重复基序的CCAAT框

获取原文
获取原文并翻译 | 示例
       

摘要

Hlx is a homeobox transcription factor gene required for normal intestinal and hepatic growth in development. We previously found high sequence identity and 17 conserved consensus cis-regulatory/transcription factor binding elements in the mouse and human Hlx 5' regions. A 594 sequence in the Hlx 5' region possessing the same activity in driving luciferase expression as larger Hlx 5' sequences had three segments each necessary but not sufficient for luciferase expression in NIH 3T3 cells (which express Hlx). Nine of the conserved putative regulatory elements are positioned within these segments, including two CCAAT boxes on opposite strands within a conserved 44 bp inverted repeat sequence. To test the hypothesis that these elements are required for promoter activity, we compared the reporter expression activity of segments containing mutations of these elements with activity of the parent Hlx promoter sequence. We found that mutation of either CCAAT box or a conserved AP-2 site resulted in a significant decrease in promoter activity. Restoration of the inverted repeat with complementary mutations of both CCAAT boxes did not restore activity. Further, mutation of other portions of the inverted repeat did not affect promoter activity. Mutation of other elements had no effect on promoter activity.
机译:Hlx是正常肠道和肝脏发育所必需的同源盒转录因子基因。我们先前在小鼠和人类Hxx 5'区发现了高序列同一性和17个保守的顺式-调控/转录因子结合元件。 Hlx 5'区域中的594序列在驱动萤光素酶表达方面具有相同的活性,而较大的Hlx 5'序列具有三个片段,每个片段对于在NIH 3T3细胞(表达Hlx)中的萤光素酶表达而言都是必需的,但不足。九个保守的推定调控元件位于这些区段内,包括在保守的44 bp反向重复序列内相对链上的两个CCAAT盒。为了检验这些元件是启动子活性所必需的假设,我们将含有这些元件突变的区段的报道基因表达活性与亲本H1x启动子序列的活性进行了比较。我们发现,CCAAT框或保守的AP-2位点的突变导致启动子活性显着下降。用两个CCAAT盒的互补突变恢复反向重复序列均不能恢复活性。此外,反向重复的其他部分的突变不影响启动子活性。其他元件的突变对启动子活性没有影响。

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