...
首页> 外文期刊>Integrative Biosciences >Analysis of the Caenorhabditis elegans dlk-1 Gene Expression
【24h】

Analysis of the Caenorhabditis elegans dlk-1 Gene Expression

机译:秀丽隐杆线虫dlk-1基因表达分析

获取原文
获取原文并翻译 | 示例
           

摘要

C. elegans DLK-1 has been reported to play an important role in synaptogenesis by shaping the structure of presynaptic terminal. In this study, we investigated the expression pattern and regulation of the dlk-1 gene in C. elegans. To determine the expression pattern, we made a dlk-1::gfp fusion construct, named pPDdg1, which consisted of approx 2.2 kb 5' upstream region, the first exon, the first intron, and a part of the second exon of the dlk-1 gene. By microinjecting this construct into the worm,we observed that the DLK-1::GFP was expressed mainly in neurons. We next examined the regulatory elements of gene expression by deletion analysis of pPDdg1. Removal of a large portion of the 5' upstream region (delta-361 to -2246) of the gene had littleeffect on the expression pattern, whereas deletion of the first intron led to elimination of the DLK-1::GFP expression in most of the neurons. Our results suggest that the first intron of the C. elegans dlk-1 gene contains the regulatory element criticalfor gene expression.
机译:秀丽隐杆线虫DLK-1已被报道通过塑造突触前末端的结构在突触发生中起重要作用。在这项研究中,我们调查了线虫中dlk-1基因的表达模式和调控。为了确定表达模式,我们制作了一个名为pPDdg1的dlk-1 :: gfp融合构建体,它由大约2.2 kb 5'上游区域,第一个外显子,第一个内含子和dlk的第二个外显子组成。 -1基因。通过将该构建体显微注射到蠕虫中,我们观察到DLK-1 :: GFP主要在神经元中表达。接下来,我们通过pPDdg1的缺失分析检查了基因表达的调控元件。去除基因的5'上游区域的大部分(δ-361至-2246)对表达模式几乎没有影响,而删除第一个内含子则导致大部分DLK-1 :: GFP表达的消除。神经元。我们的结果表明,秀丽隐杆线虫dlk-1基因的第一个内含子包含对基因表达至关重要的调控元件。

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