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Egr-1(一种小鼠丝裂原诱导的锌指编码基因)的5'侧翼序列和基因组结构

5' flanking sequence and genomic structure of Egr-1, a murine mitogen inducible zinc finger encoding gene.

作者信息

Tsai-Morris C H, Cao X M, Sukhatme V P

机构信息

Department of Medicine, Howard Hughes Medical Institute, University of Chicago, IL 60637.

出版信息

Nucleic Acids Res. 1988 Sep 26;16(18):8835-46. doi: 10.1093/nar/16.18.8835.

Abstract

Egr-1 is a murine zinc finger encoding cDNA whose expression is modulated by a variety of ligand-receptor interactions and is often coregulated with c-fos (1). This study reports the isolation of a mouse Egr-1 genomic clone, its intron-exon structure, and 935 bp of 5' flanking sequence. The gene spans about 3.8 kb and consists of 2 exons and one 700 bp intron. S1 nuclease protection and primer extension analysis were used to define the transcription initiation site. "TATA" and "CCAAT" sequences were located at nucleotides -26 and -337 respectively. In addition, there exist five elements whose sequence is nearly identical to the inner core 10 nucleotide region (CCATATTAGG) of the c-fos serum response element, four Sp1 consensus sequences, two AP1 target sequence analogs, and two potential cAMP response elements. These results will ultimately lead to a detailed definition of the intracellular events regulating Egr-1 expression.

摘要

Egr-1是一种编码cDNA的鼠类锌指蛋白,其表达受多种配体-受体相互作用的调节,且常与c-fos共同调节(1)。本研究报告了小鼠Egr-1基因组克隆的分离、其内含子-外显子结构以及935 bp的5'侧翼序列。该基因跨度约3.8 kb,由2个外显子和一个700 bp的内含子组成。使用S1核酸酶保护和引物延伸分析来确定转录起始位点。“TATA”和“CCAAT”序列分别位于核苷酸-26和-337处。此外,存在五个与c-fos血清反应元件的内核10核苷酸区域(CCATATTAGG)序列几乎相同的元件、四个Sp1共有序列、两个AP1靶序列类似物以及两个潜在的cAMP反应元件。这些结果最终将导致对调节Egr-1表达的细胞内事件的详细定义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd5a/338638/dd1d39db316d/nar00160-0095-a.jpg

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