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小鼠μ阿片受体基因启动子序列的基因组结构分析

Genomic structure analysis of promoter sequence of a mouse mu opioid receptor gene.

作者信息

Min B H, Augustin L B, Felsheim R F, Fuchs J A, Loh H H

机构信息

Department of Pharmacology, University of Minnesota, Minneapolis 55455.

出版信息

Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9081-5. doi: 10.1073/pnas.91.19.9081.

Abstract

We have isolated mouse mu opioid receptor genomic clones (termed MOR) containing the entire amino acid coding sequence corresponding to rat MOR-1 cDNA, including additional 5' flanking sequence. The mouse MOR gene is > 53 kb long, and the coding sequence is divided by three introns, with exon junctions in codons 95 and 213 and between codons 386 and 387. The first intron is > 26 kb, the second is 0.8 kb, and the third is > 12 kb. Multiple transcription initiation sites were observed, with four major sites confirmed by 5' rapid amplification of cDNA ends and RNase protection located between 291 and 268 bp upstream of the translation start codon. Comparison of the 5' flanking sequence with a transcription factor database revealed putative cis-acting regulatory elements for transcription factors affected by cAMP, as well as those involved in the action of gluco- and mineralocorticoids, cytokines, and immune-cell-specific factors.

摘要

我们分离出了小鼠μ阿片受体基因组克隆(称为MOR),其包含与大鼠MOR-1 cDNA相对应的完整氨基酸编码序列,包括额外的5'侧翼序列。小鼠MOR基因长度超过53 kb,编码序列被三个内含子分隔,外显子连接位于密码子95和213以及密码子386和387之间。第一个内含子超过26 kb,第二个为0.8 kb,第三个超过12 kb。观察到多个转录起始位点,通过5' cDNA末端快速扩增和核糖核酸酶保护确定了四个主要位点,位于翻译起始密码子上游291至268 bp之间。将5'侧翼序列与转录因子数据库进行比较,发现了受cAMP影响的转录因子以及参与糖皮质激素、盐皮质激素、细胞因子和免疫细胞特异性因子作用的假定顺式作用调控元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f59d/44751/ad95dbeaf704/pnas01141-0365-a.jpg

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