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三种小鼠甲胎蛋白基因增强子的精细结构图谱

Fine-structure mapping of the three mouse alpha-fetoprotein gene enhancers.

作者信息

Godbout R, Ingram R S, Tilghman S M

机构信息

Lewis Thomas Laboratory, Department of Molecular Biology, Princeton University, New Jersey 08544.

出版信息

Mol Cell Biol. 1988 Mar;8(3):1169-78. doi: 10.1128/mcb.8.3.1169-1178.1988.

DOI:10.1128/mcb.8.3.1169-1178.1988
PMID:2452972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC363261/
Abstract

Multiple cellular enhancers have been identified previously in the 5'-flanking region of the mouse alpha-fetoprotein gene by transient expression assay. In this report the enhancers have been localized to three regions 200 to 300 base pairs in length at 2.5, 5.0, and 6.5 kilobases of DNA upstream of the transcriptional start site. Nucleotide sequence analysis of the three enhancers revealed areas of homology among them, the most significant of which were two regions of 10 and 18 nucleotides in length. Two of the enhancers were analyzed in detail and shown to be composed of multiple nonidentical domains, none of which was sufficient for full enhancer activity; rather, they acted in an additive fashion in generating the full activity of the enhancer. The tissue-specific activity of the enhancer at -2.5 kilobases was assessed by comparing the activities of subdomains in liver- and non-liver-derived cell lines and was found to be the result of both positive elements within the enhancer and at least one negative element to its 5' end. In contrast, the tissue specificity of the enhancer at -5.0 kilobases was maintained when the minimal essential region was tested alone. The nucleotide sequence similarities, as well as the differences among the enhancers, may explain their differing biological activities both in tissue culture and in vivo.

摘要

先前通过瞬时表达分析已在小鼠甲胎蛋白基因的5'侧翼区域鉴定出多个细胞增强子。在本报告中,这些增强子已定位到转录起始位点上游2.5、5.0和6.5千碱基处三个长度为200至300个碱基对的区域。对这三个增强子的核苷酸序列分析揭示了它们之间的同源区域,其中最显著的是两个长度分别为10和18个核苷酸的区域。对其中两个增强子进行了详细分析,结果表明它们由多个不同的结构域组成,其中没有一个结构域足以产生完整的增强子活性;相反,它们以累加的方式发挥作用以产生增强子的全部活性。通过比较肝源性和非肝源性细胞系中亚结构域的活性,评估了-2.5千碱基处增强子的组织特异性活性,发现这是增强子内的正向元件及其5'端至少一个负向元件共同作用的结果。相比之下,单独测试最小必需区域时,-5.0千碱基处增强子的组织特异性得以维持。增强子之间的核苷酸序列相似性以及差异,可能解释了它们在组织培养和体内不同的生物学活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f1/363261/44ff6f9df677/molcellb00063-0174-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f1/363261/cf142a4bfec1/molcellb00063-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f1/363261/44ff6f9df677/molcellb00063-0174-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f1/363261/cf142a4bfec1/molcellb00063-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f1/363261/44ff6f9df677/molcellb00063-0174-a.jpg

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本文引用的文献

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