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α1(I)型胶原基因的第一个内含子包含多个转录调控元件。

The first intron of the alpha 1(I) collagen gene contains several transcriptional regulatory elements.

作者信息

Bornstein P, McKay J

机构信息

Department of Biochemistry, University of Washington, Seattle 98195.

出版信息

J Biol Chem. 1988 Feb 5;263(4):1603-6.

PMID:2828347
Abstract

The first intron of the human alpha 1(I) collagen gene contains a negatively acting element that inhibits transcription of the chloramphenicol acetyltransferase gene driven by either a collagen or an SV40 basal promoter (Bornstein, P., McKay, J., Morishima, J., Devarayalu, S., and Gelinas, R. E. (1987) Proc. Natl. Acad. Sci. U. S. A. 84, in press). We now find that this element is flanked by sequences that both neutralize the inhibitory effect and impart a net positive effect on transcription. A collagen-human growth hormone minigene was constructed in which varying lengths of the collagen intron were retained. Plasmids were transfected into chick tendon fibroblasts, and transcriptional activity was measured by solution hybridization with an antisense RNA probe. The presence of the intact intronic sequence stimulated transcription by a factor of 2-3-fold in comparison with intron-deleted plasmids. However, the isolated negatively acting element inhibited transcription by a factor of 15-20-fold. Surprisingly, this effect was markedly orientation-dependent. Intronic segments flanking the negatively acting element stimulated transcription both when cloned 5' to the collagen promoter in chloramphenicol acetyltransferase-based plasmids and 3' in collagen-human growth hormone constructions. We conclude that expression of the alpha 1(I) collagen gene is controlled by several intronic elements that function coordinately with 5'-flanking and promoter elements.

摘要

人类α1(I)型胶原基因的第一个内含子含有一个负性作用元件,该元件可抑制由胶原或SV40基础启动子驱动的氯霉素乙酰转移酶基因的转录(伯恩斯坦,P.,麦凯,J.,森岛,J.,德瓦拉亚卢,S.,和盖利纳斯,R.E.(1987年)《美国国家科学院院刊》84卷,即将发表)。我们现在发现,该元件两侧的序列既能中和抑制作用,又能对转录产生净正向作用。构建了一个胶原-人生长激素微型基因,其中保留了不同长度的胶原内含子。将质粒转染到鸡肌腱成纤维细胞中,并通过与反义RNA探针的溶液杂交来测量转录活性。与缺失内含子的质粒相比,完整内含子序列的存在使转录增强了2至3倍。然而,分离出的负性作用元件却使转录抑制了15至20倍。令人惊讶的是,这种效应明显依赖于方向。负性作用元件两侧的内含子片段,无论是克隆到基于氯霉素乙酰转移酶的质粒中胶原启动子的5'端,还是克隆到胶原-人生长激素构建体的3'端,均能刺激转录。我们得出结论,α1(I)型胶原基因的表达受几个内含子元件的控制,这些元件与5'侧翼元件和启动子元件协同发挥作用。

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