Suppr超能文献

小鼠α2(XI)胶原蛋白启动子中软骨和神经组织特异性顺式元件的模块化排列。

Modular arrangement of cartilage- and neural tissue-specific cis-elements in the mouse alpha2(XI) collagen promoter.

作者信息

Tsumaki N, Kimura T, Tanaka K, Kimura J H, Ochi T, Yamada Y

机构信息

Department of Orthopaedic Surgery, Osaka University Medical School, Suita 565-0871, Japan.

出版信息

J Biol Chem. 1998 Sep 4;273(36):22861-4. doi: 10.1074/jbc.273.36.22861.

Abstract

Type XI collagen, a heterotrimer specific to cartilage matrix, plays an important role in cartilage morphogenesis. We analyzed various alpha2(XI) collagen promoter-lacZ reporter gene constructs in transgenic mice to understand tissue-specific transcriptional regulation. The -530 promoter sequence was sufficient to direct reporter gene expression specifically to cartilage. Further deletion to -500 abolished reporter gene expression in cartilage but activated the expression specific to neural tissues such as brain and neural tube. An additional 47-base pair deletion resulted in random tissue expression patterns. A 24-base pair sequence from -530 to -507 of the alpha2(XI) promoter was able to switch the activity of the heterologous neurofilament light gene promoter from neural tissues to cartilage. These results suggest that the alpha2(XI) collagen gene is regulated by at least three modular elements: a basal promoter sequence distal to -453, a neural tissue-specific element (-454 to -500), and a cartilage-specific element (-501 to -530), which inhibits expression in neural tissues and induces expression in cartilage.

摘要

XI型胶原蛋白是软骨基质特有的异源三聚体,在软骨形态发生中起重要作用。我们在转基因小鼠中分析了各种α2(XI)胶原蛋白启动子-lacZ报告基因构建体,以了解组织特异性转录调控。-530启动子序列足以将报告基因的表达特异性地导向软骨。进一步缺失至-500消除了软骨中的报告基因表达,但激活了大脑和神经管等神经组织特异性的表达。额外缺失47个碱基对导致随机的组织表达模式。α2(XI)启动子从-530到-507的24个碱基对序列能够将异源神经丝轻基因启动子的活性从神经组织切换到软骨。这些结果表明,α2(XI)胶原蛋白基因受至少三个模块化元件调控:-453远端的基础启动子序列、神经组织特异性元件(-454至-500)和软骨特异性元件(-501至-530),后者抑制神经组织中的表达并诱导软骨中的表达。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验