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通过原位杂交对肢体发育过程中软骨蛋白聚糖核心蛋白基因表达进行时空分析。

Temporal and spatial analysis of cartilage proteoglycan core protein gene expression during limb development by in situ hybridization.

作者信息

Mallein-Gerin F, Kosher R A, Upholt W B, Tanzer M L

机构信息

Department of BioStructure, University of Connecticut Health Center, Farmington 06032.

出版信息

Dev Biol. 1988 Apr;126(2):337-45. doi: 10.1016/0012-1606(88)90144-3.

Abstract

As limb mesenchymal cells differentiate into chondrocytes they initiate the synthesis of a cartilage-specific sulfated proteoglycan, cartilage-characteristic type II collagen, and other cartilage-specific proteins. In the present study, in situ hybridization with a 32P-labeled cloned cDNA probe complementary to mRNA encoding the core protein of cartilage proteoglycan has been used to visualize and localize the accumulation of cartilage proteoglycan core protein mRNA sequences during development of the chick limb bud in vivo. When the probe was hybridized to sections through 7-day (stage 32) limbs, an intense hybridization signal was observed over the well-differentiated cartilage rudiments of the limb, while no signal above background was observed over nonchondrogenic tissues including muscle, loose connective tissue, and epidermis. At early stages of limb development, an accumulation of silver grains representing hybridizable core protein mRNA first became detectable in the proximal central core of the limb where the prechondrogenic condensation of mesenchymal cells that characterizes the onset of cartilage differentiation was occurring. In fact, the pattern of silver grain accumulation closely followed the pattern of mesenchymal cell condensation, and no hybridizable core protein mRNA sequences were detectable in the limb bud prior to condensation. Cartilage-characteristic type II collagen mRNA was colocalized with core protein mRNA in the condensing central core of the limb suggesting that the genes for these two major constituents of cartilage matrix are coordinately regulated at the onset of chondrogenesis. Furthermore, the appearance of hybridizable core protein mRNA was closely followed by the appearance of the protein for which it codes as detected by immunohistochemical staining with monospecific antibody. These observations support the hypothesis that at the initial stages of limb chondrogenesis core protein gene expression is controlled primarily at the transcriptional level.

摘要

当肢体间充质细胞分化为软骨细胞时,它们开始合成一种软骨特异性硫酸化蛋白聚糖、软骨特征性II型胶原以及其他软骨特异性蛋白。在本研究中,已使用与编码软骨蛋白聚糖核心蛋白的mRNA互补的32P标记克隆cDNA探针进行原位杂交,以在体内鸡肢体芽发育过程中可视化并定位软骨蛋白聚糖核心蛋白mRNA序列的积累。当该探针与7天(第32阶段)肢体的切片杂交时,在肢体分化良好的软骨原基上观察到强烈的杂交信号,而在包括肌肉、疏松结缔组织和表皮在内的非软骨形成组织上未观察到高于背景的信号。在肢体发育的早期阶段,代表可杂交核心蛋白mRNA的银颗粒积累首先在肢体近端中央核心中检测到,此处正在发生间充质细胞的软骨前凝聚,这是软骨分化开始的特征。事实上,银颗粒积累模式紧密跟随间充质细胞凝聚模式,并且在凝聚之前的肢体芽中未检测到可杂交的核心蛋白mRNA序列。软骨特征性II型胶原mRNA与核心蛋白mRNA在肢体凝聚的中央核心中共定位,表明软骨基质这两种主要成分的基因在软骨形成开始时受到协调调节。此外,可杂交核心蛋白mRNA出现后不久,通过单特异性抗体免疫组织化学染色检测到其编码的蛋白质也出现了。这些观察结果支持这样的假设,即在肢体软骨形成的初始阶段,核心蛋白基因表达主要在转录水平受到控制。

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