Shames R B, Knapp L W, Carver W E, Sawyer R H
Department of Biology, University of South Carolina, Columbia 29208.
Differentiation. 1988 Jul;38(2):115-23. doi: 10.1111/j.1432-0436.1988.tb00205.x.
Epidermal-dermal interactions influence morphogenesis and expression of the beta keratin gene family during development of scales in the embryonic chick. The underlying mechanisms by which these interactions control beta keratin expression are not understood. However, the present study of beta keratin gene expression during avian epidermal differentiation contributes new information with which to investigate the role of tissue interactions in this process. Using beta keratin-specific synthetic oligonucleotide probe, beta keratin mRNA was hybrid-selected from total poly A+ RNA of scutate scales. Seven beta keratin polypeptides were translated in vitro and could be identified by their positions in two-dimensional gels among the detergent-insoluble extracts of scutate scale epidermis. In vivo phosphorylation studies suggested that an additional three beta keratin polypeptides were present as phosphoproteins. The temporal appearance of beta keratin mRNA and the corresponding polypeptides was followed during scutate scale development. Polyclonal antiserum made against two of the beta keratin polypeptides was used for immunohistochemical and immunogold electron-microscopic analysis of beta keratin tissue distribution. Immunological reactivity was observed specifically along the outer scale surface in epidermal cells above the stratum germinativum. Immunogold beads were localized on 3-nm filament bundles. In situ hybridization with a beta keratin-specific RNA probe demonstrated that mRNA accumulated in the same regional manner as the polypeptides. This selective expression of beta keratin genes in specific regions of the developing scutate scale suggests that epidermal-dermal interactions provide not only for morphological events, but also for control of complex patterns of histogenesis and biochemical differentiation.
在鸡胚鳞片发育过程中,表皮 - 真皮相互作用影响β角蛋白基因家族的形态发生和表达。这些相互作用控制β角蛋白表达的潜在机制尚不清楚。然而,目前对鸟类表皮分化过程中β角蛋白基因表达的研究为探究组织相互作用在此过程中的作用提供了新信息。使用β角蛋白特异性合成寡核苷酸探针,从盾形鳞片的总聚腺苷酸 + RNA中杂交选择β角蛋白mRNA。七种β角蛋白多肽在体外进行翻译,并可通过其在盾形鳞片表皮去垢剂不溶性提取物的二维凝胶中的位置来鉴定。体内磷酸化研究表明,另外三种β角蛋白多肽以磷蛋白形式存在。在盾形鳞片发育过程中追踪β角蛋白mRNA和相应多肽的出现时间。针对其中两种β角蛋白多肽制备的多克隆抗血清用于β角蛋白组织分布的免疫组织化学和免疫金电子显微镜分析。在生发层上方的表皮细胞中,在外鳞片表面特异性观察到免疫反应性。免疫金珠定位于3纳米细丝束上。用β角蛋白特异性RNA探针进行原位杂交表明,mRNA以与多肽相同的区域方式积累。β角蛋白基因在发育中的盾形鳞片特定区域的这种选择性表达表明,表皮 - 真皮相互作用不仅为形态学事件提供条件,而且还控制组织发生和生化分化的复杂模式。