Department of Neurobiology and Anatomy, University of Utah School of Medicine, Salt Lake City, Utah 84132-3401, USA.
Dev Dyn. 2011 Jun;240(6):1537-47. doi: 10.1002/dvdy.22616. Epub 2011 Apr 4.
We have developed "b" and "c" isoform-specific chicken fibroblast growth factor (FGF) receptor 1-3 probes for in situ hybridization. We rigorously demonstrate the specificity of these probes by using both dot blot hybridization and whole-mount in situ hybridization during neurulation and early postneurulation stages, and we compare expression patterns of each of the three isoform-specific probes to one another and to generic probes to each of the three (non-isoform-specific) FGF receptors. We show that the expression pattern of each receptor is represented by the collective expression of each of its two isoforms, with the expression of each FGF receptor being most similar to that of its "c" isoform at two of the three stages studied, and that tissue and stage differences exist in the patterns of expression of the six isoforms. We demonstrate the usefulness of these probes for defining the differential tissue expression of FGF receptor 1-3 isoforms.
我们开发了“b”和“c”同工型特异性鸡成纤维细胞生长因子(FGF)受体 1-3 探针,用于原位杂交。我们通过在神经胚形成和早期神经胚形成阶段使用斑点印迹杂交和整体原位杂交,严格证明了这些探针的特异性,并将三种同工型特异性探针中的每一种的表达模式彼此进行比较,并与每种(非同工型特异性)FGF 受体的通用探针进行比较。我们表明,每个受体的表达模式由其两个同工型中的每一个的集体表达来表示,在研究的三个阶段中的两个阶段,每个 FGF 受体的表达与它的“c”同工型最相似,并且在六种同工型的表达模式中存在组织和阶段差异。我们证明了这些探针对于定义 FGF 受体 1-3 同工型的组织差异表达的有用性。