Galili N, Epstein J A, Leconte I, Nayak S, Buck C A
The Wistar Institute, Philadelphia, Pennsylvania 19104, USA.
Dev Dyn. 1998 May;212(1):86-93. doi: 10.1002/(SICI)1097-0177(199805)212:1<86::AID-AJA8>3.0.CO;2-Z.
Gscl, a paired-type homeobox gene, has been implicated in the pathology of DGS/VCFS by virtue of its genomic location and its structural similarity to the Gsc gene family. Immunohistochemical and in situ studies were performed to examine the expression pattern of this gene during embryonic development. A polyclonal antibody, generated to the full-length protein and shown to be specific for GSCL by both Western blotting and immunofluorescence, was used for immunohistochemical localization. Both in situ and antibody staining localized GSCL expression to a cluster of cells in the pons region of the developing brain. This GSCL expression pattern showed partial overlap with that of Pax6. More detailed immunohistochemistry revealed the GSCL in primordial germ cells during migration from the epithelium of the hindgut and later as they colonize the developing gonads. GSCL was not detected in tissues affected in DGS/VCSF.
Gscl是一种配对型同源框基因,因其基因组位置以及与Gsc基因家族的结构相似性,被认为与22q11.2缺失综合征/腭心面综合征的病理机制有关。进行了免疫组织化学和原位研究,以检测该基因在胚胎发育过程中的表达模式。使用针对全长蛋白产生的多克隆抗体,通过蛋白质免疫印迹和免疫荧光显示其对GSCL具有特异性,用于免疫组织化学定位。原位和抗体染色均将GSCL表达定位到发育中大脑脑桥区域的一群细胞。这种GSCL表达模式与Pax6的表达模式部分重叠。更详细的免疫组织化学显示,在原始生殖细胞从后肠上皮迁移过程中以及后来它们定殖到发育中的性腺时,存在GSCL。在22q11.2缺失综合征/腭心面综合征所累及的组织中未检测到GSCL。