Samad Tarek A, Srinivasan Ashok, Karchewski Laurie A, Jeong Sung-Jin, Campagna Jason A, Ji Ru-Rong, Fabrizio David A, Zhang Ying, Lin Herbert Y, Bell Esther, Woolf Clifford J
Neural Plasticity Research Group, Department of Anesthesia and Critical Care, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02129, USA.
J Neurosci. 2004 Feb 25;24(8):2027-36. doi: 10.1523/JNEUROSCI.4115-03.2004.
DRG11, a transcription factor expressed in embryonic dorsal root ganglion (DRG) and dorsal horn neurons, has a role in the development of sensory circuits. We have used a genomic binding strategy to screen for the promoter region of genes regulated by DRG11. One gene with a promoter region binding to the DNA binding domain of DRG11 encodes a novel membrane-associated [glycosyl-phosphatidylinositol (GPI)-anchored] protein that we call DRAGON. DRAGON expression is transcriptionally regulated by DRG11, and it is coexpressed with DRG11 in embryonic DRG and spinal cord. DRAGON expression in these areas is reduced in DRG11 null mutants. DRAGON is expressed, however, in the neural tube before DRG11, and unlike DRG11 it is expressed in the brain and therefore must be regulated by other transcriptional regulatory elements. DRAGON shares high sequence homology with two other GPI-anchored membrane proteins: the mouse ortholog of chick repulsive guidance molecule (mRGM), which is expressed in the mouse nervous system in areas complementary to DRAGON, and DRAGON-like muscle (DL-M), the expression of which is restricted to skeletal and cardiac muscle. A comparative genomic analysis indicates that the family of RGM-related genes--mRGM, DRAGON, and DL-M--are highly conserved among mammals, zebrafish, chick, and Caenorhabditis elegans but not Drosophila. DRAGON, RGM, and DL-M mRNA expression in the zebrafish embryo is similar to that in the mouse. Neuronal cell adhesion assays indicate that DRAGON promotes and mRGM reduces adhesion of mouse DRG neurons. We show that DRAGON interacts with itself homophilically. The dynamic expression, ordered spatial localization, and adhesive properties of the RGM-related family of membrane-associated proteins are compatible with specific roles in development.
DRG11是一种在胚胎背根神经节(DRG)和背角神经元中表达的转录因子,在感觉神经回路的发育中发挥作用。我们采用基因组结合策略筛选受DRG11调控的基因的启动子区域。一个其启动子区域与DRG11的DNA结合域结合的基因编码一种新型膜相关[糖基磷脂酰肌醇(GPI)锚定]蛋白,我们将其命名为DRAGON。DRAGON的表达受DRG11的转录调控,并且在胚胎DRG和脊髓中与DRG11共表达。在DRG11基因敲除突变体中,这些区域的DRAGON表达减少。然而,DRAGON在神经管中比DRG11更早表达,并且与DRG11不同,它在大脑中表达,因此必定受其他转录调控元件的调控。DRAGON与另外两种GPI锚定膜蛋白具有高度的序列同源性:鸡排斥导向分子的小鼠直系同源物(mRGM),其在小鼠神经系统中与DRAGON互补的区域表达;以及DRAGON样肌肉蛋白(DL-M),其表达仅限于骨骼肌和心肌。比较基因组分析表明,RGM相关基因家族——mRGM、DRAGON和DL-M——在哺乳动物、斑马鱼、鸡和秀丽隐杆线虫中高度保守,但在果蝇中不保守。斑马鱼胚胎中DRAGON、RGM和DL-M的mRNA表达与小鼠相似。神经元细胞黏附试验表明,DRAGON促进而mRGM降低小鼠DRG神经元的黏附。我们发现DRAGON能同嗜性地与自身相互作用。RGM相关膜相关蛋白家族的动态表达、有序的空间定位和黏附特性与发育中的特定作用相一致。