Yimlamai Dean, Konnikova Liza, Moss Larry G, Jay Daniel G
Cellular and Molecular Physiology, Tufts University School of Medicine, 136 Harrison Avenue, M and V 709, Boston, MA 02111, USA.
Dev Biol. 2005 Mar 1;279(1):44-57. doi: 10.1016/j.ydbio.2004.12.001.
The Down syndrome cell adhesion molecule (Dscam) is a protein overexpressed in the brains of Down syndrome patients and implicated in mental retardation. Dscam is involved in axon guidance and branching in Drosophila, but cellular roles in vertebrates have yet to be elucidated. To understand its role in vertebrate development, we cloned the zebrafish homolog of Dscam and showed that it shares high amino acid identity and structure with the mammalian homologs. Zebrafish dscam is highly expressed in developing neurons, similar to what has been described in Drosophila and mouse. When dscam expression is diminished by morpholino injection, embryos display few neurons and their axons do not enter stereotyped pathways. Zebrafish dscam is also present at early embryonic stages including blastulation and gastrulation. Its loss results in early morphogenetic defects. dscam knockdown results in impaired cell movement during epiboly as well as in subsequent stages. We propose that migrating cells utilize dscam to remodel the developing embryo.
唐氏综合征细胞粘附分子(Dscam)是一种在唐氏综合征患者大脑中过度表达的蛋白质,与智力发育迟缓有关。Dscam在果蝇中参与轴突导向和分支,但在脊椎动物中的细胞作用尚未阐明。为了解其在脊椎动物发育中的作用,我们克隆了斑马鱼的Dscam同源物,并表明它与哺乳动物同源物具有高度的氨基酸同一性和结构。斑马鱼dscam在发育中的神经元中高度表达,类似于在果蝇和小鼠中所描述的情况。当通过吗啉代注射减少dscam表达时,胚胎显示出很少的神经元,并且它们的轴突不会进入定型途径。斑马鱼dscam在包括囊胚形成和原肠胚形成在内的早期胚胎阶段也存在。它的缺失会导致早期形态发生缺陷。dscam敲低导致外包期以及随后阶段的细胞运动受损。我们提出迁移细胞利用dscam重塑发育中的胚胎。