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Structural basis for the self-recognition of sDSCAM in Chelicerata.

Jie ChengYamei YuXingyu WangXi ZhengTing LiuDaojun HuYongfeng JinYing LaiTian-Min FuQiang Chen
Published in: Nature communications (2023)
To create a functional neural circuit, neurons develop a molecular identity to discriminate self from non-self. The invertebrate Dscam family and vertebrate Pcdh family are implicated in determining synaptic specificity. Recently identified in Chelicerata, a shortened Dscam (sDscam) has been shown to resemble the isoform-generating characters of both Dscam and Pcdh and represent an evolutionary transition. Here we presented the molecular details of sDscam self-recognition via both trans and cis interactions using X-ray crystallographic data and functional assays. Based on our results, we proposed a molecular zipper model for the assemblies of sDscam to mediate cell-cell recognition. In this model, sDscam utilized FNIII domain to form side-by-side interactions with neighboring molecules in the same cell while established hand-in-hand interactions via Ig1 domain with molecules from another cell around. Together, our study provided a framework for understanding the assembly, recognition, and evolution of sDscam.
Keyphrases
  • single cell
  • cell therapy
  • structural basis
  • spinal cord
  • high throughput
  • gene expression
  • computed tomography
  • spinal cord injury
  • single molecule
  • data analysis