Penaeus monodon Dscam (PmDscam) has a highly diverse cytoplasmic tail and is the first membrane-bound shrimp Dscam to

Pin-Hsiang Chou1, Hao-Shuo Chang, I-Tung Chen

  • 1Institute of Biotechnology, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan 701, Taiwan.

Fish & Shellfish Immunology
|February 23, 2011
PubMed

Insights

Shrimp Down syndrome cell adhesion molecule (Dscam) exhibits both membrane-bound and tail-less forms, crucial for invertebrate adaptive immunity. Alternative splicing generates extensive extracellular and cytoplasmic tail variants, expanding immune recognition capabilities.

Area of Science:

  • Immunology
  • Molecular Biology
  • Genetics

Background:

  • Down syndrome cell adhesion molecule (Dscam) is implicated in invertebrate adaptive immunity.
  • Dscam features a signaling cytoplasmic tail and a variable extracellular region for pathogen recognition.
  • Previous work identified a tail-less Dscam in Litopenaeus vannamei.

Purpose of the Study:

  • To identify and characterize membrane-bound forms of shrimp Dscam.
  • To investigate the molecular mechanisms underlying Dscam diversity in Penaeus monodon.
  • To analyze the phylogenetic relationships of crustacean Dscam.

Main Methods:

  • Isolation of Penaeus monodon Dscam (PmDscam).
  • Phylogenetic analysis of crustacean Dscam sequences.
  • Analysis of alternative splicing events in PmDscam variants.
  • Genomic organization analysis and modeling of Dscam expression.

Main Results:

  • The first membrane-bound form of shrimp Dscam (PmDscam) was isolated, existing alongside tail-less forms.
  • Phylogenetic analysis revealed distinct clades for shrimp and water flea Dscams, separate from insect Dscams.
  • Extracellular and transmembrane variants arise from mutually exclusive alternative splicing.
  • Cytoplasmic tail variants are generated by exon inclusion/exclusion.

Conclusions:

  • PmDscam contributes to the diversity of immune molecules in shrimp.
  • Alternative splicing of PmDscam generates significant molecular variation for immune responses.
  • A model is proposed for generating both tail-less and membrane-bound PmDscam forms via Type III polyadenylation.