The gene structure and hypervariability of the complete Penaeus monodon Dscam gene

Kantamas Apitanyasai, Shiao Wei Huang, Tze Hann Ng, Shu Ting He, Yu Hsun Huang, Shen Po Chiu, Kuan Chien Tseng, Shih Shun Lin, Wen Chi Chang, James G. Baldwin-Brown, Anthony D. Long, Chu Fang Lo, Hon Tsen Yu, Han Ching Wang

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)


Using two advanced sequencing approaches, Illumina and PacBio, we derive the entire Dscam gene from an M2 assembly of the complete Penaeus monodon genome. The P. monodon Dscam (PmDscam) gene is ~266 kbp, with a total of 44 exons, 5 of which are subject to alternative splicing. PmDscam has a conserved architectural structure consisting of an extracellular region with hypervariable Ig domains, a transmembrane domain, and a cytoplasmic tail. We show that, contrary to a previous report, there are in fact 26, 81 and 26 alternative exons in N-terminal Ig2, N-terminal Ig3 and the entirety of Ig7, respectively. We also identified two alternatively spliced exons in the cytoplasmic tail, with transmembrane domains in exon variants 32.1 and 32.2, and stop codons in exon variants 44.1 and 44.2. This means that alternative splicing is involved in the selection of the stop codon. There are also 7 non-constitutive cytoplasmic tail exons that can either be included or skipped. Alternative splicing and the non-constitutive exons together produce more than 21 million isoform combinations from one PmDscam locus in the P. monodon gene. A public-facing database that allows BLAST searches of all 175 exons in the PmDscam gene has been established at

Original languageEnglish
Article number16595
JournalScientific reports
Issue number1
Publication statusPublished - 2019 Dec 1

All Science Journal Classification (ASJC) codes

  • General


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