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A chelicerate-specific burst of nonclassical Dscam diversity

Authors :
Guozheng Cao
Yang Shi
Jian Zhang
Hongru Ma
Shouqing Hou
Haiyang Dong
Weiling Hong
Shuo Chen
Hao Li
Yandan Wu
Pengjuan Guo
Xu Shao
Bingbing Xu
Feng Shi
Yijun Meng
Yongfeng Jin
Source :
BMC Genomics, Vol 19, Iss 1, Pp 1-14 (2018)
Publication Year :
2018
Publisher :
BMC, 2018.

Abstract

Abstract Background The immunoglobulin (Ig) superfamily receptor Down syndrome cell adhesion molecule (Dscam) gene can generate tens of thousands of isoforms via alternative splicing, which is essential for both nervous and immune systems in insects. However, further information is required to develop a comprehensive view of Dscam diversification across the broad spectrum of Chelicerata clades, a basal branch of arthropods and the second largest group of terrestrial animals. Results In this study, a genome-wide comprehensive analysis of Dscam genes across Chelicerata species revealed a burst of nonclassical Dscams, categorised into four types—mDscam, sDscamα, sDscamβ, and sDscamγ—based on their size and structure. Although the mDscam gene class includes the highest number of Dscam genes, the sDscam genes utilise alternative promoters to expand protein diversity. Furthermore, we indicated that the 5′ cassette duplicate is inversely correlated with the sDscam gene duplicate. We showed differential and sDscam- biased expression of nonclassical Dscam isoforms. Thus, the Dscam isoform repertoire across Chelicerata is entirely dominated by the number and expression levels of nonclassical Dscams. Taken together, these data show that Chelicerata evolved a large conserved and lineage-specific repertoire of nonclassical Dscams. Conclusions This study showed that arthropods have a large diversified Chelicerata-specific repertoire of nonclassical Dscam isoforms, which are structurally and mechanistically distinct from those of insects. These findings provide a global framework for the evolution of Dscam diversity in arthropods and offer mechanistic insights into the diversification of the clade-specific Ig superfamily repertoire.

Details

Language :
English
ISSN :
14712164
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Genomics
Publication Type :
Academic Journal
Accession number :
edsdoj.9fcf2aa33ee14bd0b86fe57039b8cb6c
Document Type :
article
Full Text :
https://doi.org/10.1186/s12864-017-4420-0