Evidence map›Paper›PMID 29351731›Full record

ArticleBMC genomics2018

A chelicerate-specific burst of nonclassical Dscam diversity.

Guozheng Cao, Yang Shi, Jian Zhang, Hongru Ma, Shouqing Hou, Haiyang Dong, Weiling Hong, Shuo Chen, Hao Li, Yandan Wu and 6 more

Abstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Structure and evolution of neuronal wiring receptors and ligands.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
  5. Article
  6. Chelicerata sDscam isoforms combine homophilic specificities to define unique cell recognition.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Revisiting Dscam diversity: lessons from clustered protocadherins.Cellular and molecular life sciences : CMLS · 2019
    Review
  8. Frontiers in physiology · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Guozheng CaoZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Yang ShiZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Jian ZhangZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Hongru MaZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Shouqing HouZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Haiyang DongZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Weiling HongZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Shuo ChenZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Hao LiZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Yandan WuZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Pengjuan GuoZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Xu ShaoZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Bingbing XuZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Feng ShiZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China.
Yijun MengCollege of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, Zhejiang, ZJ310018, People's Republic of China.
Yongfeng JinZhejiang University, Institute of Biochemistry, College of Life Sciences, Hangzhou, Zhejiang, ZJ310058, People's Republic of China. jinyf@zju.edu.cn.

Funding

the National Natural Science Foundation of China 31630089, 31430050, 91740104
6 · The paper itself

Abstract

backgroundThe 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.

resultsIn 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.

conclusionsThis 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.

Indexed as

AnimalsArthropod ProteinsArthropodsCell Adhesion MoleculesGene ExpressionGenes, DuplicateGenetic VariationGenomePhylogenyProtein IsoformsArthropod ProteinsCell Adhesion MoleculesProtein IsoformsAlternative promoterAlternative splicingChelicerateDscamExon duplicationGene duplication

Identifiers

PMID29351731
PMCPMC5775551

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.