Evidence map›Paper›PMID 24297695›Full record

ArticleParasitology research2014

Transcriptome profilings of female Schistosoma japonicum reveal significant differential expression of genes after pairing.

Jun Sun, Su-Wen Wang, Chen Li, Wei Hu, Yi-Jiu Ren, Jin-Qiang Wang

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Article in Parasitology research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

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14citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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14 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jun SunInstitute for Infectious Diseases and Vaccine Development, Tongji University School of Medicine, Shanghai, 200092, People's Republic of China, swksj@tongji.edu.cn.
Su-Wen Wang
Chen Li
Wei Hu
Yi-Jiu Ren
Jin-Qiang Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pairing of Schistosoma japonicum initiates female development, leads to female sexual maturation, and maintains this mature state. To understand the mechanism involved in these processes, we studied parasites isolated from single- and double-sex cercariae-infected mice using deep-sequencing analysis, Solexa, to uncover pair-regulated transcriptional profiles. In this study, we report the results of high-throughput tag-sequencing (Tag-seq) analysis of the transcriptome of female worms 18 and 23 days postsingle- and double-sex infections. We sequenced over 3 million tags, obtained a total of 14,034, 27,251, 22,755, and 22,555 distinct tags corresponding to 5,773, 9,794, 8,885, and 8,870 tag-mapped genes for 23-day-old female schistosomula from double-sex infections (23DSI), 23-day-old female schistosomula from single-sex infections (23SSI), 18-day-old female schistosomula from double-sex infections (18DSI), and 18-day-old female schistosomula from single-sex infections (18SSI), respectively. Analyses of differentially expressed genes revealed similarities in the gene expression profiles between 18SSI and 18DSI as well as rational differential gene expression between 18SSI and 23SSI. However, fewer upregulated genes were found in 23DSI compared with 18DSI. Of the 3,446 differentially expressed genes between 23DSI and 23SSI, 2,913 genes were upregulated in 23SSI, whereas only 533 genes were upregulated in 23DSI. In these upregulated genes in 23DSI, phosphoglycerate mutase, superoxide dismutase, egg antigen, ribosomal proteins, ferritin-1 heavy chain, and eukaryotic translation initiation factor 2 were detected. Detection of these genes suggests that gene expression in 23DSI is specialized for functions such as promotion and maintenance of female sexual maturation and egg production. Quantitative real-time (RT)-PCR analysis confirmed the Solexa results, thereby supporting the reliability of the system. Our results offer new insights into the biological significance of pairing, which directs the expression of genes specific for sexual maturation and egg production.

Indexed as

TranscriptomeAnimalsFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalGene LibraryHigh-Throughput Nucleotide SequencingMiceSchistosoma japonicumSexual Maturation

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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.