Evidence map›Paper›PMID 30249207›Full record

ArticleBMC genomics2018

Analysis of Drosophila melanogaster testis transcriptome.

Viktor Vedelek, László Bodai, Gábor Grézal, Bence Kovács, Imre M Boros, Barbara Laurinyecz, Rita Sinka

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 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

  1. Review
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  4. Metabolic Regulation in the Maintenance ofInternational journal of molecular sciences · 2026
    Review
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  16. microPublication biology · 2025
    Article
  17. An orphan gene is essential for efficient sperm entry into eggs inbioRxiv : the preprint server for biology · 2024
    Article
  18. Article
  19. Article
  20. 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

7 authors.

Viktor VedelekDepartment of Genetics, University of Szeged, Szeged, Hungary.
László BodaiDepartment of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.
Gábor GrézalDepartment of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.
Bence KovácsDepartment of Genetics, University of Szeged, Szeged, Hungary.
Imre M BorosDepartment of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.
Barbara LaurinyeczDepartment of Genetics, University of Szeged, Szeged, Hungary.
Rita SinkaDepartment of Genetics, University of Szeged, Szeged, Hungary. rsinka@bio.u-szeged.hu.ORCID http://orcid.org/0000-0003-4040-4184

Funding

NKFIH GINOP-2.3.2-15-2016-00032NKFIH GINOP-2.3.2-15-2016-00035NKFIH K112294NKFIH NF101001
6 · The paper itself

Abstract

backgroundThe formation of matured and individual sperm involves a series of molecular and spectacular morphological changes of the developing cysts in Drosophila melanogaster testis. Recent advances in RNA Sequencing (RNA-Seq) technology help us to understand the complexity of eukaryotic transcriptomes by dissecting different tissues and developmental stages of organisms. To gain a better understanding of cellular differentiation of spermatogenesis, we applied RNA-Seq to analyse the testis-specific transcriptome, including coding and non-coding genes.

resultsWe isolated three different parts of the wild-type testis by dissecting and cutting the different regions: 1.) the apical region, which contains stem cells and developing spermatocytes 2.) the middle region, with enrichment of meiotic cysts 3.) the basal region, which contains elongated post-meiotic cysts with spermatids. Total RNA was isolated from each region and analysed by next-generation sequencing. We collected data from the annotated 17412 Drosophila genes and identified 5381 genes with significant transcript accumulation differences between the regions, representing the main stages of spermatogenesis. We demonstrated for the first time the presence and region specific distribution of 2061 lncRNAs in testis, with 203 significant differences. Using the available modENCODE RNA-Seq data, we determined the tissue specificity indices of Drosophila genes. Combining the indices with our results, we identified genes with region-specific enrichment in testis.

conclusionBy multiple analyses of our results and integrating existing knowledge about Drosophila melanogaster spermatogenesis to our dataset, we were able to describe transcript composition of different regions of Drosophila testis, including several stage-specific transcripts. We present searchable visualizations that can facilitate the identification of new components that play role in the organisation and composition of different stages of spermatogenesis, including the less known, but complex regulation of post-meiotic stages.

Indexed as

TranscriptomeAnimalsCytoskeletal ProteinsDrosophila melanogasterDrosophila ProteinsGene Expression ProfilingGene OntologyHeat-Shock ProteinsMaleMetabolic Networks and PathwaysProteasome Endopeptidase ComplexRNA, Long NoncodingSequence Analysis, RNATestisUbiquitinCytoskeletal ProteinsDrosophila ProteinsHeat-Shock ProteinsProteasome Endopeptidase ComplexRNA, Long NoncodingUbiquitinDrosophilaRNA sequencingSpermatogenesisTestisTranscriptome

Identifiers

PMID30249207
PMCPMC6154878

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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.