Evidence map›Paper›PMID 39633303›Full record

ArticleBMC genomics2024

Mayfly developmental atlas: developmental temporal expression atlas of the mayfly, Ephemera vulgata, reveals short germ-specific hox gene activation.

Wouter P D Makkinje, Sabrina Simon, Inge Breukink, Patrick Verbaarschot, Ryuichiro Machida, M Eric Schranz, Robin van Velzen

Abstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Wouter P D MakkinjeBiosystematics group, Wageningen University & Research, Droevendaalsesteeg 1, Wageningen, The Netherlands, 6708PB. wouter.makkinje@wur.nl.ORCID https://orcid.org/0000-0002-8340-8591
Sabrina SimonBiosystematics group, Wageningen University & Research, Droevendaalsesteeg 1, Wageningen, The Netherlands, 6708PB.ORCID https://orcid.org/0000-0001-8560-0985
Inge BreukinkBiosystematics group, Wageningen University & Research, Droevendaalsesteeg 1, Wageningen, The Netherlands, 6708PB.ORCID https://orcid.org/0009-0004-6864-5814
Patrick VerbaarschotBiosystematics group, Wageningen University & Research, Droevendaalsesteeg 1, Wageningen, The Netherlands, 6708PB.ORCID https://orcid.org/0009-0004-7365-6411
Ryuichiro MachidaSugadaira Research Station, Mountain Science Center, University of Tsukuba, Sugadaira Kogen, Ueda, Nagano, 386-2204, Japan.
M Eric SchranzBiosystematics group, Wageningen University & Research, Droevendaalsesteeg 1, Wageningen, The Netherlands, 6708PB.ORCID https://orcid.org/0000-0001-6777-6565
Robin van VelzenBiosystematics group, Wageningen University & Research, Droevendaalsesteeg 1, Wageningen, The Netherlands, 6708PB. robin.vanvelzen@wur.nl.ORCID https://orcid.org/0000-0002-6444-7608

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver the course of evolution, insects have seen drastic changes in their mode of development. While insects with derived modes of development have been studied extensively, information on ancestral modes of development is lacking. To address this, we selected a member of one of the earliest lineages of extant flying insects, serving as an outgroup to the modern winged insects, the short germ, non-model mayfly Ephemera vulgata Linnaeus (Insecta: Ephemeroptera, Ephemeridae). We document the embryonic morphology throughout its development and establish a global temporal expression atlas.

resultsDAPI staining was used to visualise developmental morphology to provide a frame of reference for the sequenced timepoints. A transcriptome was assembled from 3.2 billion Illumina RNAseq reads divided in 12 timepoints with 3 replicates per timepoint consisting of 35,091 putative genes. We identified 6,091 significantly differentially expressed genes (DEGs) and analysed them for broad expression patterns via gene ontology (GO) as well as for specific genes of interest. This revealed a U-shaped relationship between the sum of DEGs and developmental timepoints, over time, with the lowest number of DEGs at 72 hours after egg laying (hAEL). Based on a principal component analysis of sequenced timepoints, overall development could be divided into four stages, with a transcriptional turning point around katatrepsis. Expression patterns of zld and smg showed a persistent negative correlation and revealed the maternal-to-zygotic transition (MZT), occurring 24 hAEL. The onset of development of some major anatomical structures, including the head, body, respiratory system, limb, muscle, and eye, are reported. Finally, we show that the ancestral short germ sequential mode of segmentation translates to a sequential Hox gene activation and find diverging expression patterns for lab and pb. We incorporate these patterns and morphological observations to an overview of the developmental timeline.

conclusionsWith our comprehensive differential expression study, we demonstrate the versatility of our global temporal expression atlas. It has the capacity to contribute significantly to phylogenetic insights in early-diverging insect developmental biology and can be deployed in both molecular and genomic applications for future research.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsEphemeropteraGene Expression ProfilingGenes, HomeoboxTranscriptional ActivationTranscriptomeEmbryogenesisEvo-devoHox genesMayflyMorphologyTranscriptomics

Identifiers

PMID39633303
PMCPMC11616370

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Registered trials

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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.