Evidence map›Paper›PMID 35678925›Full record

ReviewDevelopment genes and evolution2022

Germline specification and axis determination in viviparous and oviparous pea aphids: conserved and divergent features.

Gee-Way Lin, Chen-Yo Chung, Charles E Cook, Ming-Der Lin, Wen-Chih Lee, Chun-Che Chang

Abstract readReview
In one paragraph

Review in Development genes and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Grand challenges in insect systematics.Frontiers in insect science · 2023
    Article
  8. The extended analogy of extraembryonic development in insects and amniotes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  9. Review
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

6 authors.

Gee-Way LinLaboratory for Genomics and Development, College of Bio-Resources and Agriculture, Department of Entomology, National Taiwan University (NTU), No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan.
Chen-Yo ChungLaboratory for Genomics and Development, College of Bio-Resources and Agriculture, Department of Entomology, National Taiwan University (NTU), No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan.
Charles E CookLaboratory for Genomics and Development, College of Bio-Resources and Agriculture, Department of Entomology, National Taiwan University (NTU), No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan.
Ming-Der LinDepartment of Molecular Biology and Human Genetics, Tzu Chi University, Hualien, Taiwan.
Wen-Chih LeeResearch Center for Global SDGs Challenges, Office of Research and Development, Tzu Chi University, Hualien, Taiwan.
Chun-Che ChangLaboratory for Genomics and Development, College of Bio-Resources and Agriculture, Department of Entomology, National Taiwan University (NTU), No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan. chunche@ntu.edu.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aphids are hemimetabolous insects that undergo incomplete metamorphosis without pupation. The annual life cycle of most aphids includes both an asexual (viviparous) and a sexual (oviparous) phase. Sexual reproduction only occurs once per year and is followed by many generations of asexual reproduction, during which aphids propagate exponentially with telescopic development. Here, we discuss the potential links between viviparous embryogenesis and derived developmental features in the pea aphid Acyrthosiphon pisum, particularly focusing on germline specification and axis determination, both of which are key events of early development in insects. We also discuss potential evolutionary paths through which both viviparous and oviparous females might have come to utilize maternal germ plasm to drive germline specification. This developmental strategy, as defined by germline markers, has not been reported in other hemimetabolous insects. In viviparous females, furthermore, we discuss whether molecules that in other insects characterize germ plasm, like Vasa, also participate in posterior determination and how the anterior localization of the hunchback orthologue Ap-hb establishes the anterior-posterior axis. We propose that the linked chain of developing oocytes and embryos within each ovariole and the special morphology of early embryos might have driven the formation of evolutionary novelties in germline specification and axis determination in the viviparous aphids. Moreover, based upon the finding that the endosymbiont Buchnera aphidicola is closely associated with germ cells throughout embryogenesis, we propose presumptive roles for B. aphidicola in aphid development, discussing how it might regulate germline migration in both reproductive modes of pea aphids. In summary, we expect that this review will shed light on viviparous as well as oviparous development in aphids.

Indexed as

AphidsAnimalsFemaleGerm CellsInsect ProteinsOviparityPisum sativumInsect ProteinsBacteriocytesEndosymbiontsGerm plasmHunchbackParthenogenesisVasa

Identifiers

PMID35678925
PMCPMC9329388

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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.