Evidence map›Paper›PMID 32353187›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2020

Tissue-specific expression of ribosomal protein paralogue eRpL22-like in Drosophila melanogaster eye development.

Brett W Gershman, Caroline E Pritchard, Kenneth P Chaney, Vassie C Ware

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 41% of its field
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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Ribosomal protein paralogues in ribosome specialization.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  3. Ribosome Structural Changes Dynamically Affect Ribosome Function.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Regulation of ribosomal protein genes: An ordered anarchy.Wiley interdisciplinary reviews. RNA · 2021
    Review
  7. Homeostatic Roles of the Proteostasis Network in Dendrites.Frontiers in cellular neuroscience · 2020
    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

4 authors at 2 institutions in 1 country.

Brett W GershmanDepartment of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania, USA.ORCID 0000-0002-2130-6792
Caroline E PritchardDepartment of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania, USA.ORCID 0000-0001-8587-680X
Kenneth P ChaneyDepartment of Computer and Information Science, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0003-1768-6136
Vassie C WareDepartment of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania, USA.ORCID 0000-0003-1604-5628
Lehigh University · USUniversity of Pennsylvania · US

Funding

Exploring Mechanisms of Specialized Ribosome Function in the Male Germline in Drosophila MelanogasterR15GM132889 · NIGMS · LEHIGH UNIVERSITY · PI WARE, VASSIE C. · 2019 to 2019
$457k
Lehigh UniversityNIGMS NIH HHS R15 GM132889NIH HHS 1R15GM132889-01
6 · The paper itself

Abstract

backgroundDifferences in core or tissue-specific ribosomal protein (Rp) composition within ribosomes contribute to ribosome heterogeneity and functional variability. Yet, the degree to which ribosome heterogeneity modulates development is unknown. The Drosophila melanogaster eRpL22 family contains structurally diverse paralogues, eRpL22 and eRpL22-like. Unlike ubiquitously expressed eRpL22, eRpL22-like expression is tissue-specific, notably within the male germline and the eye. We investigated expression within the developing eye to uncover tissue/cell types where specific paralogue roles might be defined.

resultsImmunohistochemistry analysis confirms ubiquitous eRpL22 expression throughout eye development. In larvae, eRpL22-like is ubiquitously expressed, but highly enriched in the peripodial epithelium (PE). In early pupae, eRpL22-like is broadly distributed in multiple cell types, but later, is primarily enriched in interommatidial hair cells (IoHC). Adult patterns include the ring of accessory cells around ommatidia. Adult retinae IoHC patterning phenotypes (shown by scanning electron microscopy) may be linked to RNAi-mediated eRpL22-like depletion within larval PE. Immunoblots and polysome profile analyses show multiple variants of eRpL22-like across development, with the variant at the expected molecular mass co-sedimenting with active ribosomes.

conclusionOur data reveal differential patterns of eRpL22-like expression relative to eRpL22 and suggest a specific role for eRpL22-like in developmental patterning of the eye.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianEyeOrgan SpecificityRibosomal ProteinsDrosophila ProteinsRibosomal Proteinsdevelopmentgene expressioninterommatidial hair cellperipodial epitheliumribosomal proteins

Identifiers

PMID32353187
PMCPMC8109839
OpenAlexW3022022461

What OpenQuestion holds

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Registered trials

None linked

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.