Evidence map›Paper›PMID 37872135›Full record

ArticleNature communications2023

Metabolic regulation of proteome stability via N-terminal acetylation controls male germline stem cell differentiation and reproduction.

Charlotte M François, Thomas Pihl, Marion Dunoyer de Segonzac, Chloé Hérault, Bruno Hudry

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cells · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Mitochondrial Differentiation during Spermatogenesis: Lessons fromInternational journal of molecular sciences · 2024
    Review
  14. 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

5 authors at 1 institution in 1 country.

Charlotte M FrançoisUniversité Côte d'Azur, CNRS, Inserm, Institut de Biologie Valrose, Nice, 06108, France.ORCID http://orcid.org/0009-0003-0090-3170
Thomas PihlUniversité Côte d'Azur, CNRS, Inserm, Institut de Biologie Valrose, Nice, 06108, France.ORCID http://orcid.org/0000-0002-3617-2088
Marion Dunoyer de SegonzacUniversité Côte d'Azur, CNRS, Inserm, Institut de Biologie Valrose, Nice, 06108, France.
Chloé HéraultUniversité Côte d'Azur, CNRS, Inserm, Institut de Biologie Valrose, Nice, 06108, France.ORCID http://orcid.org/0009-0000-7581-0698
Bruno HudryUniversité Côte d'Azur, CNRS, Inserm, Institut de Biologie Valrose, Nice, 06108, France. Bruno.HUDRY@univ-cotedazur.fr.ORCID http://orcid.org/0000-0003-1299-843X
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular mechanisms connecting cellular metabolism with differentiation remain poorly understood. Here, we find that metabolic signals contribute to stem cell differentiation and germline homeostasis during Drosophila melanogaster spermatogenesis. We discovered that external citrate, originating outside the gonad, fuels the production of Acetyl-coenzyme A by germline ATP-citrate lyase (dACLY). We show that this pathway is essential during the final spermatogenic stages, where a high Acetyl-coenzyme A level promotes NatB-dependent N-terminal protein acetylation. Using genetic and biochemical experiments, we establish that N-terminal acetylation shields key target proteins, essential for spermatid differentiation, from proteasomal degradation by the ubiquitin ligase dUBR1. Our work uncovers crosstalk between metabolism and proteome stability that is mediated via protein post-translational modification. We propose that this system coordinates the metabolic state of the organism with gamete production. More broadly, modulation of proteome turnover by circulating metabolites may be a conserved regulatory mechanism to control cell functions.

Indexed as

Drosophila melanogasterProteomeAcetylationAcetyl Coenzyme AAnimalsCell DifferentiationMaleProtein Processing, Post-TranslationalReproductionAcetyl Coenzyme AProteome

Identifiers

PMID37872135
PMCPMC10593830
OpenAlexW4387871262

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.