Evidence map›Paper›PMID 17611220›Full record

ArticleDevelopment (Cambridge, England)2007

Translational control of meiotic cell cycle progression and spermatid differentiation in male germ cells by a novel eIF4G homolog.

Catherine C Baker, Margaret T Fuller

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

46 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Dichotomous transcriptome divergence at the cell-type level between thebioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
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  13. Review
  14. Unconventional translation initiation factor EIF2A is required for Drosophila spermatogenesis.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
  15. Article
  16. Single-cyst transcriptome analysis ofDevelopment (Cambridge, England) · 2020
    Article
  17. Review
  18. Development (Cambridge, England) · 2019
    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

2 authors at 1 institution in 1 country.

Catherine C BakerDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305-5329, USA.
Margaret T Fuller
Stanford University · US

Funding

ROLE OF PHOSPHODIESTERASES IN GAMETOGENESISU54HD031398 · NICHD · STANFORD UNIVERSITY · PI REIJO-PERA, RENEE · 1997 to 2007
$11.1M
TRAINING IN NEONATAL BIOLOGYT32HD007249 · NICHD · STANFORD UNIVERSITY · PI STEVENSON, DAVID K · 1985 to 2013
$4.4M
Stanford University Center for Reproductive and Stem Cell biologyP50HD068158 · NICHD · STANFORD UNIVERSITY · PI REIJO PERA, RENEE A · 2014 to 2015
$3.3M
Control of meiotic cell cycle progression in malesF32GM071260 · NIGMS · STANFORD UNIVERSITY · PI BAKER, CATHERINE CRAIG · 2005 to 2006
$93k
NICHD NIH HHS P50 HD068158NICHD NIH HHS T32 HD007249NICHD NIH HHS U54 HD031398NICHD NIH HHS U54-HD31398NIGMS NIH HHS 1 F32 GM071260NIGMS NIH HHS F32 GM071260
6 · The paper itself

Abstract

Translational control is crucial for proper timing of developmental events that take place in the absence of transcription, as in meiotic activation in oocytes, early embryogenesis in many organisms, and spermatogenesis. Here we show that a novel form of the translation initiation complex component eIF4G in Drosophila, eIF4G2, is required specifically for male germ cells to undergo meiotic division and proper spermatid differentiation. Flies mutant for eIF4G2 are viable and female fertile but male sterile. Spermatocytes form, but the germ cells in mutant males skip the major events of the meiotic divisions and form aberrant spermatids with large nuclei. Consistent with the failure to undergo the meiotic divisions, function of eIF4G2 is required post-transcriptionally for normal accumulation of the core cell cycle regulatory proteins Twine and CycB in mature spermatocytes. Loss of eIF4G2 function also causes widespread defects in spermatid differentiation. Although differentiation markers Dj and Fzo are expressed in late-stage eIF4G2 mutant germ cells, several key steps of spermatid differentiation fail, including formation of a compact mitochondrial derivative and full elongation. Our results suggest that an alternate form of the translation initiation machinery may be required for regulation and execution of key steps in male germ cell differentiation.

Indexed as

Cell DifferentiationGene Expression Regulation, DevelopmentalProtein BiosynthesisAnimalsAnimals, Genetically ModifiedCell CycleCells, CulturedDrosophilaDrosophila ProteinsEukaryotic Initiation Factor-4GFertilityMaleMeiosisSequence Homology, Amino AcidSpermatidsSpermatozoaDrosophila ProteinseIF4G2 protein, DrosophilaEukaryotic Initiation Factor-4G

Identifiers

PMID17611220
PMCPMC4620998
OpenAlexW1994686571

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.