Evidence map›Paper›PMID 30880011›Full record

ArticleCurrent biology : CB2019

A Link between Deoxyribonucleotide Metabolites and Embryonic Cell-Cycle Control.

Boyang Liu, Franziska Winkler, Marco Herde, Claus-Peter Witte, Jörg Großhans

Open access · bronzeAbstract read
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In one paragraph

Article in Current biology : CB, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Collective effects of cell cleavage dynamics.Frontiers in cell and developmental biology · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Cell cycle control during early embryogenesis.Development (Cambridge, England) · 2021
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Boyang LiuInstitute for Developmental Biochemistry, Medical School, Georg August University Göttingen, Justus-von-Liebig-Weg 11, 37077 Göttingen, Germany.
Franziska WinklerInstitute for Developmental Biochemistry, Medical School, Georg August University Göttingen, Justus-von-Liebig-Weg 11, 37077 Göttingen, Germany.
Marco HerdeInstitute of Plant Nutrition, Leibniz University Hannover, Herrenhäuser Str. 2, 30419 Hannover, Germany.
Claus-Peter WitteInstitute of Plant Nutrition, Leibniz University Hannover, Herrenhäuser Str. 2, 30419 Hannover, Germany.
Jörg GroßhansInstitute for Developmental Biochemistry, Medical School, Georg August University Göttingen, Justus-von-Liebig-Weg 11, 37077 Göttingen, Germany. Electronic address: jgrossh@gwdg.de.
University of Göttingen · DELeibniz University Hannover · DE

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
NIH HHS P40 OD018537
6 · The paper itself

Abstract

The egg contains maternal RNAs and proteins, which have instrumental functions in patterning and morphogenesis. Besides these, the egg also contains metabolites, whose developmental functions have been little investigated. For example, the rapid increase of DNA content during the fast embryonic cell cycles poses high demands on the supply of deoxyribonucleotides (dNTPs), which may be synthesized in the embryo or maternally provided [1, 2]. Here, we analyze the role of dNTP in early Drosophila embryos. We found that dNTP levels initially decreased about 2-fold before reaching stable levels at the transition from syncytial to cellular blastoderm. Employing a mutant of the metabolic enzyme serine hydroxymethyl transferase (SHMT), which is impaired in the embryonic synthesis of deoxythymidine triphosphate (dTTP), we found that the maternal supply of dTTP was specifically depleted by interphase 13. SHMT mutants showed persistent S phase, replication stress, and a checkpoint-dependent cell-cycle arrest in NC13, depending on the loss of dTTP. The cell-cycle arrest in SHMT mutants was suppressed by reduced zygotic transcription. Consistent with the requirement of dTTP for cell-cycle progression, increased dNTP levels accelerated the cell cycle in embryos lacking zygotic transcription. We propose a model that both a limiting dNTP supply and interference of zygotic transcription with DNA replication [3] elicit DNA replication stress and checkpoint activation. Our study reveals a specific mechanism of how dNTP metabolites contribute to the embryonic cell-cycle control.

Indexed as

Cell Cycle CheckpointsAnimalsDeoxyribonucleotidesDrosophilaEmbryo, NonmammalianDeoxyribonucleotidesblastodermcell cycledeoxyribonucleotide metabolismDNA checkpointDrosophilahaploidreplication stressRNRSHMTzygotic transcription

Identifiers

PMID30880011
OpenAlexW2921171445

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.