Evidence map›Paper›PMID 34388374›Full record

ArticleCurrent biology : CB2021

The DNA-to-cytoplasm ratio broadly activates zygotic gene expression in Xenopus.

David Jukam, Rishabh R Kapoor, Aaron F Straight, Jan M Skotheim

Open access · greenAbstract read
In one paragraph

Article in Current biology : CB, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-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

22 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Regulation of zygotic genome activation by the nucleocytoplasmic ratio.Frontiers in cell and developmental biology · 2026
    Review
  3. Reconstitution of genome remodeling usingFrontiers in cell and developmental biology · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Quantifying Nascent Transcription in Early Embryogenesis.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  9. Article
  10. Review
  11. Review
  12. Collective effects of cell cleavage dynamics.Frontiers in cell and developmental biology · 2024
    Review
  13. Manipulation of Embryonic Cleavage Geometry Using Magnetic Tweezers.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  14. Principles of genome activation in the early embryo.Current opinion in genetics & development · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

4 authors at 1 institution in 1 country.

David JukamDepartment of Biology, Stanford University, Stanford, CA 94305, USA; Department of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USA.
Rishabh R KapoorDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Aaron F StraightDepartment of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: astraigh@stanford.edu.
Jan M SkotheimDepartment of Biology, Stanford University, Stanford, CA 94305, USA. Electronic address: skotheim@stanford.edu.
Stanford University · US

Funding

Control and coordination of the maternal-to-zygotic transitionR01HD085135 · NICHD · STANFORD UNIVERSITY · PI SKOTHEIM, JAN M, STRAIGHT, AARON F · 2016 to 2020
$1.6M
Determining the dynamic mechanisms regulating the maternal-to-zygotic transitionF32GM108295 · NIGMS · STANFORD UNIVERSITY · PI JUKAM, DAVID M · 2013 to 2016
$161k
NICHD NIH HHS R01 HD085135NIGMS NIH HHS F32 GM108295
6 · The paper itself

Abstract

In multicellular animals, the first major event after fertilization is the switch from maternal to zygotic control of development. During this transition, zygotic gene transcription is broadly activated in an otherwise quiescent genome in a process known as zygotic genome activation (ZGA). In fast-developing embryos, ZGA often overlaps with the slowing of initially synchronous cell divisions at the mid-blastula transition (MBT). Initial studies of the MBT led to the nuclear-to-cytoplasmic ratio model where MBT timing is regulated by the exponentially increasing amounts of some nuclear component "N" titrated against a fixed cytoplasmic component "C." However, more recent experiments have been interpreted to suggest that ZGA is independent of the N/C ratio. To determine the role of the N/C ratio in ZGA, we generated Xenopus frog embryos with ∼3-fold differences in genomic DNA (i.e., N) by using X. tropicalis sperm to fertilize X. laevis eggs with or without their maternal genome. Resulting embryos have otherwise identical X. tropicalis genome template amounts, embryo sizes, and X. laevis maternal environments. We generated transcriptomic time series across the MBT in both conditions and used X. tropicalis paternally derived mRNA to identify a high-confidence set of exclusively zygotic transcripts. Both ZGA and the increase in cell-cycle duration are delayed in embryos with ∼3-fold less DNA per cell. Thus, DNA is an important component of the N/C ratio, which is a critical regulator of zygotic genome activation in Xenopus embryos.

Indexed as

BlastulaZygoteAnimalsCytoplasmDNAGene ExpressionGene Expression Regulation, DevelopmentalXenopus laevisDNAcell sizeearly Xenopus developmentembryogenesismaternal-to-zygotic transitionMBTmid-blastula transitionMZTN/C ratiotranscriptionzygotic genome activation

Identifiers

PMID34388374
PMCPMC8511243
OpenAlexW3187699856

What Socratic holds

Textmetadata
LicenceTDM
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.