Evidence map›Paper›PMID 8194530›Full record

ArticleThe EMBO journal1994

Suppression of DNA replication via Mos function during meiotic divisions in Xenopus oocytes.

N Furuno, M Nishizawa, K Okazaki, H Tanaka, J Iwashita, N Nakajo, Y Ogawa, N Sagata

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

67 citing papers in PubMed, 233 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Dissection of the Ovulatory Process UsingFrontiers in cell and developmental biology · 2020
    Review
  8. MPF-based meiotic cell cycle control: Half a century of lessons from starfish oocytes.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2018
    Review
  9. Review
  10. Article
  11. Meiosis: an overview of key differences from mitosis.Cold Spring Harbor perspectives in biology · 2015
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. How to halve ploidy: lessons from budding yeast meiosis.Cellular and molecular life sciences : CMLS · 2012
    Review
  19. Article
  20. Article

7 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

N FurunoDivision of Molecular Genetics, Kurume University, Fukuoka, Japan.
M Nishizawa
K Okazaki
H Tanaka
J Iwashita
N Nakajo
Y Ogawa
N Sagata
Kurume University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meiosis is characterized by the absence of DNA replication between the two successive divisions. In Xenopus eggs, the ability to replicate DNA develops during meiotic maturation, but is normally suppressed until fertilization. Here we show that development of the DNA-replicating ability depends on new protein synthesis during meiosis I, and that mere ablation of the endogenous c-mos product Mos allows maturing oocytes to enter interphase and replicate DNA just after meiosis I. Moreover, we demonstrate that during normal maturation cdc2 kinase undergoes precocious inactivation in meiosis I and then premature reactivation before meiosis II; importantly, this premature cdc2 reactivation absolutely requires Mos function and its direct inhibition by a dominant-negative cdc2 mutant also results in nuclear reformation and DNA replication immediately after meiosis I. These findings indicate that suppression of DNA replication during meiotic divisions in Xenopus oocytes is accomplished by the Mos-mediated premature reactivation of cdc2 kinase. We suggest that these mechanisms for suppressing DNA replication may be specific for meiosis in animal oocytes, and that the ultimate biological function, including the well known cytostatic factor activity, of Mos during meiotic maturation may be to prevent undesirable DNA replication or parthenogenetic activation before fertilization.

Indexed as

DNA ReplicationAnimalsCDC2 Protein KinaseCycloheximideFemaleMaturation-Promoting FactorMeiosisModels, GeneticOligonucleotides, AntisenseOocytesParthenogenesisProto-Oncogene Proteins c-mosXenopusCDC2 Protein KinaseCycloheximideMaturation-Promoting FactorOligonucleotides, AntisenseProto-Oncogene Proteins c-mos

Identifiers

PMID8194530
PMCPMC395105
OpenAlexW174741394

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.