Evidence map›Paper›PMID 19073997›Full record

ArticleBiology of reproduction2009

Effects of ooplasm manipulation on DNA methylation and growth of progeny in mice.

Yong Cheng, Kai Wang, Lori D Kellam, Young S Lee, Cheng-Guang Liang, Zhiming Han, Namdori R Mtango, Keith E Latham

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  13. The role of mitochondria from mature oocyte to viable blastocyst.Obstetrics and gynecology international · 2013
    Article
  14. Review
  15. Effects of ooplasm transfer on paternal genome function in mice.Human reproduction (Oxford, England) · 2009
    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

8 authors at 1 institution in 1 country.

Yong ChengThe Fels Institute for Cancer Research and Molecular Biology, Temple University Medical School, Philadelphia, Pennsylvania, USA.
Kai Wang
Lori D Kellam
Young S Lee
Cheng-Guang Liang
Zhiming Han
Namdori R Mtango
Keith E Latham
Temple University · US

Funding

The Primate Embryo Gene Expression ResourceR24RR015253 · NCRR · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2000 to 2011
$4.9M
Epigenetic Effect of Ooplasm Manipulation on DevelopmentR01RR018907 · NCRR · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2004 to 2008
$1.8M
Preimplantation Embryo Blastomere FragmentationR01HD041440 · NICHD · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2002 to 2006
$1.6M
NCRR NIH HHS R01 RR018907NCRR NIH HHS R01 RR18907NCRR NIH HHS R24 RR015253NCRR NIH HHS R24 RR15253NICHD NIH HHS R01 HD041440NICHD NIH HHS R01 HD41440
6 · The paper itself

Abstract

New techniques to boost male and female fertility are being pioneered at a rapid pace in fertility clinics to increase the efficiency of assisted reproduction methods in couples in which natural conception has not been achieved. This study investigates the possible epigenetic effects of ooplasm manipulation methods on postnatal growth and development using a mouse genetic model, with particular emphasis on the possible effects of intergenotype manipulations. We performed interstrain and control intrastrain maternal pronuclear transfers, metaphase-II spindle transfers, and ooplasm transfer between C57BL/6 and DBA/2 mice, and found no major, long-term growth defects or epigenetic abnormalities, in either males or females, associated with intergenotype transfers. Ooplasm transfer itself was associated with reduced viability, and additional subtle effects of ooplasm strain of origin were observed. Both inter- and intrastrain ooplasm transfer were associated with subtle, transient effects on growth early in life. We also performed inter- and intrastrain germinal vesicle transfers (GVTs). Interstrain GVT females, but not males, had significantly lower body weights at birth and thereafter compared with the intrastrain GVT and non-GVT controls. No GVT-associated changes were observed in DNA methylation of the Mup1, Rasgrf1, H19, Snrpn, or Peg3 genes, nor any difference in expression of the imprinted Rasgrf1, Igf2r, or Mest genes. These results indicate that some ooplasm manipulation procedures may exert subtle effects on growth early in life, while intergenotype GVT can result in significant growth deficiencies after birth.

Indexed as

Zygote Intrafallopian TransferAnimalsAnimals, NewbornCytoplasmDNA MethylationEmbryo Culture TechniquesEpigenesis, GeneticFemaleKruppel-Like Transcription FactorsMiceMice, Inbred C57BLMice, Inbred DBAModels, AnimalOocytesProteinsras-GRF1Kruppel-Like Transcription Factorsmajor urinary proteinsPeg3 protein, mouseProteinsras-GRF1Rasgrf1 protein, mouse

Identifiers

PMID19073997
PMCPMC2805397
OpenAlexW2148196686

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.