Evidence map›Paper›PMID 22729990›Full record

ArticleMolecular reproduction and development2012

Plac1 (placenta-specific 1) is essential for normal placental and embryonic development.

Suzanne M Jackman, Xiaoyuan Kong, Michael E Fant

Open access · greenAbstract read
In one paragraph

Article in Molecular reproduction and development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

47 citing papers in PubMed, 79 citations in OpenAlex.

  1. Transcriptomic Analysis ofInternational journal of molecular sciences · 2026
    Article
  2. Transcriptomic Analysis ofbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
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  7. Plac1Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  8. Article
  9. Article
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  11. Placenta: an old organ with new functions.Frontiers in immunology · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Article
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  17. Article
  18. An Overview of the Role of Long Non-Coding RNAs in Human Choriocarcinoma.International journal of molecular sciences · 2021
    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

3 authors at 1 institution in 1 country.

Suzanne M JackmanDepartment of Pediatrics, University of South Florida Morsani College of Medicine, Tampa, FL, USA.
Xiaoyuan Kong
Michael E Fant
University of South Florida · US

Funding

PLAC1 in Placental DevelopmentR21HD048862 · NICHD · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FANT, MICHAEL E. · 2006 to 2007
$326k
NICHD NIH HHS HD048862NICHD NIH HHS R21 HD048862
6 · The paper itself

Abstract

Plac1 is a recently identified, X-linked gene whose expression is restricted primarily to cells of the trophoblast lineage. It localizes to a chromosomal locus previously implicated in placental growth. We therefore sought to determine if Plac1 is necessary for placental and embryonic development by examining a mutant mouse model. Plac1 ablation resulted in placentomegaly and mild intrauterine growth retardation (IUGR). At E16.5, knockout (KO) and heterozygous (Het) placentae of the Plac1-null allele inherited from the mother (X(m-) X) weighed approximately 100% more than wildtype (WT) placentae, whereas the corresponding embryos weighed 7-12% less. Histologically, Plac1 mutants exhibited an expanded spongiotrophoblast layer that invaded the labyrinth. By contrast, Het placentae that inherited the null allele from the father (XX(p-) ) exhibited normal growth and were histologically indistinguishable from WT placentae, consistent with paternal imprinting of Plac1. When examined across gestation, WT and X(m-) X placental weights peaked at E16.5 and decreased slightly thereafter. KO placentae (X(m-) X(p-) and X(m-) Y), however, continued to increase in weight after E16.5, consistent with a functional role for the paternal Plac1 allele. Subsequent analysis confirmed that the paternal allele partially escapes complete X-inactivation and thus contributes to placental growth regulation. Additionally, although male Plac1 KO mice can survive, they exhibit decreased viability as a consequence of events occurring late in gestation or shortly after birth. Thus, Plac1 is a paternally imprinted, X-linked gene essential for normal placental and embryonic development.

Indexed as

AllelesAnimalsChromosomes, MammalianEmbryo, MammalianEmbryonic DevelopmentFemaleGenes, X-LinkedGenomic ImprintingHeterozygoteMaleMiceMice, KnockoutPlacentaPregnancyPregnancy ProteinsX ChromosomePregnancy Proteins

Identifiers

PMID22729990
PMCPMC4594876
OpenAlexW1972401547

What OpenQuestion holds

Textmetadata
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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.