The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Placental-specific IGF-II is a major modulator of placental and fetal growth
Abstract
Imprinted genes in mammals are expressed from only one of the parental chromosomes, and are crucial for placental development and fetal growth. The insulin-like growth factor II gene (Igf2) is paternally expressed in the fetus and placenta. Here we show that deletion from the Igf2 gene of a transcript (P0) specifically expressed in the labyrinthine trophoblast of the placenta leads to reduced growth of the placenta, followed several days later by fetal growth restriction. The fetal to placental weight ratio is thus increased in the absence of the P0 transcript. We show that passive permeability for nutrients of the mutant placenta is decreased, but that secondary active placental amino acid transport is initially upregulated, compensating for the decrease in passive permeability. Later the compensation fails and fetal growth restriction ensues. Our study provides experimental evidence for imprinted gene action in the placenta that directly controls the supply of maternal nutrients to the fetus, and supports the genetic conflict theory of imprinting. We propose that the Igf2 gene, and perhaps other imprinted genes, control both the placental supply of, and the genetic demand for, maternal nutrients to the mammalian fetus.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Comparison of the placental-specific Igf2P0 with the complete Igf2 null mutant demonstrates clearly that the small placenta can become more efficient by increasing its nutrient transfer and transporter abundance when there is a maintained drive for growth by feto-placental tissues still expressing Igf2 (124, 125).”
From Placental Origins of Chronic Disease (2016) · cites this paper as [125]
Citations
Cites
Role of insulin-like growth factors in embryonic and postnatal growth
Baker, J., Liu, J.-P., Robertson, E. J., & Efstratiadis, A. (1993) · Cell · doi:10.1016/s0092-8674(05)80085-6 · Cited by 2,463
Genomic imprinting: parental influence on the genome
Reik, W., & Walter, J. (2001) · Nature Reviews Genetics · doi:10.1038/35047554 · Cited by 2,288
Self-citationParental imprinting of the mouse insulin-like growth factor II gene
DeChiara, T. M., Robertson, E. J., & Efstratiadis, A. (1991) · Cell · doi:10.1016/0092-8674(91)90513-x · Cited by 1,804
Genomic imprinting in mammalian development: a parental tug-of-war
Moore, T. (1991) · Trends in Genetics · doi:10.1016/0168-9525(91)90230-n · Cited by 1,281
Fetal programming and adult health
Godfrey, K. M., & Barker, D. J. P. (2001) · Public Health Nutrition · doi:10.1079/phn2001145 · Cited by 987
Disruption of imprinting caused by deletion of the H19 gene region in mice
Leighton, P. A., Ingram, R. S., Eggenschwiler, J. T., Efstratiadis, A., & Tilghman, S. M. (1995) · Nature · doi:10.1038/375034a0 · Cited by 756
Nielsen, J., Christiansen, J., Lykke-Andersen, J., Johnsen, A. H., Wewer, U. M., & Nielsen, F. C. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.2.1262 · Cited by 721
Lau, M. M., Stewart, C. E., Liu, Z., Bhatt, H., Rotwein, P. S., & Stewart, C. L. (1994) · Genes & Development · doi:10.1101/gad.8.24.2953 · Cited by 607
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
Lefebvre, L., Viville, S., Barton, S. C., Ishino, F., Keverne, E. B., & Surani, M. A. (1998) · Nature Genetics · doi:10.1038/2464 · Cited by 561
Regulation of Maternal Behavior and Offspring Growth by Paternally Expressed Peg3
Li, L.-L., Keverne, E. B., Aparicio, S. A. J. R., Ishino, F., Barton, S. C., & Surani, M. A. (1999) · Science · doi:10.1126/science.284.5412.330 · Cited by 512
The Sins of the Fathers and Mothers
Tilghman, S. M. (1999) · Cell · doi:10.1016/s0092-8674(00)80559-0 · Cited by 482
Regulation of embryonic growth and lysosomal targeting by the imprintedIgf2/Mpr gene
Wang, Z., Fung, M. R., Barlow, D. P., & Wagner, E. F. (1994) · Nature · doi:10.1038/372464a0 · Cited by 472
Imprinting and the Epigenetic Asymmetry Between Parental Genomes
Ferguson‐Smith, A. C., & Surani, M. A. (2001) · Science · doi:10.1126/science.1064020 · Cited by 405
Self-citationGenomic imprinting of Mash2, a mouse gene required for trophoblast development
Guillemot, F., Caspary, T., Tilghman, S. M., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., Anderson, D. J., Joyner, A. L., Rossant, J., & Nagy, A. (1995) · Nature Genetics · doi:10.1038/ng0395-235 · Cited by 369
Transactivation of Igf2 in a mouse model of Beckwith–Wiedemann syndrome
Sun, F.-L., Dean, W., Kelsey, G., Allen, N. D., & Reik, W. (1997) · Nature · doi:10.1038/39797 · Cited by 331
Self-citationPhenotypic alterations in insulin-deficient mutant mice
Duvillié, B., Cordonnier, N., Deltour, L., Dandoy‐Dron, F., Itier, J., Monthioux, E., Jami, J., Joshi, R. L., & Bucchini, D. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.10.5137 · Cited by 272
Moore, T., Constância, M., Zubair, M., Bailleul, B., Feil, R., Sasaki, H., & Reik, W. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.23.12509 · Cited by 255
Self-citationDeletion of a silencer element in Igf2 results in loss of imprinting independent of H19
Constância, M., Dean, W., Lopes, S. M. C. D. S., Moore, T., Kelsey, G., & Reik, W. (2000) · Nature Genetics · doi:10.1038/79930 · Cited by 200
Self-citationThe long-term consequences of intra-uterine protein malnutrition for glucose metabolism
Ozanne, S. E., & Hales, C. N. (1999) · Proceedings of The Nutrition Society · doi:10.1017/s0029665199000804 · Cited by 192
Sun, T., & Ying, J. Y. Y. (1997) · Nature · doi:10.1038/39549 · Cited by 179
Roles for genomic imprinting and the zygotic genome in placental development
Georgiades, P., Watkins, M., Burton, G. J., & Ferguson‐Smith, A. C. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081540898 · Cited by 140
Self-citationNeutral amino acid transport systems of microvillous membrane of human placenta
Johnson, L. W., & Smith, C. (1988) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1988.254.6.c773 · Cited by 130
Physiological importance of system A-mediated amino acid transport to rat fetal development
Cramer, S., Beveridge, M. J., Kilberg, M. S., & Novak, D. A. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2002.282.1.c153 · Cited by 97
Burns, J. L., & Hassan, A. B. (2001) · Development · doi:10.1242/dev.128.19.3819 · Cited by 86
The uniqueness of the imprinting mechanism
Sleutels, F., Barlow, D. P., & Lyle, R. (2000) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(00)00062-9 · Cited by 84
Hill, D. J. (1990) · Early Human Development · doi:10.1016/0378-3782(90)90110-5 · Cited by 61
Imprinted Genes and the Coordination of Fetal and Postnatal Growth in Mammals
Reik, W., Davies, K., Dean, W., Kelsey, G., & Constância, M. (2001) · Novartis Foundation symposium · doi:10.1002/0470846666.ch3 · Cited by 59
Self-citationAdam, G., Cui, H., Miller, S. J., FLAM, F., & OHLSSON, R. I. (1996) · Development · doi:10.1242/dev.122.3.839 · Cited by 58
Gardner, R. L., Squire, S. E., Zaina, S., Hills, S., & Graham, C. F. (1999) · Biology of Reproduction · doi:10.1095/biolreprod60.1.190 · Cited by 45
Discriminating translation of insulin‐like growth factor‐II (IGF‐II) during mouse embryogenesis
Newell, S., Ward, A., & Graham, C. (1994) · Molecular Reproduction and Development · doi:10.1002/mrd.1080390302 · Cited by 25
Atkinson, D. E., Robinson, N. R., & Sibley, C. P. (1991) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1991.261.6.r1461 · Cited by 18
Self-citation
Cited by
Sorted by citations
Early Developmental Conditioning of Later Health and Disease: Physiology or Pathophysiology?
Hanson, M. A., & Gluckman, P. D. (2014) · Physiological Reviews · doi:10.1152/physrev.00029.2013 · Cited by 1,188
Placental Origins of Chronic Disease
Burton, G. J., Fowden, A. L., & Thornburg, K. L. (2016) · Physiological Reviews · doi:10.1152/physrev.00029.2015 · Cited by 717
Self-citationNongenetic Inheritance and Its Evolutionary Implications
Bonduriansky, R., & Day, T. (2009) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev.ecolsys.39.110707.173441 · Cited by 731
Endocrine Regulation of Human Fetal Growth: The Role of the Mother, Placenta, and Fetus
Murphy, V. E., Smith, R., Giles, W. B., & Clifton, V. L. (2006) · Endocrine Reviews · doi:10.1210/er.2005-0011 · Cited by 673
The Placenta Is a Niche for Hematopoietic Stem Cells
Gekas, C., Dieterlen‐Lièvre, F., Orkin, S. H., & Mikkola, H. K. A. (2005) · Developmental Cell · doi:10.1016/j.devcel.2004.12.016 · Cited by 689
Metadata
- Authors
- Constância, M., Hemberger, M., Hughes, J., Dean, W., Ferguson-Smith, A., Fundele, R., Stewart, F., Kelsey, G., Fowden, A., Sibley, C., & Reik, W.
- Affiliations
- Babraham Institute (GB)
- University of Calgary (CA)
- Max Planck Society (DE)
- University of Cambridge (GB)
- University of Manchester (GB)
- Corresponding author
- Constância, Miguel
- Reik, Wolf
- ORCID
- Venue
- Nature
- Published
- 2002-06
- Volume
- 417
- Issue
- 6892
- Pages
- 945-948
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2092668546
- Cited by
- 1,054
- References
- 31
- Citations by year
- 2026: 15 · 2025: 20 · 2024: 32 · 2023: 42 · 2022: 37 · 2021: 37 · 2020: 36 · 2019: 46 · 2018: 38 · 2017: 42 · 2016: 45 · 2015: 46 · 2014: 41 · 2013: 50 · 2012: 70
- FWCI
- 24.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Medical Research Council
- Biotechnology and Biological Sciences Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Syndromes and Imprinting
- Health Sciences › Medicine › Obstetrics and Gynecology › Pregnancy and preeclampsia studies
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Keywords
- insulin-like growth factor II, genomic imprinting, placental development, fetal growth restriction, amino acid transport
- MeSH terms
- Alleles, Animals, Biological Transport, Female, Embryonic and Fetal Development, Fetus, Gestational Age, Insulin-Like Growth Factor II, Kinetics, Male, Maternal-Fetal Exchange, Organ Specificity, Permeability, Placenta, Placentation, Pregnancy, RNA, Messenger, Trophoblasts, Gene Deletion, In Situ Hybridization, Mice, Knockout, Genomic Imprinting, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review