Summary: Researchers discovered that unborn babies utilize a paternal gene to manipulate their mother’s metabolism, securing more nutrients during pregnancy.
This “remote control” triggers a maternal-fetal tug of war over resources. The study examined the placental hormones that instruct mothers to accommodate their baby’s growth. It’s the first direct evidence that a father’s gene influences the mother to redirect nutrients to the fetus.
Key Facts:
- The study provides the first direct evidence of a gene inherited from the father signalling the mother to divert nutrients to the fetus.
- Scientists deleted the expression of an imprinted gene called Igf2, discovering that without its function, mothers do not make enough glucose and fats available for the fetus, resulting in insufficient fetal growth.
- Babies with Igf2 gene defects can be either overgrown or growth-stunted, affecting their lifelong health and potentially leading to diabetes and obesity in later life.
Source: St. John’s College, University of Cambridge
Unborn babies use ‘greedy’ gene from dads to ‘remote-control’ mums into feeding them extra food
Fetuses use a copy of a gene inherited from their dad to force their mum to release as much nutrients as possible during pregnancy, Cambridge scientists have discovered.
The unborn baby ‘remote controls’ its mother’s metabolism so the two are in a nutritional tug of war. The mother’s body wants the baby to survive but needs to keep enough glucose and fats circulating in her system for her own health, to be able to deliver the baby, breastfeed and to reproduce again.
A new study from the University of Cambridge published today examines how the placenta communicates with the mother through the release of hormones so she will accommodate her baby’s growth.
The placenta is a vital organ that develops with the fetus in pregnant women and other female mammals to support the developing fetus. In pregnant mice, scientists selectively altered the signalling cells in the placenta that tell mothers to allocate nutrients to her developing fetuses.
Professor Amanda Sferruzzi-Perri, Professor in Fetal and Placental Physiology, a Fellow of St John’s College and co-senior author of the paper, said: “It’s the first direct evidence that a gene inherited from the father is signalling to the mother to divert nutrients to the fetus.”
Dr Miguel Constancia, MRC Investigator based at the Wellcome-MRC Institute of Metabolic Science and co-senior author of the paper, said: “The baby’s remote control system is operated by genes that can be switched on or off depending on whether they are a ‘dad’s’ or ‘mum’s’ gene’, the so-called imprinted genes.
“Genes controlled by the father are ‘greedy’ and ‘selfish’ and will tend to manipulate maternal resources for the benefit of the fetuses, so to grow them big and fittest. Although pregnancy is largely cooperative, there is a big arena for potential conflict between the mother and the baby, with imprinted genes and the placenta thought to play key roles.”
The findings by researchers from the Centre for Trophoblast Research at Cambridge’s Department of Physiology, Development and Neuroscience and the Medical Research Council Metabolic Diseases Unit, part of the Wellcome-MRC Institute of Metabolic Science, have been published in Cell Metabolism.
The baby’s genes controlled by the father tend to promote fetal growth and those controlled by the mother tend to limit fetal growth.
Professor Sferruzzi-Perri explained: “Those genes from the mother that limit fetal growth are thought to be a mother’s way of ensuring her survival, so she doesn’t have a baby that takes all the nutrients and is too big and challenging to birth.
“The mother also has a chance of having subsequent pregnancies potentially with different males in the future to pass on her genes more widely.”
Researchers deleted the expression of an important imprinted gene called Igf2, which provides instructions for making a protein called ‘Insulin Like Growth Factor 2’.
Similar to the hormone insulin, which is responsible for making and controlling glucose levels in our circulation, the gene promotes fetal growth and plays a key part in the development of fetal tissues including the placenta, liver and brain.
Dr Jorge Lopez-Tello, a lead author of the study based at the University’s Department of Physiology, Development and Neuroscience, said: “If the function of Igf2 from the father is switched off in signalling cells, the mother doesn’t make enough amounts of glucose and lipids – fats – available in her circulation. These nutrients therefore reach the fetus in insufficient amounts and the fetus doesn’t grow properly.”
The scientists found that deleting Igf2 from the placenta’s signalling cells affects the production of other hormones that modulate the way the mother’s pancreas produces insulin, and how her liver and other metabolic organs respond.
“We found Igf2 controls the hormones responsible for reducing insulin sensitivity in the mother during pregnancy. It means the mother’s tissues don’t absorb glucose so nutrients are more available in the circulation to be transferred to the fetus,” said Professor Sferruzzi-Perri.
Babies with Igf2 gene defects can be overgrown or growth-stunted. “Until now, we didn’t know that part of the Igf2 gene’s role is to regulate signalling to the mother to allocate nutrients to the fetus,” added Professor Sferruzzi-Perri.
The mice studied were smaller at birth and their offspring showed early signs of diabetes and obesity in later life.
Professor Sferruzzi-Perri said: “Our research highlights how important the controlled allocation of nutrients to the fetus is for the lifelong health of the offspring, and the direct role the placenta plays.
“The placenta is an amazing organ. At the end of pregnancy, the placenta is delivered by the mother, but the memories of how the placenta was functioning leaves a lasting legacy on the way those fetal organs have developed and then how they’re going to function through life.”
The next step is to understand how placental hormones are controlled by Igf2 and what those hormones are doing. Future research could help scientists discover new strategies to target the placenta to improve health outcomes for mums and babies.
About this genetics and neurodevelopment research news
Author: Jo Tynan
Source: St. John’s College, University of Cambridge
Contact: Jo Tynan – St. John’s College, University of Cambridge
Image: The image is credited to Neuroscience News
Original Research: Open access.
“Fetal manipulation of maternal metabolism is a critical function of the imprinted Igf2 gene” by Amanda Sferruzzi-Perriet al. Cell Metabolism
Abstract
Fetal manipulation of maternal metabolism is a critical function of the imprinted Igf2 gene
Highlights
- Placenta endocrine cell (Jz) IGF2 loss impairs maternal adaptation in pregnant mice
- Jz IGF2 loss reduces maternal glucose and lipid availability for fetal growth
- IGF2 regulates metabolism, protein synthesis, and hormone secretion of Jz cells
- Lack of Jz IGF2 programs offspring for postnatal metabolic dysfunction
Summary
Maternal-offspring interactions in mammals involve both cooperation and conflict. The fetus has evolved ways to manipulate maternal physiology to enhance placental nutrient transfer, but the mechanisms involved remain unclear. The imprinted Igf2 gene is highly expressed in murine placental endocrine cells.
Here, we show that Igf2 deletion in these cells impairs placental endocrine signaling to the mother, without affecting placental morphology. Igf2 controls placental hormone production, including prolactins, and is crucial to establish pregnancy-related insulin resistance and to partition nutrients to the fetus.
Consequently, fetuses lacking placental endocrine Igf2 are growth restricted and hypoglycemic. Mechanistically, Igf2 controls protein synthesis and cellular energy homeostasis, actions dependent on the placental endocrine cell type. Igf2 loss also has additional long-lasting effects on offspring metabolism in adulthood.
Our study provides compelling evidence for an intrinsic fetal manipulation system operating in placenta that modifies maternal metabolism and fetal resource allocation, with long-term consequences for offspring metabolic health.
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