Mothers leave their mark on their children in many ways – and WEHI researchers have discovered a protein called SMCHD1 is involved in this ‘imprinting’ process.
(L-R) Professor Marnie Blewitt, Dr Quentin Gouil and Ms Iromi Wanigasuriya have uncovered a new way that mothers can impact gene expression in their children.
SMCHD1 switches certain genes off, altering how a cell behaves. The new research has revealed that when an egg cell (or oocyte) is fertilised by a sperm, the egg cell’s SMCHD1 lingers within the developing embryo, switching off at least 10 different genes and impacting the embryo’s development – which could potentially have a lifelong impact on the offspring.
Some genes have different expression, depending on whether they have been inherited from the mother or father – a phenomenon called genomic imprinting
WEHI researchers have discovered that the protein SMCHD1 is involved in genomic imprinting, with protein from the mother lingering in an embryo and switching ten genes off
The discovery sheds new light on how genomic imprinting occurs, and may reveal new clues to how SMCHD1 contributes to certain developmental and degenerative disorders.
Imprinted genes
SMCHD1 researcher Ms Iromi Wanigasuriya
We inherit all our genes from our parents – and there are a few genes that behave differently in offspring, depending on whether they are inherited from the mother or the father. This phenomenon is called ‘genomic imprinting’, and is seen in some genetic diseases, said Ms Wanigasuriya, who undertook the research as a PhD student at WEHI.
“Genomic imprinting occurs because of ‘epigenetic marks’ on DNA that impact how genes can be used,” she said. “When a sperm fertilises an egg, both cells’ DNA carries epigenetic marks from the parent to the child, which in some cases have been linked to long-term health impacts,” she said. “It is known that proteins found within the egg (proteins that we get from our mum) help to protect these imprinted genes during early embryo development. Therefore, these egg cell proteins can have either a long or a short-term impact on the health of the embryo.”.
Professor Blewitt’s research team has been studying the SMCHD1 protein, which uses epigenetic modification to ‘switch off’ or silence certain genes.
SMCHD1 produced by the mother (green) can be seen remaining in embryos as the cells divide. WEHI’s researchers have revealed this can impact gene expression in the embryo, in an example of ‘genomic imprinting’.
“We investigated whether a mother’s SMCHD1 protein could be transferred into a newly formed embryo, and how this impacted the expression of imprinted genes,” Ms Wanigasuriya said. “Using advanced microscopy to follow a fluorescently tagged version of SMCHD1, we could see that the maternal SMCHD1 protein persisted within embryos for at least five cell divisions. The mother’s SMCHD1 altered the imprinted gene expression – potentially leaving a lasting legacy in the offspring.”
Understanding SMCHD1
(L-R) Dr Quentin Gouil, Professor Marnie Blewitt and Associate Professor Matthew Ritchie, pictured in 2019
Dr Gouil said the research revealed a critical window of time in early embryonic development during which the mother’s SMCHD1 could silence the expression of target genes.
“Using powerful new genomic analysis techniques, we were able to identify ten genes that were switched off by maternal SMCHD1 in the early embryo. This is the first time SMCHD1 from the egg has been identified as having a role in imprinting,” he said.
“While the effects we discovered were subtle, we know that events occurring in early embryonic development can have long-term effects on health. As well as extending our understanding of genomic imprinting, this research adds an extra dimension to the many ways we know parents can impact their offspring’s health.”
Professor Blewitt said the research also helped to explain recently discovered roles of SMCHD1 in certain diseases including developmental disorders such as Prader-Willi Syndrome (PWS) and Bosma arhinia microphthalmia syndrome (BAMS), as well as facioscapulohumeral muscular dystrophy (FSHD), a form of muscular dystrophy.
“Studying SMCHD1 in early embryos has uncovered new gene targets that this protein silences,” she said. “This could explain how changes in SMCHD1 activity contribute to diseases. We are currently leading a proprietary drug discovery effort at WEHI to leverage our knowledge around SMCHD1 and design novel therapies to treat developmental and degenerative disorders. This research broadens our understanding of how these novel drug candidates might impact gene expression.”
WEHI is open to enquiries from prospective industry partners and investors for the future co-development of these novel therapies towards clinical and market stages. Learn more.
This research was supported by the Australian National Health and Medical Research Council, the Bellberry-Viertel Senior Medical Research Fellowship and the Victorian Government.
WEHI Authors: Ms Iromi Wanigasuriya, Dr Quentin Gouil, Dr Sarah Kinkel, Mr Andrés Tapia del Fierro, Ms Tamara Beck, Ms Kelsey Breslin, Dr Andrew Keniry, Associate Professor Matthew Ritchie, Professor Marnie Blewitt
