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Research

Lactation is a fundamental characteristic of mammals, providing essential nutrient-rich milk that supports infant growth and development. Beyond nutrition, within the breastmilk lies a blueprint for healthy life course trajectories and disease prevention for mothers and infants.

Breastfeeding benefits maternal health, by reducing the risks of breast and ovarian cancer, postpartum depression and by promoting mother-offspring bonding through oxytocin and dopamine release. For infants, breastmilk provides tailored nutrition, immune protection, reduces morbidity, and lowers the risk of obesity and diabetes, while also holding societal and evolutionary significance. Despite its importance, much about the mechanisms behind postnatal nutrition remains unknown.

Our research seeks to illuminate these mechanisms by studying lactation through an integrative lens. Unlike traditional studies, which often focus on cancer or human milk composition alone, our holistic approach examines the mother, offspring, and milk as an integrated system to uncover the mechanisms regulating lactation.

A significant focus of this work is on imprinted genes, which are crucial for embryonic and placental development but remain largely unexplored in relation to mammary gland function. We also explore maternal inter-organ communication involving the mammary gland, both sending and receiving signals, to better understand how lactation is coordinated at the whole-organism level.

Research aims:

  1. Explore maternal inter-organ communication between the mammary gland, the placenta and other maternal organs, to understand how these signals influence lactation and maternal health.
  2. Investigate the function of candidate imprinted genes on mammary gland development, lactation and offspring growth.
  3. Study imprinted gene protein products in human breastmilk.

Publications

Key publications: 

Alsulaiti B, Ferguson-Smith AC, Hanin G (2025) From Mammary Glands to Nutrients: Genetic Insights into Milk Composition. Biology of Reproduction
 

Hanin G, Costello KR, Tavares H, Alsulaiti B, Patel S, Edwards CA, Ferguson-Smith AC (2024).  Dynamic allelic expression in mouse mammary gland across the adult developmental cycle. bioRxiv preprint, in revision DOI: https://doi.org/10.1101/2024.09.02.610775
 

Hanin G, Alsulaiti B, Costello KR, Tavares H, Takahashi N, Mikheeva LA, Freeman AK, Patel S, Jenkins B, Koulman AK, Ferguson-Smith AC (2023).  ZFP57 is a regulator of postnatal growth and life-long healthbioRxiv preprint, in revision DOI: 10.1101/2023.08.27.554997v1
 

Hanin G, Ferguson-Smith AC (2023) Mammary adipocyte flow cytometry as a tool to study mammary gland biology. FEBS open bio. DOI: 10.1002/2211-5463.13620
 

Hanin G, Ferguson-Smith AC (2020) The evolution of genomic imprinting: Epigenetic control of mammary gland development and post-natal resource control. Wiley Interdisciplinary Reviews: Systems Biology and Medicine: e1476. DOI: 10.1002/wsbm.1476.
 

Hanin G, Yayon N, Tzur Y, Haviv R, Bennett E.R, Udi S, Krishnamoorthy Y.R., Kotsiliti E, Zangen R, Efron B, Tam J, Pappo O, Shteyer E, Pikarsky E, Heikenwalder M, Greenberg, D.S., Soreq H (2018) MiRNA-132 induces hepatic steatosis and hyperlipidaemia by synergistic multi-target suppression. Gut, 67:1124-1134. DOI: 10.1136/gutjnl-2016-312869
 

Hanin G, Shenhar-Tsarfaty S, Yayon N, Yau YH, Bennett ER, Sklan EH, DC Rao, Rankinen T, Bouchard C, Geifman-Shochat S, Shifman S, Greenberg DS, and Soreq H (2014). Competing targets of microRNA-608 affect anxiety and hypertension. Human Molecular Genetics (17); 4569-80.  DOI: 10.1093/hmg/ddu170

Group Leader, Department of Physiology, Development and Neuroscience
Takes PhD students

Affiliations

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