U.S. Department of Health and Human Services
Lee Weinstein
 

 Contact Info

 
Tel: +1 301 402 2923
Email: leew@mail.nih.gov
 

 Training and Experience

 
M.D., Columbia University College of Physicians and Surgeons, 1983

B.S., Massachusetts Institute of Technology, 1979
 

 Related Links

 

    Specialties: Molecular Biology/Biochemistry, Genetics/Genomics, Endocrinology

    Research Summary

    Research Goal

    Our ultimate goal is to understand the role that the G protein, Gsα, plays in the development of obesity in children with PHP1a and more generally the role of Gsα and other G proteins in the regulation of energy balance and glucose metabolism.  With this insight, we can potentially design therapeutic targets for obesity and diabetes.

    Current Research

    Our laboratory studies the genetic regulation, biochemistry, and physiological roles of the heterotrimeric G protein Gs, which is required for hormone-stimulated intracellular cAMP accumulation and other G proteins, with a particular focus on the role of these G proteins in regulation of energy and glucose homeostasis.  Using the human genetic model Albright hereditary osteodystrophy (AHO), which is associated with heterozygous inactivating mutations in the Gsα-subunit gene (GNAS), and a mouse model with heterozygous inactivation of Gnas, we have demonstrated that Gsα is imprinted in a tissue-specific manner with the paternal allele poorly expressed in some tissues.  This most likely explains why maternal transmission of AHO leads to multihormone resistance and obesity (pseudohypoparathyroidism type 1a, PHP1a) while paternal transmission does not (pseudopseudohypoparathyroidism, PPHP).  We have identified an imprint control region for Gsα and have shown that imprinting (methylation) of this region is abnormally imprinted in pseudohypoparathyroidism type 1b, an isolated form of hormone resistance.  We recently showed that maternal Gsα mutations also lead to obesity and insulin-resistant diabetes in mice and that this parent-of-origin effect of Gsα mutations on energy balance and glucose metabolism is due to Gsα imprinting within the central nervous system.  We are presently trying to define the specific areas within the central nervous system where this effect lies and the underlying signaling mechanisms involved.  We are also conducting detailed metabolic studies in PHP1a and related patients in the Clinical Center’s Metabolic Unit.​

    Applying our Research

    Understanding the mechanisms by which energy balance and glucose metabolism are regulated by the central nervous system is fundamental in helping design future medications for the treatment of obesity and diabetes, two conditions with very significant morbidity and mortality rates and with an ever-increasing prevalence in the general population.

    Need for Further Study

    We need to understand in which areas of the brain Gsα is affected by genomic imprinting and how Gsα deficiency in these regions leads to such profound metabolic effects.