As of January 2010, PRF has provided over $2 million to fund 28 grants for Progeria-related research projects performed in 13 states and 3 other countries! We continue to solicit proposals worldwide and through our scientific workshops, in our continuing effort to encourage researchers to work in this field. All projects are carefully evaluated by our Medical Research Committee and Board of Directors, as we strive to fund research targeted to help us reach our goal of developing treatments and the cure for Progeria. 
Medical Research Grant Application Guidelines [61.5kb PDF]
Medical Research Grant Application Guidelines
Grants We Have Funded and Biological Sketches of the Researchers
-
October 2009: to Jason D. Lieb, PhD, University of North Carolina, Chapel Hill NC
Interactions between genes and lamin A/progerin: a window to understanding Progeria pathology and treatment -
October 2009: To Tom Misteli, PhD, National Cancer Institute, NIH, Bethesda, MD
Identification of small molecule modulators of LMNA splicing -
August 2009: to William L. Stanford, PhD, University of Toronto, Canada
Induced-Pluripotent Stem Cells (iPSC) from HGPS patient fibroblasts to elucidate the molecular mechanism associated with diminishing vascular function -
July 2009: to Jakub Tolar, University of Minnesota, Minneapolis, MN
Correction of human progeria induced pluripotent cells by homologous recombination -
September 2008 (start date January 2009): To Kris Noel Dahl, PhD, Carnegie Mellon University, Pittsburgh, PA
“Quantification of progerin recruitment to membranes” -
October 2007: To Michael A. Gimbrone, Jr., MD, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA Endothelial Dysfunction and the Pathobiology of Accelerated Atherosclerosis in Hutchinson-Gilford Progeria Syndrome
-
September 2007 (Start date January 2008): To Bryce M. Paschal, PhD, University of Virginia School of Medicine, Charlottesville, VA
Nuclear Transport in Hutchinson-Guilford Progeria Syndrome -
May 2007: To Thomas N. Wight, PhD, Benaroya Research Institute, Seattle, WAThe use of a mouse model of HGPS to define the influence of Lamin AD50 expression on vascular extracellular matrix production and the development of vascular disease.
-
March 2007: To Jemima Barrowman, PhD, Johns Hopkins School of Medicine, Baltimore, MD Fundamental Mechanism of Lamin A Processing: Relevance to the Aging Disorder HGPS
- August 2006: To Zhongjun Zhou, PhD, University of Hong Kong, China
Stem cell therapy of Laminopathy-based Premature Aging - August 2006: To Michael Sinensky, PhD, East Tennessee State University, Johnson City, TN
Effect of FTIs’ on the Structure and Activity of Progerin - June 2006: To Jan Lammerding, PhD, Brigham and Women's Hospital, Cambridge, MA
The role of nuclear mechanics and mechanotransduction in Hutchinson-Gilford Progeria syndrome and the effect of farnesyltransferase inhibitor treatment -
June 2006: To Tom Misteli, PhD, National Cancer Institute, NIH, Bethesda, MD
Molecular Therapy Approaches for HGPS via correction of pre-mRNA Splicing -
June 2005: To Lucio Comai, PhD, University of Southern California, Los Angeles, CA
Functional Analysis of Hutchinson-Gilford Progeria Syndrome -
June 2005: To Loren G. Fong, PhD, University of California, Los Angeles, CA
New Mouse Models to Study the Cause of Hutchinson-Gilford Progeria Syndrome -
January 2005: To Dr. Karima Djabali, PhD, Columbia University, New York, New York
Defining progerin dominant negative effects on the nuclear functions in HGPS cells -
December 2004: To Robert D. Goldman, PhD and Dale Shumaker, PhD, Northwestern University Medical School, Chicago, Illinois
The Effects of the Major Mutation on Human Lamin A's Function in DNA Replication -
August 2004 (Start date January 2005): To Stephen Young, PhD, UCLA, Los Angeles, CA, for his project entitled "Genetic Experiments in Mice to Understand Progeria".
-
April 2004: To Monica Mallampalli, Ph D, and Susan Michaelis, PhD, The Johns Hopkins School of Medicine, Baltimore, MD: “Structure, Location and Phenotypic Analysis of Progerin, the mutant form of prelamin A in HGPS”
-
December 2003: To Joan Lemire, PhD, Tufts University School of Medicine, Boston, MA, “Developing a smooth muscle cell model for the study of Hutchinson-Gilford Progeria Syndrome: Is aggrecan a significant component of the phenotype?”
-
December 2003: To W. Ted Brown, MD, PhD, FACMG, The Institute for Basic Research in Developmental Disabilities, Staten Island, NY: “Dominant Negative Mutation Effects of Progerin”
-
September 2003: To Thomas W. Glover, Ph.D., University of Michigan, " Role of Lamin A Mutations in Hutchinson-Gilford Progeria Syndrome"
-
August 2002: To Junko Oshima, MD, PhD, University of Washington, Seattle, WA, for her project entitled, "Cloning of the Gene for Hutchinson-Gilford Progeria Syndrome by Somatic Cell Complementation"
-
May 2002: To Associate Professor Anthony Weiss at the University of Sydney, Australia, Title of project: Candidate Molecular Markers for Hutchinson-Gilford Progeria Syndrome
-
January 2001 (Start date July 2001): To John M. Sedivy, PhD, Brown University, Providence, RI, "Cloning the Gene for Hutchinson-Gilford Progeria Syndrome by Somatic Cell Complementation"
-
December 2001 (Start date February 2002): To Thomas W. Glover, Ph.D., University of Michigan, "Genome Maintenance in Hutchinson-Gilford Progeria Syndrome"
-
January 2000: To Leslie B. Gordon, MD, PhD, Tufts University School of Medicine , Boston, MA, "The Role of Hyaluronic Acid in Hutchinson-Gilford Progeria Syndrome"
-
August 1999: To Leslie B. Gordon, MD, PhD, Tufts University School of Medicine , Boston, MA, "The Pathophysiology of Arterioscleros is in Hutchinson-Gilford Progeria Syndrome"
Medical Research Grant Application Guidelines [61.5kb PDF]
Medical Research Grant Application Guidelines
October 2009: to Jason D. Lieb, PhD, University of North Carolina, Chapel Hill NC
Interactions between genes and lamin A/progerin: a window to understanding Progeria pathology and treatment
Hutchinson–Gilford Progeria Syndrome (HGPS) is caused by a mutation in the lamin A gene, resulting in production of a shortened protein called progerin. Lamin A normally plays an important function in maintaining the organization of the cell nucleus, and the mutation that creates progerin may result in a disorganization that leads to changes in gene regulation, and ultimately HGPS. However, it is not known which genes interact with lamin A in normal cells, or with progerin in the cells of HGPS patients. We hypothesize that abnormal binding or dissociation of genes with lamin A or progerin in HGPS cells causes misregulation of genes, ultimately leading to HGPS. To find which genes interact with normal lamin A and progerin across the entire genome, Dr. Lieb will perform a technique called ChIP-seq. First, he aims to identify genes that abnormally bind to or detach from lamin A or progerin in HGPS cells. Second, he will perform ChIP-seq in HGPS cells treated with a farnesyltransferase inhibitor (FTI), which shows partial efficacy in treating HGPS symptoms in mouse models. This experiment will reveal which genes’ interactions remain abnormal even after FTI treatment. The data will allow his team to predict signaling pathways that may be responsible for HGPS and the persistent HGPS symptoms reported in FTI-treated mouse models, and will provide a clue for new drugs and treatments for HGPS patients.
Dr. Lieb is an Associate Professor in the Department of Biology and Carolina Center for Genome Sciences. The projects in his laboratory are united by the scientific goal of understanding relationships between DNA packaging, transcription factor targeting, and gene expression. They use three biological systems: S. cerevisiae (baker's yeast) to address basic molecular mechanisms; C. elegans to test the importance of those mechanisms in a simple multicellular organism; and (3) cell lines and clinical samples to directly interrogate chromatin function in human development and disease. The experiments will be carried out by postdoctoral fellow Dr. Kohta Ikegami, who was trained as a graduate student at the University of Tokyo.
October 2009: To Tom Misteli, PhD, National Cancer Institute, NIH, Bethesda, MD
Identification of small molecule modulators of LMNA splicing
Dr. Misteli and his team are developing novel therapeutic strategies for Progeria. His group’s work focuses on interfering with the production of the progerin protein using highly specific molecular tools and to find novel small molecules to counteract the detrimental effects of progerin in patient cells. These efforts will lead to a detailed cell biological understanding of Progeria cells and bring us closer to a molecularly based therapy for Progeria.
Dr. Misteli is a Senior Investigator at the National Cancer Institute where he heads the Cell Biology of Genomes Group and the NCI Cellular Screening Initiative. He is a member of the NCI Center for Excellence in Chromosome Biology. Dr. Misteli has pioneered technology to analyze the function of genes in living cells and his work has provided fundamental insights into genome function. Dr. Misteli has received numerous national and international awards for his work and he serves in numerous advisory and editorial functions.
August 2009: to William L. Stanford, PhD, University of Toronto, Canada
Induced-Pluripotent Stem Cells (iPSC) from HGPS patient fibroblasts to elucidate the molecular mechanism associated with diminishing vascular function
iPS cells, or Induced pluripotent stem cells are cells that started out as a mature cell type easily obtained and grown in the laboratory, and are treated with biochemical “cues” that signal the cells’ genetic machinery to turn them into immature stem cells. These stem cells are then given additional biochemical “cues” to mature once again, but not into their original cell type. For example, a skin cell (mature) can be first turned into a stem cell (immature) and then turned into a vascular cell (mature). This cutting edge technology is intensely important for Progeria research, where we cannot obtain live human blood vessel, heart and bone cells of children with Progeria for study. The ability to take a Progeria skin cell, grown easily at the PRF Cell and Tissue Bank, and create a Progeria blood vessel cell, will allow us to study heart disease in Progeria in brand new ways.
These cells will be valuable for the purpose of banking and distribution to members of the Progeria research community for basic studies and drug development. Dr. Stanford will develop multiple Progeria iPS cells to model Progeria vascular disease stem cells (VSMC), which are seriously depleted in Progeria.
Dr. Stanford is a Canada Research Chair in Stem Cell Bioengineering & Functional Genomics, and Associate Professor & Associate Director of the Institute of Biomaterials & Biomedical Engineering at the University of Toronto. He is also the co-Scientific Director of the Ontario Human iPS Cell Facility. His laboratory is focused on basic and applied research in stem cell biology, tissue engineering and modeling human disease using mouse mutagenesis and patient-specific iPS cells.
July 2009: to Jakub Tolar, University of Minnesota, Minneapolis, MN
Correction of human progeria induced pluripotent cells by homologous recombination
Dr. Tolar’s lab has shown that allogeneic cellular therapy with mesenchymal stem cells can prolong survival in the Progeria mouse model, suggesting that cellular therapy can be of benefit to children with Progeria. However, the children have abnormal DNA repair and as such are expected to experience significant toxicities with the chemoradiotherapy needed for engraftment of cells from unrelated donors. Therefore, Dr. Tolar will limit such toxicity by developing genetically corrected cells from the Progeria children themselves, combining the novel concept of iPS cells from Progeria patients with the emerging technology for gene correction mediated by zinc finger nucleases. In this manner he aims to establish a platform for clinical translation of safer stem cell gene therapy with progeny cell types of iPS cells as a definitive treatment for children with Progeria.
Dr. Tolar is an Assistant Professor and attending physician at the University of Minnesota in the Divisions of Pediatric Hematology-Oncology and Pediatric Blood and Marrow Transplantation. Dr. Tolar's research focuses on the use of bone marrow-derived stem cells and gene therapy for correction of genetic diseases and improving outcome of blood and marrow transplantation.
September 2008 (start date January 2009): To Kris Noel Dahl, PhD, Carnegie Mellon University, Pittsburgh, PA
“Quantification of progerin recruitment to membranes”
Hutchinson-Gilford Progeria Syndrome (HGPS) arises from an abnormal association of a mutant form of a structural nuclear lamin protein, progerin with the nuclear membrane. However, the nature of this increased association has not been determined. In this project, Dr. Dahl and her collaborators will quantify the differences in membrane association of normal lamin A and progerin using purified proteins and purified membranes. With this system, they can precisely quantify the strength of the protein-membrane interaction, determine physical changes that the membrane undergoes in contact with the protein and examine protein orientation at the interface. Also, this purified system will allow them to manipulate different variables such as membrane composition and solution charge. Some of the hypotheses to be examined are the role of the lipid tail and the charge cluster retained on progerin versus the native lamin A and the effects on membrane interaction. 
Prof. Kris Noel Dahl is an Assistant Professor in the Departments of Chemical Engineering and Biomedical Engineering at Carnegie Mellon University. She obtained her PhD in Chemical Engineering at the University of Pennsylvania and did a Postdoctoral Fellowship in the Department of Cell Biology at Johns Hopkins Medical School. Dr. Dahl's group focuses on the mechanical properties of the nucleus from the molecular to the multicellular level. HGPS is one of several disease types in which mutations and molecular reorganization leads to unique nuclear mechanical properties.
January 2008: To Bryce M. Paschal, PhD, University of Virginia School of Medicine, Charlottesville, VA
Nuclear Transport in Hutchinson-Guilford Progeria Syndrome
As a principle component of the nuclear lamina, lamin A contributes structural plasticity to the nuclear envelope membrane, provides attachment sites for chromatin, and organizes nuclear pore complexes in the membrane. Given this arrangement, we are exploring how defects in the nuclear lamina observed in Hutchinson-Guilford Progeria Syndrome (HGPS) affect the structure and function of the nuclear pore complex. These studies are designed to provide insight into how changes in nuclear architecture contribute to changes in gene expression in HGPS through transport-based mechanisms.
March 2007: To Jemima Barrowman, PhD, Johns Hopkins School of Medicine, Baltimore, MD
Fundamental Mechanism of Lamin A Processing: Relevance to the Aging Disorder HGPS
August 2006: To Zhongjun Zhou, PhD, University of Hong Kong, China
Stem cell therapy of Laminopathy-based Premature Aging
Stem cells are the cells that can self-renew and differentiate into a variety of different cell types. They are important because they replace the worn-out cells in the body and maintain the functional integrity of our body. The various tissues in our bodies are rapidly renewed by stem cells and it is common that stem cells decline in aged people. We hypothesize that potential of stem cells in HGPS patients are compromised and cannot provide enough new cells for the renewal of various tissues, therefore leading to accelerated ageing processes. In this project, Dr. Zhou will use a mouse model for HGPS to test if the number and the functions of stem cells in HGPS mice are declined and whether stem cells (bone marrow) derived from healthy mice will rescue the ageing phenotypes in HGPS mice. He will also investigate how the stem cells are affected in HGPS. This work directly tests the feasibility of a potential therapeutic strategy for laminopathy-based premature aging.
Dr. Zhou is an Associate Professor in the Department of Biochemistry and Faculty of Medicine at the University of Hong Kong and obtained his PhD in Medical Biochemistry from Karolinska Institute, where he also performed his postdoc training in the Institute’s Department of Medical Biochemistry and Biophysics. HI group’s main focus of research is on molecular mechanism of laminopathy-based premature ageing. In collaboration with groups in Spain and Sweden, they have made a Zmpste24 deficient mouse to serve as a mouse model for HGPS. They found that unprocessed prelamin A and truncated prelamin A found in HGPS compromise the recruitment of checkpoint response/repair proteins to damaged DNA, therefore leading to defective DNA repair which in turn contributes to accelerated ageing. Currently, they are investigating if stem cells are affected in HGPS and testing in mice if bone marrow transplantation could rescue, at least partially, the premature ageing phenotypes.
August 2006: To Michael Sinensky, PhD, East Tennessee State University, Johnson City, TN Effect of FTIs’ on the Structure and Activity of Progerin
Hutchinson-Gilford Progeria Syndrome (HGPS) arises from a novel mutation in the gene encoding the protein prelamin A. Normally, prelamin A undergoes a series of biochemical alterations which allow it to form a part of a structure in the nucleus called the nuclear lamina. The mutant prelamin A formed in HGPS (called progerin) is defective in the last of these biochemical alterations leading to accumulation of an intermediate molecule bearing a lipid group referred to as farnesyl . Compounds, called FTIs, which block the formation of this lipid bearing version of progerin have been postulated to be of therapeutic use in the treatment of HGPS. In this proposal we describe tests of the hypothesis that progerin exhibits novelties in its molecular structure that are secondary to adding farnesyl, particularly addition of phosphate. This hypothesis will be tested as will the effects of FTIs on these postulated additions of phosphate
Dr. Sinensky is Professor and Chair in the Department of Biochemistry and Molecular Biology at East Tennessee State University’s Quillen College of Medicine. Between 1987 and 1994 his laboratory, then located at the University of Colorado Health Sciences Center, demonstrated that farnesylation of prelamin A occurred and was the first step in a proteolytic maturation pathway for the molecule. This work grew out of efforts to understand the mechanism of regulation of cholesterol biosynthesis which has also been a significant part of our research program. Since relocating in 1995 to TN, his main research interests have been in the in vitro reconstruction of the prelamin A processing pathway.
June 2006: To Jan Lammerding, PhD, Brigham and Women's Hospital, Cambridge, MA
The role of nuclear mechanics and mechanotransduction in Hutchinson-Gilford Progeria syndrome and the effect of farnesyltransferase inhibitor treatment
Hutchinson-Gilford Progeria Syndrome (HGPS) is caused by mutations in the gene encoding lamin A/C. Dr. Lammerding recently demonstrated that cells lacking lamin A/C are mechanically more fragile and have increased cell death and decreased protective cellular signaling in response to mechanical stimulation. Abnormal mechanical sensitivity in response to blood flow and vessel expansion could render blood vessels more susceptible to atherosclerosis, the leading cause of death in HGPS. Furthermore, increased sensitivity to mechanical stress could also contribute to bone and muscle abnormalities seen in HGPS patients. In this project, Dr. Lammerding will conduct a series of experiments to evaluate if cells from Hutchinson-Gilford Progeria syndrome patients are more susceptible to damage through mechanical stimulation. In addition, Dr. Lammerding.s experiments will test if treatment with farnesyl-transferase inhibitors (FTI), a promising new drug for HGPS, can reverse the mechanical deficiencies in HGPS cells and thus lead to a reversal of some of the tissue-specific disease phenotypes.
Dr. Lammerding is an Instructor at Harvard Medical School serving in the Department of Medicine at Brigham and Women's Hospital. His areas of interest include subcellular biomechanics and the cellular signaling response to mechanical stimulation. In particular, he is focusing on how mutations in nuclear envelope proteins such as lamin can render cells more sensitive to mechanical stress and affect their mechanotransduction signaling. Insights gained from this work can lead to a better understanding of the molecular mechanism underlying laminopathies, a diverse group of diseases including Emery-Dreifuss muscular dystrophy, HGPS, and familial partial lipodystrophy.
June 2006: To Tom Misteli, PhD, National Cancer Institute, NIH, Bethesda, MD
Molecular Therapy Approaches for HGPS via correction of pre-mRNA Splicing
Dr. Misteli and his team are developing novel therapeutic strategies for progeria. His group’s work focuses on interfering with the production of the progerin protein using highly specific molecular tools and to find novel small molecules to counteract the detrimental effects of the progerin protein in patient cells. These efforts will lead to a detailed cell biological understanding of progeria cells and bring us closer to a molecularly based therapy for progeria.
Dr. Misteli is a Senior Investigator at the National Cancer Institute where he heads the Cell Biology of Genomes Group. He is a member of the NCI Center for Excellence in Chromosome Biology. Dr. Misteli has pioneered technology to analyze the function of genes in living cells and his work has provided fundamental insights into genome function. Dr. Misteli has received numerous national and international awards for his work and he serves in numerous advisory and editorial functions.
June 2005: To Lucio Comai, PhD, University of Southern California, Los Angeles, CA
Functional Analysis of Hutchinson-Gilford Progeria Syndrome
Dr. Comai hypothesizes that expression of the mutant Lamin A protein progerin (that causes Progeria) results in premature aging and cardiac disease as a consequence of altered composition and function of Lamin A-containing complexes within the nucleus. To test this hypothesis, he will seek to identify cellular factors that differentially interact with lamin A and progerin. These studies will provide critical information on the molecular defects of Progeria, as we work toward developing treatments at the cellular level.
Dr. Comai is Associate Professor of Molecular Microbiology & Immunology at the USC Keck School of Medicine, and a member of the Keck School’s Institute for Genetic Medicine, Norris Comprehensive Cancer Center and Research Center for Liver Diseases.
June 2005: To Loren G. Fong, PhD, University of California, Los Angeles, CA
New Mouse Models to Study the Cause of Hutchinson-Gilford Progeria Syndrome
Since the discovery of the Progeria gene mutation more than 2 years ago, efforts have gone on in several laboratories to create a mouse that produces the "bad” lamin A (progerin) made in Progeria. Dr. Fong and his colleagues have succeeded in doing this, and now will investigate the effects of mouse progerin on the growth and metabolic properties of cells, the development of atherosclerosis, bone abnormalities and lipodystrophy in the whole animal, and finally to test whether any abnormalities can be reversed by farnesyl transferase inhibitors, at present the leading candidates for treatment of Progeria.
Dr. Fong is an Assistant Adjunct Professor at UCLA, and has joined forces with Dr. Stephen Young, a May 2005 PRF grantee, to tackle this important scientific and medical problem.
January 2005: To Dr. Karima Djabali, PhD, Columbia University, New York, New York
Defining progerin dominant negative effects on the nuclear functions in HGPS cells
Dr. Djabali will conduct a fascinating series of experiments aimed at demonstrating the direct relationship of the genetic defect in Hutchinson Gilford Progeria Syndrome to numerous important binding partners in order to characterize the biological basis of disease in Progeria. This work will provide the basic data needed to lead to potential treatments.
Dr. Djabali is Assistant Professor at the Department of Dermatology at the Columbia University Medical School. She has been involved in molecular genetic studies of genetic related disease, and the fields of molecular biology, cell biology, biochemistry and proteomics.
December 2004: To Robert D. Goldman, PhD and Dale Shumaker, PhD, Northwestern University Medical School, Chicago, Illinois
The Effects of the Major Mutation on Human Lamin A's Function in DNA Replication
Drs. Goldman and Shumaker seek to determine the molecular basis by which the Progeria gene mutations alter nuclear function to cause the premature aging effects seen in children with Progeria. This will shed light on the basic mechanisms responsible for the age-related disorders in the children, information critical to determining ways to combat the progression of the disease.
Stephen Walter Ranson Professor and Chairman of Cell and Molecular Biology at Northwestern University Medical School, Dr Goldman's research has focused on the dynamics of nuclear lamins during cell cycle, examining the relationship between their structure and function. He is an NIH member of Molecular Approaches to Cell Functions and Interactions and serves on the Human Embryonic Stem Cell Advisory Board for the Juvenile Diabetes Foundation. He has worked as an instructor and director in cell and molecular biology at the Marine Biological Laboratory, Woods Hole, Massachusetts.
Dr. Shumaker is a postdoctoral fellow of Cell and Molecular Biology at Northwestern, and has worked with Dr. Goldman studying nuclear lamins since 2001.
August 2004 (Start date January 2005): To Stephen Young, PhD, for his project entitled "Genetic Experiments in Mice to Understand Progeria".
The aim of this research project is to use mouse models to build an intellectual foundation for designing appropriate therapies for Hutchinson-Gilford Progeria Syndrome caused by the accumulation of a mutant prelamin A (frequently called "progerin") within cells. Dr.Young's laboratory will create a mouse model of Progeria and use that model to understand how the genetic change in Progeria leads to heart disease. As concluded from the BMT workshop, the study of mouse models is a critical next-step in the process to discover treatments and the cure for Progeria. Dr. Young writes, "During the past few years, we have created several animal models to explore lamin A/C biology...We are absolutely convinced that thorough analyses of these mouse models will yield insights relevant to the design of therapies for HGPS.
Dr. Young is a Senior Investigator at the J. David Gladstone Institutes, Professor of Medicine at UCSF, and Staff Cardiologist at the San Francisco General Hospital. Dr. Young will direct and oversee the performance of all the proposed studies. Dr. Young is experienced in using genetically modified mice in biomedical research. His research group has generated and examined more than 50 lines of transgenic mice and more than a 20 gene-targeted mice. In recent years, Dr. Young has studied posttranslational protein modifications, and in particular the postisoprenylation processing steps. During the past few years, his laboratory has generated knockout mice for farnesyltransferase, Zmpste24, Icmt, and Rce1, and prenylcysteine lyase.
April 2004: To Monica Mallampalli, Ph D, and Susan Michaelis, PhD: “Structure, Location and Phenotypic Analysis of Progerin, the mutant form of prelamin A in HGPS”
This project aims to define the structure of progerin (the abnormal protein in HGPS), develop a cell culture system that allows them to study localization of progerin; and generate progerin-specific antibodies and aptamers for the analysis of function and distribution of progerin in cells and tissues of HGPS patients. Understanding progerin structure and determining how progerin gives rise to the disease state will help reveal the molecular mechanism of HGPS, facilitating rational approaches for the development of treatments.
Dr. Mallampalli is a Postdoctoral Researcher in the Department of Cell Biology at The Johns Hopkins School of Medicine with Dr. Michaelis, Professor in Cell Biology Biophysics at The Johns Hopkins School of Medicine.
September 2003 : To Thomas W. Glover, Ph.D. for the project entitled, " Role of Lamin A Mutations in Hutchinson-Gilford Progeria Syndrome"
This project addresses the question of why mutations in lamin A lead to the Progeria phenotype. Recently, the gene responsible for HGPS was identified, and HGPS joined a group of syndromes - the laminopathies - all of which have an underlying defect in the lamin A/C gene (LMNA). Virtually all HGPS patients have the same mutation creating an abnormal splice donor site in exon 11 of the LMNA gene. The result of the mis-splicing creates a protein missing 50 amino acids near the C-terminus. The deleted region includes a protein cleavage site that normally removes 18 amino acids including a CAAX box farnesylation site. Our research efforts are now focused on examining the effects of the causative mutation in cell culture models in order to gain a better understanding of the disease and work toward the long-term goal of discovering a cure. To this end, we are examining the effect of mutant lamin A expression on a variety of cellular phenotypes including lamin A localization, cell death, cell cycle, and nuclear morphology. These experiments involve the expression of mutant and normal lamin A from mammalian expression constructs in a variety of cell types, and confirmation by examination of the effects of the native protein in HGPS cell lines. In addition, we are developing an in vitro model for adipogenesis in HGPS, which may provide insight into the lack of subcutaneous fat, and related phenotypes, seen in HGPS patients. Finally, we hypothesize that it may be possible to correct or improve the mutant phenotype by exposing the cells to compounds that inhibit farnesylation. We have obtained a variety of such inhibitors and we are presently examining the effects of these compounds on the HGPS cellular phenotypes.
Dr. Glover is a Professor in the Department of Human Genetics at the University of Michigan with research interests in the molecular basis of human genetic disease and chromosomal instability. He is the author of over 120 research publications and book chapters. His laboratory has worked extensively on chromosome instability at fragile sites and has identified and cloned a number of human disease genes, most recently a gene responsible for hereditary lymphedema, and collaborated in the identification of the lamin A gene responsible for Hutchinson-Gilford Progeria.
December 2003: To Joan Lemire, PhD: “Developing a smooth muscle cell model for the study of Hutchinson-Gilford Progeria Syndrome: Is aggrecan a significant component of the phenotype?”
This project aims to understand the mechanism by which progerin leads to alterations in connective tissues, and most importantly to cardiovascular disease. Children with HGPS die from myocardial infarction, congestive heart failure, and strokes. Aggrecan is a component of connective tissue, and is dramatically elevated in fibroblasts from HGPS patients. Dr. Lemire hypothesizes that this aggrecan overexpression is not limited to fibroblasts and that the arterial smooth muscle cells will also produce aggrecan, which could contribute significantly to this narrowing of the arteries in HGPS. If proven correct, preventing or reversing the lumenal narrowing through aggrecan manipulation may delay the onset of cardiovascular symptoms.
Dr. Lemire is Assistant Professor at Tufts University and recently obtained an NIH-funded grant supporting research in the role of decorin in HGPS.
December 2003: To W. Ted Brown, MD, PhD, FACMG: “Dominant Negative Mutation Effects of Progerin”
To find a potential treatment for HGPS, the mechanism by which the mutated form of lamin A protein, progerin, leads to the disease must be understood. Progerin appears to have a dominant negative mutation; it takes on new functions and produces negative, unwanted effects on cellular functions. Dr. Brown hypothesizes that progerin binds to a key nuclear protein, to which lamin A normally does not bind, and this abnormal binding causes detrimental effects. The project focuses on characterizing this unusual binding to help explain how the mutation leads to HGPS.
Dr. Brown is Chairman of the Department of Human Genetics and Director of the George A Jervis Clinic at the New York State Institute for Basic Research. He is a world expert on Progeria, having studied the syndrome for the past 25 years. His cell banking of a number of Progeria cell lines, and his studies contributed to the eventual identification of LMNA mutations in Progeria.
May 2002: To Associate Professor Anthony Weiss at the University of Sydney
Title of project: Candidate Molecular Markers for Hutchinson-Gilford Progeria Syndrome
Project Description: Accurate diagnosis of Hutchinson-Gilford Progeria Syndrome (HGPS) requires a reliable marker. We have used glyean detection to describe gp200 and identified key overexpressed transcripts that are excellent candidates for HGPS markers in cultured fibroblasts. This one-year project will allow us to use proteomics to identify gp200 and real time RT-PCR methods for examining a leading transcribed candidate marker hgpg200. We will improve the sensitivity of our published gp200 assay, expand the utility of specific transcript analysis, and develop a sensitive assay to facilitate marker detection.
This work is important to children with HGPS. (1) It will aid early and accurate diagnosis. (2) This project marks the first time that this combination of proteomics and microarrays/real time RT-PCR tools is used to explore the molecular features of HGPS. (3) We will identify key molecules that distinguish HGPS. Their identification will provide us with information on the molecular biology and biochemistry of HGPS. (4) By the end of year 1, we expect to provide an assay that can be reliably considered, beyond the current grant, in small biopsy samples and buccal cells taken by gentle swabs.
Biographical Sketch: Tony Weiss is founding Chair of the Molecular Biotechnology Program University of Sydney, Associate Professor of Biochemistry in the School of Molecular and Microbial Biosciences University of Sydney, Honorary Visiting Scientist in Molecular and Clinical Genetics at Royal Prince Alfred Hospital, and Visiting Professor at the National University of Singapore. Tony was given the Roslyn Flora Goulston Prize and an Australian Postgraduate Research Award then made an ARC Postdoctoral Fellow, after which he moved to the USA as a NIH Fogarty International Fellow. He received further awards including a Fulbright Fellowship at Stanford University before returning to Australia as a CSIRO Postdoctoral Scholar to take up a Faculty position at the University of Sydney. He has twice been a Thomas and Ethel Mary Ewing Scholar and was made a Royal Society Exchange Scholar to pursue research studies in the LTK. Tony was recognized by the Australian Society for Biochemistry and Molecular Biology for distinguished contributions to the field of Biochemistry and Molecular Biology and was awarded the Amersham Pharmacia Biotechnology Medal. He also received the David Syme Research Prize and Medal which is awarded for the best original research work in Biology, Chemistry, Geology or Physics, produced in Australia, during the preceding two years.
August 2002: To Junko Oshima, MD, PhD for her project entitled, "Cloning of the Gene for Hutchinson-Gilford Progeria Syndrome by Somatic Cell Complementation".
The goal of this research project is to identify the gene whose mutation is responsible for the Hutchinson-Gilford Progeria Syndrome (HGPS). Dr. Oshima and postdoctoral research associate Antonei Csoka have proposed to identify the HGPS gene by genetic studies of cells obtained from HGPS patients through the PRF Cell Bank. This project is a continuation of the PRF-funded project begun by John Sedivy at Brown University, who completed the first year of the two-year project in September.
Dr. Oshima is Research Associate Professor of Pathology at the University of Washington School of Medicine in Seattle, Washington. She is also a co-director of the International Registry of Werner Syndrome ("Progeria of Adults"), also located in Seattle. She is Director of the Genetics Approaches to Aging Training Program and Director of the University of Washington Nathan Shock Center for Excellence in the Basic Biology of Aging.
January 2001 (Start date July 2001): To John M. Sedivy, PhD
"Cloning the Gene for Hutchinson-Gilford Progeria Syndrome by Somatic Cell Complementation"
John M. Sedivy is a Professor of Biology and Medicine in the Department of Molecular Biology, Cell Biology and Biochemistry at Brown University. After completing his undergraduate studies at the University of Toronto in 1978, he obtained his PhD in 1984 in Microbiology and Molecular Genetics from Harvard University. After four years of postdoctoral training in somatic cell genetics in the laboratory of the Nobel laureate Philip Sharp at the Massachusetts Institute of Technology he started his independent research career in 1988 on the faculty of Yale University. He was named Presidential Young Investigator in 1990 and received the Andrew Mellon Award in 1991.
He moved to Brown University in 1996, where he teaches genetics and supervises a research group working on basic cancer biology and mechanisms of aging of human cells and tissues. He has served and continues to serve on numerous peer review committees for the National Institutes of Health and the American Cancer Society. His laboratory has been continuously funded by the National Institutes of Health, and has maintained a productive publication record in peer reviewed journals. In 2000 John Sedivy was named Director designate of the Center for Genetics and Genomics which is currently being established at Brown University.
The goal of the research project is to identify the gene whose mutation is responsible for the Hutchinson-Gilford Progeria Syndrome (HGPS). The gene for another progeroid syndrome, Werner's syndrome, has recently been identified through genetic studies of several large afflicted families. Unfortunately, this approach cannot be used in the case of HGPS because there are no families with extended HGPS pedigrees. Dr. Sedivy and his collaborator, Dr. Frank Rothman, have instead proposed to identify the HGPS gene by genetic studies of cells obtained from HGPS patients. This approach will take advantage of two recent developments in biotechnology: first, high density cDNA or oligonucleotide microarrays (commonly known as "Gene Chips"), which allow the study of numerous genes at one time; and second, retrovirus vector systems, which make it possible to engineer highly efficient transfer of genetic information from cell to cell. The researchers will first attempt to identify gene expression patterns that differentiate HGPS cells from normal cells, and then use the retrovirus vector technology to search for the gene (or genes) in normal cells that can "cure" the HGPS cells.
Frank G. Rothman, PhD, co-investigator
Frank G. Rothman is Professor of Biology and Provost, Emeritus at Brown University. He received his Ph.D. degree in chemistry from Harvard University in 1955. From 1957-1961, after two years of service in the U.S. Army, he was a postdoctoral research fellow and associate in molecular genetics at M.I.T. From 1961 until his retirement in 1997 he was on the Biology faculty of Brown University. He taught biochemistry, genetics, and molecular biology at all levels. His research on gene expression in microorganisms was continuously funded by the National Science Foundation from 1961 to 1984. He served as Dean of Biology from 1984-1990, and university Provost from 1990-1995. In the late 1980s he carried out research on aging in the roundworm, Caenorhabditis elegans. He taught courses in the Biology of Aging in 1988 and again in 1996. As Professor Emeritus, he has engaged in collaborative studies on the biology of aging, with a focus on Progeria."
December 2001: (Start date February 2002): To Thomas W. Glover, Ph.D.
"Genome Maintenance in Hutchinson-Gilford Progeria Syndrome"
Thomas W. Glover, Ph.D.: Dr. Glover is a Professor in the Departments of Human Genetics and Pediatrics at the University of Michigan, Ann Arbor, MI. His research focus is the molecular genetics of human genetic disorders and studies of chromosome instability and DNA repair. He has succeeded in identifying or cloning a number of human disease genes including those for Menkes syndrome, a common form of Ehlers-Danlos syndrome, and hereditary lymphedema. He has over 100 peer-reviewed scientific publications and has had continuous NIH grant support. He has served on several Editorial Boards and is a grant reviewer for the March of Dimes Birth Defects Foundation and the National Institutes of Health.
Michael W. Glynn, M.S. , co-investigator, is a senior graduate student pursuing a Ph.D. in Dr. Glover's laboratory in the Department of Human Genetics at the University of Michigan. He has completed qualifying for candidacy, and has finished all class work and teaching requirements. Honors include the James V. Neel Award for academic excellence awarded by the Department of Human Genetics. He is an author on several papers, a book chapter and two patents. Michael received a Masters of Science degree in Microbiology from the University of Connecticut. He went on to supervise the DNA Diagnostic Lab at Yale Medical School under the direction of Dr. Allen Bale.
The ultimate goal is to understand the basic defect responsible for HGPS. In this project, we will examine specific aspects of genome maintenance in HGPS cells. We will focus on three areas, telomere dynamics, spontaneous mutation rate, and specific.shtmlects of DNA repair. We will quantitatively measure rates of telomere degradation in HGPS fibroblasts by infecting cells with an hTERT (telomerase catalytic subunit) expressing retrovirus, modified to allow for strict control of telomerase expression. In addition, DNA maintenance will be examined to determine if HGPS, like many premature aging syndromes, involves a defect in DNA repair or replication. Studies will include examination of basal p53 levels in HGPS fibroblasts, the ability of HGPS fibroblasts to repair specific DNA lesions using lesion-specific antibodies, and examination of the rate of spontaneous mutations in HGPS fibroblasts. Many of the studies will include telomerase-immortalized fibroblast cell lines so that experiments can be performed without measuring effects caused by the premature senescence of HGPS fibroblasts. The proposed studies have the potential to give concrete answers as to whether the underlying defect in HGPS is due to faulty genome maintenance. Elucidation of cellular phenotypes associated with HGPS will be a valuable tool in determining the defective molecular pathways and, ultimately, in discovering the disease gene(s).
August 1999: To Leslie B. Gordon, MD, PhD
"The Pathophysiology of Arterioscleros is in Hutchinson-Gilford Progeria Syndrome"
January 2000: To Leslie B. Gordon, MD, PhD
"The Role of Hyaluronic Acid in Hutchinson-Gilford Progeria Syndrome"
Dr. Leslie Beth Gordon is an Instructor in Pediatrics at Hasbro Children's Hospital in Providence, Rhode Island and a Research Associate at Tufts University School of Medicine in Boston, Massachusetts, where she conducts her research on HGPS. She completed the combined MD, PhD program at Brown University School of Medicine in 1998, where she achieved the top-ranking category of outstanding in the medical program and became a member of the Sigma Xi Honor Society. . Prior to that, she received her Masters in Science from Brown University in 1991. Her Bachelor of Arts degree from the University of New Hampshire was awarded in 1986.
Dr. Gordon is focusing on the one consistent difference between Hutchinson-Gilford Progeria Syndrome (HGPS) patients and healthy children: the HGPS patients have much higher levels of a particular compound - hyaluronic acid (HA) - in their urine. HA is necessary for life because it helps hold tissue together, but too much of it might be a bad thing. HA concentrations creep up in elderly people, and plaques that build up in the blood vessels of people who die of heart disease are steeped in HA. The children with HGPS have these same plaques throughout their bodies, and that's what plays a major role in causing heart attacks and strokes. The idea that HA contributes to heart disease is not new, but work in this area has been fostered recently by new analytical tools. In this relatively unexplored area of research, Dr. Gordon is trying to follow the trickle of evidence to its source to find out whether the disease grows more severe as HA levels rise and to establish whether the chemical does indeed promote plaque formation. If such a connection were confirmed, it could lead to therapies that fight both Hutchinson-Gilford Progeria Syndrome and cardiovascular disease by lowering HA levels. "Any treatments that help these children will very likely help millions of people with cardiovascular disease and potentially other problems associated with aging", says Dr. Gordon.
Dr. Gordon is working in the laboratory of Dr. Bryan P. Toole, Professor of Anatomy at Tufts University School of Medicine. Others assisting in the project are Ingrid Harten M.S., Margaret Conrad, R.N., and Charlene Draleau, R.N