Maureen Hanson | |
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Alma mater | Duke University (B.S) Harvard University (Ph.D) |
Awards | Lawrence Bogorad Award of the American Society of Plant Biologists (2006) Cornell University Award for Outstanding Accomplishments in Basic Research (2009) |
Scientific career | |
Fields | Plant reproductive biology Plant organelle biology |
Institutions | University of Virginia Cornell University |
Thesis | The genetics and biochemistry of chloroplast ribosomes mutants of Chlamydomonas reinhardi (1976) |
Website | https://hansonlab.org/ https://neuroimmune.cornell.edu/ |
Maureen Hanson is an American molecular biologist and Liberty Hyde Bailey Professor in the Department of Molecular Biology and Genetics at Cornell University in Ithaca, New York. [1] She is a joint member of the Section of Plant Biology and Director of the Center for Enervating Neuroimmune Disease. Her research concerns gene expression in chloroplasts and mitochondria, photosynthesis, and the molecular basis of the disease Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).
Hanson grew up in the Maryland suburbs of Washington D.C. She attended Duke University, where she received a B.S. degree in Botany. She completed a Ph.D. in Lawrence Bogorad's lab in the Department of Biology at Harvard University. [2] Subsequently, she held an National Institutes of Health National Research Service Award postdoctoral fellowship in Frederick M. Ausubel’s lab at Harvard.
Hanson joined the faculty of the Department of Biology at the University of Virginia, Charlottesville, as Assistant Professor in 1979. There she studied the phenomenon of cytoplasmic male sterility (CMS), using the model system Petunia. With Ellora Young, she identified a mutant chimeric mitochondrial gene that encodes a toxic protein that results in abortion of pollen development. [3] Subsequently, most CMS-encoding genes have been found to be composed of abnormal chimeric gene fusions. [4] After she moved to Cornell in 1985 as Associate Professor, Stéphane Bentolila in her group used map-based cloning to find the dominant nuclear Restorer of Fertility (Rf) gene, [5] making Petunia the first plant to have both the CMS mitochondrial gene and nuclear restorer pair identified in the same species. The Petunia Rf gene was the first such gene to be identified as encoding a pentatricopeptide repeat (PPR) protein, part of a family now known to also be involved in organelle RNA editing and other types of RNA metabolism. Most of the Rf genes cloned from other species have been found to be PPR proteins.
Hanson’s group was the first to utilize GFP technology to label plastids and mitochondria in plants. As a result, Rainer Köhler in her group rediscovered plastid protrusions, [6] which had been observed as long ago as 1908, but not previously established as a genuine feature of plant cell biology. Hanson named these structures “stromules” and demonstrated that proteins flow through them and examined their tissue-specific abundance. [7] [8] Now it is known that these structures are involved in a number of phenomena, include plant defense responses. [9]
Hanson has also made many contributions to the understanding of C-to-U RNA editing in chloroplasts and plant mitochondria. [10] [11] Among these are the identification of several of the protein families whose members form the diverse set of editosomes, RNA/protein complexes that carry out editing in plant organelles. [12] [13] [14]
Hanson began working in the area of synthetic biology for improving photosynthesis in 2011. Since then, her lab has published on attempts to introduce cyanobacterial carboxysomes into plants and engineering Rubisco, with collaborating labs of Martin Parry (Lancaster, UK) and Stephen Long (U. Illinois). [15] [16] Her lab utilizes chloroplast transformation to modify plants. [17]
Due to personal interest in the disease, in 2009 Hanson initiated an additional research program on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). Her group has increased the understanding of the disruptions at the molecular level that occur in this disease, which was long erroneously claimed to be a psychological illness. Her lab has demonstrated an altered gut microbiome [18] [19] and altered plasma metabolites, [20] [21] characterized mitochondrial genomes [22] and extracellular vesicles, observed abnormal cytokine networks, [23] and examined T cell metabolism in ME/CFS patients vs. controls [24]
A chloroplast is a type of membrane-bound organelle known as a plastid that conducts photosynthesis mostly in plant and algal cells. The photosynthetic pigment chlorophyll captures the energy from sunlight, converts it, and stores it in the energy-storage molecules ATP and NADPH while freeing oxygen from water in the cells. The ATP and NADPH is then used to make organic molecules from carbon dioxide in a process known as the Calvin cycle. Chloroplasts carry out a number of other functions, including fatty acid synthesis, amino acid synthesis, and the immune response in plants. The number of chloroplasts per cell varies from one, in unicellular algae, up to 100 in plants like Arabidopsis and wheat.
Symbiogenesis is the leading evolutionary theory of the origin of eukaryotic cells from prokaryotic organisms. The theory holds that mitochondria, plastids such as chloroplasts, and possibly other organelles of eukaryotic cells are descended from formerly free-living prokaryotes taken one inside the other in endosymbiosis. Mitochondria appear to be phylogenetically related to Rickettsiales bacteria, while chloroplasts are thought to be related to cyanobacteria.
The plastid is a membrane-bound organelle found in the cells of plants, algae, and some other eukaryotic organisms. They are considered to be intracellular endosymbiotic cyanobacteria. Examples include chloroplasts, chromoplasts, and leucoplasts.
Coxsackie B is a group of six serotypes of coxsackievirus (CVB1-CVB6), a pathogenic enterovirus, that trigger illness ranging from gastrointestinal distress to full-fledged pericarditis and myocarditis.
Enterovirus is a genus of positive-sense single-stranded RNA viruses associated with several human and mammalian diseases. Enteroviruses are named by their transmission-route through the intestine.
A nuclear gene is a gene that has its DNA nucleotide sequence physically situated within the cell nucleus of a eukaryotic organism. This term is employed to differentiate nuclear genes, which are located in the cell nucleus, from genes that are found in mitochondria or chloroplasts. The vast majority of genes in eukaryotes are nuclear.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) has a long history with an evolution in medical understanding, diagnoses and social perceptions.
Treatment of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is variable and uncertain, and the condition is primarily managed rather than cured.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is an illness with a long history of controversy. Some professionals within the medical community do not recognize ME/CFS as a genuine condition, nor is there agreement on its prevalence. There has been much disagreement over the pathophysiology of chronic fatigue syndrome, how it should be diagnosed, and how to treat it.
Clinical descriptions of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) vary. Different groups have produced sets of diagnostic criteria that share many similarities. The biggest differences between criteria are whether post-exertional malaise (PEM) is required, and the number of symptoms needed. The pathology of ME/CFS is unknown, and it can be a difficult condition to diagnose because there is no standard test, many symptoms are non-specific, and because doctors and patients may be unfamiliar with post-exertional malaise. Subgroup analysis suggests that, depending on the applied definition, CFS may represent a variety of conditions rather than a single disease entity.
Graded exercise therapy (GET) is a programme of physical activity that starts very slowly and gradually increases over time, intended as a treatment for chronic fatigue syndrome. Most public health bodies, including the CDC and NICE, consider it ineffective, and its safety is disputed. However, GET still enjoys support among a minority of clinicians and organizations.
Chloroplast DNA (cpDNA) is the DNA located in chloroplasts, which are photosynthetic organelles located within the cells of some eukaryotic organisms. Chloroplasts, like other types of plastid, contain a genome separate from that in the cell nucleus. The existence of chloroplast DNA was identified biochemically in 1959, and confirmed by electron microscopy in 1962. The discoveries that the chloroplast contains ribosomes and performs protein synthesis revealed that the chloroplast is genetically semi-autonomous. The first complete chloroplast genome sequences were published in 1986, Nicotiana tabacum (tobacco) by Sugiura and colleagues and Marchantia polymorpha (liverwort) by Ozeki et al. Since then, a great number of chloroplast DNAs from various species have been sequenced.
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating long-term medical condition. People with ME/CFS experience lengthy flare-ups of the illness following relatively minor physical or mental activity. This is known as post-exertional malaise (PEM) and is the hallmark symptom of the illness. Other core symptoms are a greatly reduced ability to do tasks that were previously routine, severe fatigue, and sleep disturbances. The baseline fatigue in ME/CFS does not improve much with rest. Orthostatic intolerance, memory and concentration problems, and chronic pain are common. About a quarter of people with ME/CFS are severely affected and unable to leave their bed or home.
Jennifer Brea is an American documentary filmmaker and activist. Her debut feature, Unrest, premiered at the 2017 Sundance Film Festival and received the US Documentary Special Jury Award For Editing. Brea also co-created a virtual reality film which premiered at Tribeca Film Festival.
Post-exertional malaise (PEM), sometimes referred to as post-exertional symptom exacerbation (PESE), is a worsening of symptoms that occurs after minimal exertion. It is the hallmark symptom of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and common in long COVID. PEM is often severe enough to be disabling, and is triggered by ordinary activities that healthy people tolerate. Typically, it begins 12–48 hours after the activity that triggers it, and lasts for days, but this is highly variable and may persist much longer. Management of PEM is symptom-based, and patients are recommended to pace their activities to avoid triggering PEM.
A plastid is a membrane-bound organelle found in plants, algae and other eukaryotic organisms that contribute to the production of pigment molecules. Most plastids are photosynthetic, thus leading to color production and energy storage or production. There are many types of plastids in plants alone, but all plastids can be separated based on the number of times they have undergone endosymbiotic events. Currently there are three types of plastids; primary, secondary and tertiary. Endosymbiosis is reputed to have led to the evolution of eukaryotic organisms today, although the timeline is highly debated.
Peter C. Rowe is a physician and academic. A leading researcher in chronic fatigue syndrome, he is Professor of Pediatrics, Sunshine Natural Wellbeing Foundation Professor of Chronic Fatigue and Related Disorders, and Director of the Children's Center Chronic Fatigue Clinic at Johns Hopkins University School of Medicine.
A 2-day CPET is a cardiopulmonary exercise test given on two successive days to measure the effect of post-exertional malaise (PEM) on a patient's ability to exercise. PEM is a cardinal symptom of myalgic encephalomyelitis/chronic fatigue syndrome and is common in long COVID as well.
Andrew Melvin Ramsay (1901–1990) was a British physician, who is known for his research and advocacy on myalgic encephalomyelitis (ME), a chronic disease causing muscle weakness and cognitive dysfunction. Ramsay worked as a consultant at the Royal Free Hospital in London during a mysterious 1955 disease outbreak of what later became known as ME. He studied the disease and similar outbreaks elsewhere. Work by Ramsay showed that although ME seldom caused death, the disease could be highly disabling.
Carmen Scheibenbogen is a German professor, doctor and acting director of the Institute for Medical Immunology of the Charité university hospital in Berlin. She specialises in hematology, oncology and immunology. She leads the Outpatient Clinic for Immunodeficiency and the Fatigue Centre at the Charité hospital. She is one of the few doctors specialised in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) in Germany, and also researches Long COVID.