This article contains content that is written like an advertisement .(October 2020) |
Established | May 4, 1929 |
---|---|
Founder | C. C. Little |
Type | Nonprofit organization Research institute |
Headquarters | Bar Harbor, Maine, U.S. |
Location | |
Locations | |
Products | Mice, C57BL/6J Model Organisms Laboratory Animals |
Fields | |
Leader | Lon Cardon |
Budget (2023) | $628M [1] |
Staff | 3,000 |
Website | jax |
The Jackson Laboratory (often abbreviated as JAX) is an independent, non-profit biomedical research institution which was founded by Clarence Cook Little in 1929. [2] It employs over 3,000 employees in Bar Harbor, Maine; Sacramento, California; Farmington, Connecticut; Shanghai, China; and Yokohama, Japan. [3] The institution is a National Cancer Institute-designated Cancer Center [4] and has NIH Centers of Excellence in aging [5] and systems genetics. [1] The stated mission of The Jackson Laboratory is "to discover the genetic basis for preventing, treating and curing human diseases, and to enable research and education for the global biomedical community." [6]
The laboratory also provides more than 13,000 strains of mouse models to more than 2,400 organizations in 68 countries around the world. [1] Additionally, JAX is the home of the Mouse Genome Informatics database, and an international hub for scientific courses, conferences, training and education. [7]
The Jackson Laboratory has two research campuses, the Jackson Laboratory for Mammalian Genetics located in Bar Harbor, Maine, and the Jackson Laboratory for Genomic Medicine located in Farmington, Connecticut. [8] Each campus maintains affiliations with a variety of other academic institutions. In the Bar Harbor location, cooperative Ph.D. training is offered in conjunction with the University of Maine [9] and Tufts University. [10] [11] At the Jackson Laboratory for Genomic Medicine, cooperative Ph.D. training is offered in conjunction with the University of Connecticut Health Center. There are more than 60 faculty members maintaining independent labs across these campuses, who perform research in six primary areas: [12]
The Jackson Laboratory was founded by Clarence Cook Little, a former University of Maine and University of Michigan president, in 1929 in Bar Harbor, Maine under the name Roscoe B. Jackson Memorial Laboratory with the purpose of discovering the causes of cancer and other diseases through research on mammals. [13] [14] The campus was built on 13 acres of land donated by George Dorr. Initial funding for the laboratory campus came from Edsel Ford, the son of Henry Ford, and from Roscoe B. Jackson, a one-time head of the Hudson Motor Car Company, for whom the institution is named. [13] [15] As well as providing funds for the first laboratory building, Roscoe B. Jackson provided support for the first five years of operation. [15]
The sale of mouse animal models began in 1933 with early sales to the United States Public Health Service and The Jackson Laboratory now provides a high proportion of the mice used in biomedical research [16] In particular, the C57BL/6J strain, which is widely used and cited is maintained at The Jackson Laboratory. [16] [17] The demand for mice generated at The Jackson Lab increased in 1937 when the Surgeon General supported a grant from National Cancer Institute to the lab that made mice produced there a de facto industry standard due to federal standardization requirements because it was the only large-scale mouse provider before World War II. [17]
The research performed at The Jackson Laboratory is associated with at least 26 Nobel Prizes in Physiology or Medicine via research, resources, or educational programming. Some notable findings from the institution include:
The Jackson Laboratory Cancer Center (JAXCC) first received its National Cancer Institute designation in 1983 in recognition of the foundational cancer research conducted there. The JAXCC is one of seven NCI-designated Cancer Centers with a focus on basic research. [25]
The Jackson Laboratory Cancer Center has a single program, Genetic Models for Precision Cancer Medicine, composed of three biological themes: cancer cell robustness, genomic and genetic complexity, and progenitor cell biology. The themes emphasize the systems genetics of cancer and translational cancer genomics, and all are supported by the JAX Cancer Center's technological initiatives in mouse modeling, genome analytics and quantitative cell biology. [25]
On May 10, 1989, a flash fire destroyed the Morrell Park mouse production facility. [26] The fire lasted for five hours, requiring over 100 firefighters from 15 companies and a total of 16 trucks for the fire to be contained. Four workers of the Colwell Construction Company who were installing fiberglass wallboard in the room where the fire broke out were injured, one with burns over 15 percent of his body. While none of the foundation strains were lost, 300,000 production mice (about 50% of their stock) died, resulting in a national shortage of laboratory mice and the layoff of 60 employees. [27]
This was the second fire to severely affect the laboratory; the 1947 fire that burned most of the island destroyed most of the laboratory, and its mice. Worldwide donations of funds and mice allowed the lab to resume operations in 1948. [28]
In October 2021, Jackson Lab bought Japan-based research animal business from Charles River Laboratories International for US$63 million. [29]
The Jackson Laboratory is recognized by the IRS as a public charity. [31] According to organization literature, revenue comes primarily from the sale of materials and services (~70%) and from government support (~25%). [32] Less than 5% of 2012 revenue came from charitable donations. [32]
In 2013, a jury in Maine found that Jackson Laboratory did not violate that state's whistleblower protection law when they fired an employee who claimed to have been terminated after reporting her concerns about the treatment of animals to the National Institutes of Health Office for Laboratory Animal Welfare. The worker accused the laboratory of "allowing mice to suffer and then die in their cages instead of euthanizing them" and of cutting off the toes of mice to identify them. Jackson Laboratory denied the allegations and stated the worker was fired for her confrontational demeanor. [33]
In 2009, Jackson Laboratory was fined $161,680 by the EPA for improperly handling and storing hazardous materials. [34]
A model organism is a non-human species that is extensively studied to understand particular biological phenomena, with the expectation that discoveries made in the model organism will provide insight into the workings of other organisms. Model organisms are widely used to research human disease when human experimentation would be unfeasible or unethical. This strategy is made possible by the common descent of all living organisms, and the conservation of metabolic and developmental pathways and genetic material over the course of evolution.
Cold Spring Harbor Laboratory (CSHL) is a private, non-profit institution with research programs focusing on cancer, neuroscience, plant biology, genomics, and quantitative biology. It is located in Laurel Hollow on Long Island, New York.
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The history of model organisms began with the idea that certain organisms can be studied and used to gain knowledge of other organisms or as a control (ideal) for other organisms of the same species. Model organisms offer standards that serve as the authorized basis for comparison of other organisms. Model organisms are made standard by limiting genetic variance, creating, hopefully, this broad applicability to other organisms.
The Cancer Genome Project is part of the cancer, aging, and somatic mutation research based at the Wellcome Trust Sanger Institute in the United Kingdom. It aims to identify sequence variants/mutations critical in the development of human cancers. Like The Cancer Genome Atlas project within the United States, the Cancer Genome Project represents an effort in the War on Cancer to improve cancer diagnosis, treatment, and prevention through a better understanding of the molecular basis of the disease. The Cancer Genome Project was launched by Michael Stratton in 2000, and Peter Campbell is now the group leader of the project. The project works to combine knowledge of the human genome sequence with high throughput mutation detection techniques.
Mouse Genome Informatics (MGI) is a free, online database and bioinformatics resource hosted by The Jackson Laboratory, with funding by the National Human Genome Research Institute (NHGRI), the National Cancer Institute (NCI), and the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). MGI provides access to data on the genetics, genomics and biology of the laboratory mouse to facilitate the study of human health and disease. The database integrates multiple projects, with the two largest contributions coming from the Mouse Genome Database and Mouse Gene Expression Database (GXD). As of 2018, MGI contains data curated from over 230,000 publications.
Conditional gene knockout is a technique used to eliminate a specific gene in a certain tissue, such as the liver. This technique is useful to study the role of individual genes in living organisms. It differs from traditional gene knockout because it targets specific genes at specific times rather than being deleted from beginning of life. Using the conditional gene knockout technique eliminates many of the side effects from traditional gene knockout. In traditional gene knockout, embryonic death from a gene mutation can occur, and this prevents scientists from studying the gene in adults. Some tissues cannot be studied properly in isolation, so the gene must be inactive in a certain tissue while remaining active in others. With this technology, scientists are able to knockout genes at a specific stage in development and study how the knockout of a gene in one tissue affects the same gene in other tissues.
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A genetically modified mouse or genetically engineered mouse model (GEMM) is a mouse that has had its genome altered through the use of genetic engineering techniques. Genetically modified mice are commonly used for research or as animal models of human diseases and are also used for research on genes. Together with patient-derived xenografts (PDXs), GEMMs are the most common in vivo models in cancer research. Both approaches are considered complementary and may be used to recapitulate different aspects of disease. GEMMs are also of great interest for drug development, as they facilitate target validation and the study of response, resistance, toxicity and pharmacodynamics.
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