(Circulation. 1995;91:1311-1312.)
© 1995 American Heart Association, Inc.
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To guide its efforts in this emerging area, the Institute called upon an Expert Panel on Genetic Strategies for Heart, Lung, and Blood Diseases to formulate a Master Plan for the implementation of major research opportunities and strategies (see December 1993 Circulation). In this column, we highlight the development of two major initiatives recommended in the Master Plan: "Mammalian Genotyping Service" and "Genetic Map and Large Insert Library for the Rat Genome."
| Mammalian Genotyping Service |
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Competition for the NHLBI Mammalian Genotyping Service was announced in February 1994, and a contract was recently negotiated with the Center for Medical Genetics, Marshfield Medical Research Foundation. We believe that the existence of this facility will allow large populations and pedigrees to be analyzed reliably, with many genetic markers, at reduced cost. In addition, it is expected to significantly expedite current and future genetic studies of diseases whose pathogenesis involves more than one gene. As a final point, this service will provide greater access to cutting-edge technology.
As readers of Circulation may have observed, the Mammalian Genotyping Service has widely published a call for applications in relevant scientific journals. Genotyping with microsatellite DNA polymorphisms will begin in July 1995 at an initial minimal rate of 300 000 genotypes per year. For the first 2 years of operation, no fee will be charged for projects that fall within the domain of the NHLBI; beginning in 1997, a fee of approximately $1 per genotype will go into effect as the Service gradually becomes self-supporting. The facility will be monitored by an expert panel, which will also determine the priority of competing projects if demand exceeds capacity. Further information may be obtained from Beth Buescher, Center for Medical Genetics, Marshfield Medical Research Foundation, 1000 N Oak Ave, Marshfield, WI 54449 (phone, 715-389-3525; fax, 715-389-3808).
| Genetic Map and Large Insert Library for the Rat Genome |
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The rat is an important experimental model for studying human diseases such as hypertension, cancer, behavioral disorders, diabetes, drug abuse, alcoholism, and obesity. Because of its large size in comparison with the mouse, the rat is also widely used in studies of anatomy, pharmacology of the chemical senses, and neuronal pathways in the brain. The rat offers many advantages because a large body of knowledge about physiological mechanisms already exists, models that mimic human diseases are available, breeding is easy, and inbred congenic rat strains can be generated.
Nonetheless, research efforts to identify genetic factors involved in disease processes have been hampered in the rat by the lack of high-resolution genetic and physical maps of the rat genome. Currently, investigators using rats to map disease genes must resort to the laborious task of identifying new genetic markers and mapping large chromosomal regions of the genome before they can attempt to locate the gene of interest, thereby substantially slowing their progress.
The NIH currently supports projects aimed at mapping the human and mouse genomes as well as selected nonmammalian genomes. These efforts have led to substantial technological and methodological advances that are reducing the time and cost to construct genomic maps. However, because of a lack of sequence identity and specificity, only 5% to 10% of mouse and human genetic markers can be used to screen the rat genome. Therefore, these tools must be generated specifically for the rat if we wish efforts to map disease genes in rat models to be continued.
This new program can be expected to expedite the timely and cost-effective development of critical mapping resources necessary to develop the full potential of the rat as an experimental model. Because rats are used extensively to study normal and disease processes, we believe that the program will provide a valuable resource that spans the diverse interests of the research community.
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