Linkage disequilibrium between two genetic loci of the major histocompatibility complex in rats |
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Authors: | Dr. Diane K. Wagener Donald V. Cramer John W. Shonnard Bridgett K. Davis |
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Affiliation: | (1) Departments of Psychiatry and Biostatistics, University of Pittsburgh, USA;(2) Departments of Pathology, School of Medicine, University of Pittsburgh, USA;(3) Veterans' Administration Hospital, Pittsburgh, PA;(4) Department of Psychiatry, University of Pittsburgh School of Medicine, 3811 O'Hara Street, 15261 Pittsburgh, Pennsylvania |
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Abstract: | The major histocompatibility complex (MHC) in natural populations of rats is composed of genetic phenotypes that are similar, if not identical, to those seen in inbred laboratory strains. Examination of individual wild rats from a single location in the city of Pittsburgh, Pennsylvania, resulted in the identification of seven different RT1.A histocompatibility serotypes and three RT1.B mixed lymphocytes responses. In this population of animals there is a significant association (p < 0.005) between four RT1.A and RT1.B phenotypic pairs: RT1.A8B1, RTl.AkBn, RTl.AdBa and RT1.A1Ba. The observed values for linkage disequilibrium (0.211,0.076,0.070 and 0.085, respectively) are very high and are close to the maximum expected, given the individual allelic frequencies. Although the animals included in this study were obtained from one location, agreement with Hardy-Weinberg equilibrium is demonstrated for other loci in the same population. The demonstration of equilibrium suggests that significant inbreeding is not affecting this population of rats. Not enough is known about the allelic frequencies in surrounding rat populations to determine how important the effect of migration is on these disequilibrium values. The large linkage disequilibria may indicate that, in the rat, environmental selective forces are operating to ensure the nonrandom association of separate components of the MHC. |
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