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Guide for the Care and Use of Laboratory Animals - Office of ...

Guide for the Care and Use of Laboratory Animals - Office of ...

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6GUIdE FOR ThE CARE ANd USE OF LAbORATORy ANIMALSdate <strong>of</strong> inoculations, history <strong>of</strong> surgical procedures <strong>and</strong> postoperative care,in<strong>for</strong>mation on experimental use, <strong>and</strong> necropsy findings where applicable.Basic demographic in<strong>for</strong>mation <strong>and</strong> clinical histories enhance <strong>the</strong> value<strong>of</strong> individual animals <strong>for</strong> both breeding <strong>and</strong> research <strong>and</strong> should be readilyaccessible to investigators, veterinary staff, <strong>and</strong> animal care staff.breeding, Genetics, <strong>and</strong> Nomenclature Genetic characteristics are importantwith regard to <strong>the</strong> selection <strong>and</strong> management <strong>of</strong> animals <strong>for</strong> use inbreeding colonies <strong>and</strong> in biomedical research (see Appendix A). Pedigreein<strong>for</strong>mation allows appropriate selection <strong>of</strong> breeding pairs <strong>and</strong> <strong>of</strong> experimentalanimals that are unrelated or <strong>of</strong> known relatedness.Outbred animals are widely used in biomedical research. Foundingpopulations should be large enough to ensure <strong>the</strong> long-term genetic heterogeneity<strong>of</strong> breeding colonies. To facilitate direct comparison <strong>of</strong> researchdata derived from outbred animals, genetic management techniques shouldbe used to maintain genetic variability <strong>and</strong> equalize founder representations(Hartl 2000; Lacy 1989; Poiley 1960; Williams-Blangero 1991). Geneticvariability can be monitored with computer simulations, biochemical markers,DNA markers <strong>and</strong> sequencing, immunologic markers, or quantitativegenetic analyses <strong>of</strong> physiologic variables (MacCluer et al. 1986; Williams-Blangero 1993).Inbred strains <strong>of</strong> various species, especially rodents, have been developedto address specific research needs (Festing 1979; Gill 1980). Wheninbred animals or <strong>the</strong>ir F1 progeny are used, it is important to periodicallymonitor genetic au<strong>the</strong>nticity (Festing 1982; Hedrich 1990); several methods<strong>of</strong> monitoring have been developed that use immunologic, biochemical,<strong>and</strong> molecular techniques (Cramer 1983; Festing 2002; Groen 1977; H<strong>of</strong>fmanet al. 1980; Russell et al. 1993). Appropriate management systems(Green 1981; Kempthorne 1957) should be designed to minimize geneticcontamination resulting from mutation <strong>and</strong> mismating.Genetically modified animals (GMAs) represent an increasingly largeproportion <strong>of</strong> animals used in research <strong>and</strong> require special considerationin <strong>the</strong>ir population management. Integrated or altered genes can interactwith species or strain-specific genes, o<strong>the</strong>r genetic manipulations, <strong>and</strong>environmental factors, in part as a function <strong>of</strong> site <strong>of</strong> integration, so eachGMA line can be considered a unique resource. <strong>Care</strong> should be taken topreserve such resources through st<strong>and</strong>ard genetic management procedures,including maintenance <strong>of</strong> detailed pedigree records <strong>and</strong> genetic monitoringto verify <strong>the</strong> presence <strong>and</strong> zygosity <strong>of</strong> transgenes <strong>and</strong> o<strong>the</strong>r geneticmodifications (Conner 2005). Cryopreservation <strong>of</strong> fertilized embryos, ova,ovaries, or spermatozoa should also be considered as a safeguard againstalterations in transgenes over time or accidental loss <strong>of</strong> GMA lines (Conner2002; Liu et al. 2009).

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