Dracheva S V, Remmers E F, Chen S, Chang L, Gulko P S, Kawahito Y, Longman R E, Wang J, Du Y, Shepard J, Ge L, Joe B, Kotake S, Salstrom J L, Furuya T, Hoffman J, Cannon G W, Griffiths M M, Wilder R L
The Inflammatory Joint Diseases Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland 20892, USA.
Genomics. 2000 Jan 15;63(2):202-26. doi: 10.1006/geno.1999.6074.
The rat (Rattus norvegicus) is an important experimental model for many human diseases including arthritis, diabetes, and other autoimmune and chronic inflammatory diseases. The rat genetic linkage map, however, is less well developed than those of mouse and human. Integrated rat genetic linkage maps have been previously reported by Pravenec et al. (1996, Mamm. Genome 7: 117-127) (500 markers mapped in one cross), Bihoreau et al. (1997, Genome Res. 7: 434-440) (767 markers mapped in three crosses), Wei et al. (1998, Mamm. Genome 9: 1002-1007) (562 markers mapped in two crosses), Brown et al. (1998, Mamm. Genome 9: 521-530) (678 markers mapped in four crosses), and Nordquist et al. (1999, Rat Genome 5: 15-20) (330 markers mapped in two crosses). The densest linkage map combined with a radiation hybrid map, reported by Steen et al. (1999, Genome Res. 9: AP1-AP8), includes 4736 markers mapped in two crosses. Here, we present an integrated linkage map with 1137 markers. We have constructed this map by genotyping F2 progeny of five crosses: F344/NHsd x LEW/NHsd (673 markers), DA/Bkl x F344/NHsd (531 markers), BN/SsN x LEW/N (714 markers), DA/Bkl x BN/SsNHsd (194 markers), and DA/Bkl x ACI/SegHsd (245 markers). These inbred rat strains vary in susceptibility/resistance to multiple autoimmune diseases and are used extensively for many types of investigation. The integrated map includes 360 loci mapped in three or more crosses. The map contains 196 new SSLP markers developed by our group, as well as many SSLP markers developed by other groups. Two hundred forty genes are incorporated in the map. This integrated map should allow comparison of rat genetic maps from different groups and thereby facilitate genetic studies of rat autoimmune and related disease models.
大鼠(褐家鼠)是许多人类疾病的重要实验模型,包括关节炎、糖尿病以及其他自身免疫性和慢性炎症性疾病。然而,大鼠的遗传连锁图谱不如小鼠和人类的完善。Pravenec等人(1996年,《哺乳动物基因组》7: 117 - 127)(在一次杂交中定位了500个标记)、Bihoreau等人(1997年,《基因组研究》7: 434 - 440)(在三次杂交中定位了767个标记)、Wei等人(1998年,《哺乳动物基因组》9: 1002 - 1007)(在两次杂交中定位了562个标记)、Brown等人(1998年,《哺乳动物基因组》9: 521 - 530)(在四次杂交中定位了678个标记)以及Nordquist等人(1999年,《大鼠基因组》5: 15 - 20)(在两次杂交中定位了330个标记)此前都报道过整合的大鼠遗传连锁图谱。Steen等人(1999年,《基因组研究》9: AP1 - AP8)报道的结合了辐射杂种图谱的最密集连锁图谱,在两次杂交中定位了4736个标记。在此,我们展示一个包含1137个标记的整合连锁图谱。我们通过对五个杂交组合的F2后代进行基因分型构建了该图谱:F344/NHsd×LEW/NHsd(673个标记)、DA/Bkl×F344/NHsd(531个标记)、BN/SsN×LEW/N(714个标记)、DA/Bkl×BN/SsNHsd(194个标记)以及DA/Bkl×ACI/SegHsd(245个标记)。这些近交大鼠品系对多种自身免疫性疾病的易感性/抗性各不相同,并且被广泛用于多种类型的研究。该整合图谱包括在三次或更多次杂交中定位的360个基因座。该图谱包含我们小组开发的196个新的简单序列长度多态性(SSLP)标记,以及其他小组开发的许多SSLP标记。图谱纳入了240个基因。这个整合图谱应该能够比较不同小组的大鼠遗传图谱,从而促进对大鼠自身免疫及相关疾病模型的遗传学研究。