Masuyama T, Ishibiki J, Awata T, Noda M, Kanazawa Y, Sugawara M, Komeda K
Research Laboratories, Torii Pharmaceutical Co Ltd, Chiba, Japan.
Comp Med. 2000 Aug;50(4):369-73.
Rat chromosome 20 is one of special interest because it contains some diabetogenic genes, such as a major histocompatibilitiy complex (MHC)-linked genetic components and quantitative trait loci. We studied rat chromosome 20, using the backcross progeny between BB/Wor and PVG.R23 rats, and confirmed the genetic linkage map by use of another backcross panel.
Backcross panels were done between BB/Wor and PVG.R23 rats, and BN and KZC rats. Length variations of simple sequence length polymorphism markers were analyzed by use of polymerase chain reaction (PCR) analysis. Alleles of RT1-Bb and RT1-Db were analyzed by use of the PCR-restriction fragment length polymorphism method. Genetic maps of rat chromosome 20 were constructed, using the Map Manager computer program.
Fifty-two loci were mapped on rat chromosome 20. Genetic length was 57.9 cM, with average spanning of 1.11 cM between markers. The positions of RT1-N1, Tnf, and RT1-Bb into the MHC region were separated and confirmed by results of two backcross panels in our linkage studies.
The genetic linkage map of rat chromosome 20 was improved, and was a useful tool for genetic analysis of a diabetogenic gene(s) and for producing MHC congenic strains.
大鼠20号染色体备受关注,因为它包含一些致糖尿病基因,如主要组织相容性复合体(MHC)相关的遗传成分和数量性状基因座。我们利用BB/Wor和PVG.R23大鼠之间的回交后代研究了大鼠20号染色体,并通过另一个回交群体证实了遗传连锁图谱。
进行了BB/Wor与PVG.R23大鼠以及BN与KZC大鼠之间的回交。利用聚合酶链反应(PCR)分析简单序列长度多态性标记的长度变异。采用PCR-限制性片段长度多态性方法分析RT1-Bb和RT1-Db的等位基因。使用Map Manager计算机程序构建大鼠20号染色体的遗传图谱。
52个基因座被定位到大鼠20号染色体上。遗传长度为57.9厘摩,标记间平均跨度为1.11厘摩。在我们的连锁研究中,通过两个回交群体的结果,RT1-N1、Tnf和RT1-Bb在MHC区域的位置被分离并得到证实。
大鼠20号染色体的遗传连锁图谱得到了改进,是分析致糖尿病基因和培育MHC同源品系的有用工具。