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由分配给大鼠第13号染色体的多态性DNA标记定义的9个基因座的连锁图谱。

Linkage map of nine loci defined by polymorphic DNA markers assigned to rat chromosome 13.

作者信息

Remmers E F, Goldmuntz E A, Zha H, Mathern P, Du Y, Crofford L J, Wilder R L

机构信息

Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Genomics. 1993 Nov;18(2):277-82. doi: 10.1006/geno.1993.1466.

Abstract

A genetic map of nine loci defined by polymorphic DNA markers was created using a single cross of F344/N and LEW/N rats. The markers contained polymorphic simple sequence repeats identified in five genes, renin (Ren), cardiac troponin T (Tnnt3), synaptotagmin (Syt2), Na+,K(+)-ATPase catalytic subunit (Atp1a2), and the Asp-, Gly-, Glu-, and Leu-tRNA gene cluster (Trnegl), as well as four anonymous DNA segments. Analysis of the segregation of the alleles of these markers in F2 intercross progeny of F344/N and LEW/N rats indicated the following locus order and distances between pairs of loci: D13N1-5 cM-Ren-1 cM-Tntt3-0 cM-Syt2-12 cM-D13N2-25 cM-Atp1a2-0 cM-Trnegl-7 cM-D13N3-4 cM-D13N4. Three of the loci, Ren, Trnegl, and Atp1a2, have previously been assigned to rat chromosome 13. Except for Ren, none of the loci have previously been mapped by linkage analysis. The markers for these loci were characterized in a total of 13 inbred rat strains (F344/N, LEW/N, LOU/MN, WBB1/N, WBB2/N, MR/N, MNR/N, ACI/N, SHR/N, WKY/N, BN/SsN, BUF/N, and LER/N) and were found to be highly polymorphic, with two to eight alleles detected for each marker. These markers expand the genetic map of the rat and should be valuable tools for future genetic studies. An examination of human and mouse comparative map information for all loci assigned to rat chromosome 13 shows significant synteny conservation with the q arm of human chromosome 1 and the distal portion of mouse chromosome 1.

摘要

利用F344/N和LEW/N大鼠的单杂交构建了由多态性DNA标记定义的9个基因座的遗传图谱。这些标记包含在5个基因中鉴定出的多态性简单序列重复,即肾素(Ren)、心肌肌钙蛋白T(Tnnt3)、突触结合蛋白(Syt2)、Na +,K(+)-ATP酶催化亚基(Atp1a2)以及天冬氨酸-、甘氨酸-、谷氨酸-和亮氨酸-tRNA基因簇(Trnegl),还有4个匿名DNA片段。对这些标记的等位基因在F344/N和LEW/N大鼠的F2互交后代中的分离分析表明了以下基因座顺序和基因座对之间的距离:D13N1 - 5厘摩 - Ren - 1厘摩 - Tntt3 - 0厘摩 - Syt2 - 12厘摩 - D13N2 - 25厘摩 - Atp1a2 - 0厘摩 - Trnegl - 7厘摩 - D13N3 - 4厘摩 - D13N4。其中3个基因座,Ren、Trnegl和Atp1a2,先前已被定位到大鼠第13号染色体上。除Ren外,这些基因座以前均未通过连锁分析进行定位。这些基因座的标记在总共13个近交大鼠品系(F344/N、LEW/N、LOU/MN、WBB1/N、WBB2/N、MR/N、MNR/N、ACI/N、SHR/N、WKY/N、BN/SsN、BUF/N和LER/N)中进行了特征分析,发现具有高度多态性,每个标记检测到2至8个等位基因。这些标记扩展了大鼠的遗传图谱,应为未来的遗传研究提供有价值的工具。对所有定位到大鼠第13号染色体的基因座的人类和小鼠比较图谱信息的检查显示,与人类第1号染色体的q臂和小鼠第1号染色体的远端部分存在显著的同线性保守性。

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