Cash J M, Remmers E F, Goldmuntz E A, Crofford L J, Zha H, Hansen C T, Wilder R L
Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892.
Mamm Genome. 1993;4(1):37-42. doi: 10.1007/BF00364661.
The nude trait in the rat is transmitted in an autosomal recessive manner and is associated with thymic aplasia, T-cell deficiency, and hairlessness. Congenic rats homozygous for the RNU (Rowett nude) locus are important models in the study of inflammatory disease, tumor growth, and transplant rejection. The RNU locus has not been previously mapped, and the nature of the gene product is unknown. To determine the map location of this gene, a single F344.rnu/rnu (athymic nude congenic Fischer rat) male congenic rat was bred with 3 LEW/N (NIH stock Lewis rat) female rats to produce F1 progeny. Twelve F1 brother-sister breeding pairs were established. Forty-nine phenotypically nude F2 offspring (198 total) were obtained. Linkage analysis done on F2 DNA revealed highly significant cosegregation between the nude phenotype and eight polymorphic markers located on Chromosome (Chr) 10. The tightest linkages were with: MYH3 (embryonic, skeletal myosin heavy chain) and SHBG (sex hormone-binding globulin), giving 2 point lod scores of 20.2, and 20.0, respectively. The map order and map distances, determined by multipoint linkage calculations, were: RR24-(16.1 cM)-MYH3-(3.5 cM)-SHBG-(4.7 cM)-RNU-(11.9 cM)-F16F2-(24.1 cM)-CLATP (citrate lyase ATPase)-(2.4 cM)-ACE (angiotensin converting enzyme)/PPY (pancreatic polypeptide)-(14.1 cM)-RR1023. The position of the RNU locus in the rat corresponds closely with that of the recently reported nu locus in the mouse. This finding suggests that the nude phenotype in the rat and the mouse arise from defects in homologous genes.
大鼠的裸鼠性状以常染色体隐性方式遗传,与胸腺发育不全、T细胞缺陷和无毛有关。RNU(罗威特裸鼠)位点纯合的近交系大鼠是研究炎症性疾病、肿瘤生长和移植排斥的重要模型。RNU位点以前尚未定位,基因产物的性质也未知。为了确定该基因的图谱位置,将一只F344.rnu/rnu(无胸腺裸鼠近交系费希尔大鼠)雄性近交系大鼠与3只LEW/N(美国国立卫生研究院品系刘易斯大鼠)雌性大鼠交配,以产生F1代后代。建立了12对F1代兄妹繁殖对。获得了49只表型为裸鼠的F2代后代(共198只)。对F2代DNA进行的连锁分析显示,裸鼠表型与位于第10号染色体(Chr)上的8个多态性标记之间存在高度显著的共分离。最紧密的连锁是与:MYH3(胚胎型、骨骼肌肌球蛋白重链)和SHBG(性激素结合球蛋白),两点连锁值分别为20.2和20.0。通过多点连锁计算确定的图谱顺序和图谱距离为:RR24 -(16.1厘摩)- MYH3 -(3.5厘摩)- SHBG -(4.7厘摩)- RNU -(11.9厘摩)- F16F2 -(24.1厘摩)- CLATP(柠檬酸裂解酶ATP酶)-(2.4厘摩)- ACE(血管紧张素转换酶)/PPY(胰多肽)-(14.1厘摩)- RR1023。大鼠中RNU位点的位置与最近报道的小鼠nu位点的位置密切对应。这一发现表明,大鼠和小鼠的裸鼠表型源于同源基因的缺陷。