Pack S D, Bedanov V M, Sokolova O V, Zhdanova N S, Matveeva N M, Serov O L
Institute of Cytology and Genetics, Academy of Sciences of the USSR, Novosibirsk.
Mamm Genome. 1992;3(2):112-8. doi: 10.1007/BF00431255.
To expand the mink map, we established a new panel consisting of 23 mink-mouse clones. On the basis of statistical criteria (Wijnen et al. 1977; Burgerhout 1978), we developed a computer program for choice of clones of the panel. Assignments of the following mink genes were achieved with the use of the hybrid panel: glyoxalase (GLO), Chromosome (Chr) 1; acetyl acylase (ACY), Chr 5; creatine phosphokinase B (CKBB), Chr 10; alcohol dehydrogenase-2 (subunit B) (ADH2), Chr 8. Using a series of clones carrying rearrangements involving mink Chr 1 and 8, we assigned the gene for ME1 to the short arm of Chr 1 and that for ADH2 to Chr 8, in the region 8p12-p24. Mapping results confirm the ones we previously obtained with a mink-Chinese hamster panel. However, by means of an improved electrophoretic technique, we revised the localization of the gene for purine nucleoside phosphorylase (NP), which has been thought to be on mink Chr 2. It is reassigned to mink Chr 10.
为了扩展水貂基因图谱,我们建立了一个由23个水貂-小鼠克隆组成的新细胞系。基于统计学标准(Wijnen等人,1977年;Burgerhout,1978年),我们开发了一个用于选择该细胞系中克隆的计算机程序。利用这个杂交细胞系确定了以下水貂基因的位置:乙二醛酶(GLO),位于第1号染色体;乙酰基酰基酶(ACY),位于第5号染色体;肌酸磷酸激酶B(CKBB),位于第10号染色体;乙醇脱氢酶-2(亚基B)(ADH2),位于第8号染色体。通过使用一系列携带涉及水貂第1号和第8号染色体重排的克隆,我们将ME1基因定位于第1号染色体的短臂上,将ADH2基因定位于第8号染色体的8p12 - p24区域。图谱绘制结果证实了我们之前用水貂-中国仓鼠细胞系获得的结果。然而,通过改进的电泳技术,我们修正了嘌呤核苷磷酸化酶(NP)基因的定位,该基因之前被认为位于水貂第2号染色体上,现在重新定位于水貂第10号染色体上。