Koizumi T
Experimental Animal Center, Fukui Medical School, Japan.
Exp Anim. 1995 Oct;44(4):323-7. doi: 10.1538/expanim.44.323.
A survey of inbred strains of mice revealed genetic variation in DNase II activity in the spleen, liver, kidney, lung, heart, coagulating gland and preputial gland. Since DNase II activities in these tissues were closely correlated to each other, systemic regulation of the enzyme was suggested. The inheritance of quantitative variation in the DNase II activity was studied in a test cross using the spleen DNase II activity level as an indicator of progeny phenotypes. The results showed that the strain difference in DNase II activity was controlled by a single autosomal locus. The locus for the mouse DNase II activity level, designated as Dnl2al, had at least two alleles. The allele Dnl2ala determines high DNase II activity and occurs in C57BL/6 and C3H/He strains. The other allele Dnl2alb determines low enzyme activity and occurs in BALB/c and DBA/2 strains.
对近交系小鼠的一项调查显示,脾脏、肝脏、肾脏、肺、心脏、凝固腺和包皮腺中的脱氧核糖核酸酶II(DNase II)活性存在遗传变异。由于这些组织中的DNase II活性彼此密切相关,因此提示该酶存在系统性调节。以脾脏DNase II活性水平作为子代表型指标,在测交中研究了DNase II活性定量变异的遗传情况。结果表明,DNase II活性的品系差异由一个常染色体位点控制。小鼠DNase II活性水平的位点命名为Dnl2al,至少有两个等位基因。等位基因Dnl2ala决定高DNase II活性,存在于C57BL/6和C3H/He品系中。另一个等位基因Dnl2alb决定低酶活性,存在于BALB/c和DBA/2品系中。