Samollow P B, Vandeberg J L, Ford A L, Kunz H W, Gill T J
Genetics. 1986 Sep;114(1):247-58. doi: 10.1093/genetics/114.1.247.
Two recently identified isozymes of neuraminidase in rat liver were examined for transmission patterns and linkage relationships, and for variation among inbred strains. The isozymes, designated neuraminidase-1 (NEU-1) and neuraminidase-2 (NEU-2), exhibited no electrophoretic mobility variants among the 22 inbred strains examined, but did possess striking interstrain variation in activity phenotypes on electrophoretic gels. The results of a backcross analysis involving the KGH and ACP strains revealed that NEU-1 and NEU-2 phenotypes are independently controlled, each by a single autosomal locus with additively acting alleles. The two loci are unlinked to one another, but the gene controlling NEU-1 is tightly linked to RT1, the rat major histocompatibility complex. This gene is almost certainly identical to Neu-1, a gene identified previously through its effect on "total" activity levels of liver neuraminidase as determined by fluorometric assay of tissue homogenates. NEU-2 and the gene controlling its phenotype were not detected by the fluorometric technique. We designate the genes controlling the NEU-1 and NEU-2 phenotypes as Neu-1 and Neu-2, respectively. Data from this and other studies place Neu-1 between Glo-1 and dw-3. The location of Neu-2 is unknown.
对大鼠肝脏中最近发现的两种神经氨酸酶同工酶进行了遗传传递模式、连锁关系及近交系间差异的研究。这两种同工酶分别命名为神经氨酸酶-1(NEU-1)和神经氨酸酶-2(NEU-2),在所检测的22个近交系中未表现出电泳迁移率变异,但在电泳凝胶上的活性表型存在显著的品系间差异。涉及KGH和ACP品系的回交分析结果显示,NEU-1和NEU-2的表型由单个常染色体位点独立控制,每个位点的等位基因具有加性作用。这两个位点彼此不连锁,但控制NEU-1的基因与大鼠主要组织相容性复合体RT1紧密连锁。该基因几乎肯定与Neu-1相同,Neu-1是先前通过其对肝脏神经氨酸酶“总”活性水平的影响而鉴定的基因,该活性水平通过组织匀浆的荧光测定法确定。荧光技术未检测到NEU-2及其控制表型的基因。我们分别将控制NEU-1和NEU-2表型的基因命名为Neu-1和Neu-2。本研究及其他研究的数据表明Neu-1位于Glo-1和dw-3之间。Neu-2的位置未知。