Daniel W L, Harrison B W, Nelson K
J Hered. 1982 Jan-Feb;73(1):24-8. doi: 10.1093/oxfordjournals.jhered.a109569.
The ratio of hepatic arylsulfatase B activity of C57BL/6J, SWR/J, and A/J mice is approximately 5:2.5:1. The activity variation between SWR/J and A/J mice can be attributed to the effects of Asr-1, a cis-acting regulatory element near or within As-1 (arylsulfatase B structural locus). However, C57BL/6J and SWR/J mice share similar Asr-1 alleles and have comparable arylsulfatase B activities in nonhepatic tissues. The high arylsulfatase B activity occurring in C57BL/6J compared to SWR/J liver is largely determined by a site near Asr-1 and As-1. The C57BL/6J allele promotes a more prominent spike of liver arylsulfatase B activity at 12 days postnatal age and maintains a higher activity in the adult compared to SWR/J mice. This liver-specific genetic element exerts a trans effect and acts by affecting the accumulation of arylsulfatase B molecules in liver tissue.
C57BL/6J、SWR/J和A/J小鼠肝脏芳基硫酸酯酶B活性的比例约为5:2.5:1。SWR/J和A/J小鼠之间的活性差异可归因于Asr-1的作用,Asr-1是As-1(芳基硫酸酯酶B结构基因座)附近或内部的一个顺式作用调控元件。然而,C57BL/6J和SWR/J小鼠具有相似的Asr-1等位基因,且在非肝脏组织中具有相当的芳基硫酸酯酶B活性。与SWR/J肝脏相比,C57BL/6J肝脏中出现的高芳基硫酸酯酶B活性在很大程度上由Asr-1和As-1附近的一个位点决定。与SWR/J小鼠相比,C57BL/6J等位基因在出生后12天时促进肝脏芳基硫酸酯酶B活性出现更显著的峰值,并在成年期维持较高的活性。这种肝脏特异性遗传元件发挥反式作用,通过影响肝脏组织中芳基硫酸酯酶B分子的积累起作用。