Vora S, Oskam R, Staal G E
Biochem J. 1985 Jul 15;229(2):333-41. doi: 10.1042/bj2290333.
In man and the rabbit, 6-phosphofructokinase (PFK, EC 2.7.1.11) exists in tetrameric isoenzymic forms composed of muscle (M or A), liver (L or B) and platelet or brain (P or C) subunits, which are under separate genetic control. In contrast, the genetic control of the rat PFK has not yet been conclusively established; it is unclear whether the P-type or C-type subunit exists in this species. To resolve this question, we investigated the enzyme from the skeletal muscle, liver and brain of rats of Wag/Rij strain. Our studies demonstrate that the rat PFK is also under the control of three structural loci and that the homotetramers M4, P4 and L4 exhibit unique chromatographic, immunological and kinetic-regulatory properties. Skeletal-muscle and brain PFKs consist of isolated M4 and P4 homotetramers respectively. Although liver PFK consists predominantly of L4 homotetramer, it also contains small amounts of PL3 and P2L2 species. All three PFKs exhibit allosteric properties: co-operativity with fructose 6-phosphate and inhibition by ATP decrease in the order P4 greater than L4 greater than M4. P4 and M4 tetramers are the most sensitive to citrate inhibition, whereas L4 tetramer is the least sensitive. More importantly, P4 and L4 isoenzymes are the most sensitive to activation by fructose 2,6-bisphosphate, whereas M4 isoenzyme is the least sensitive. These results indicate that the brain PFK in this strain of rat is a unique tetramer, P4, which also exhibits allosteric kinetics, as do the well-studied M4 and L4 isoenzymes. The reported differences in the number and nature of isoenzymes present in the rat brain and liver most probably reflect the differences in the strains studied by previous investigators. Since the nature of the rat PFK isoenzymes and nomenclatures reported by previous investigators have been now reconciled, it is proposed that, for the sake of uniformity, only well-established nomenclatures used for the rabbit or human PFK isoenzymes be used for the rat isoenzymes.
在人和兔子体内,6-磷酸果糖激酶(PFK,EC 2.7.1.11)以四聚体同工酶形式存在,由肌肉(M或A)、肝脏(L或B)以及血小板或脑(P或C)亚基组成,这些亚基受不同的基因控制。相比之下,大鼠PFK的基因控制尚未最终确定;该物种中是否存在P型或C型亚基尚不清楚。为了解决这个问题,我们研究了Wag/Rij品系大鼠的骨骼肌、肝脏和脑中的这种酶。我们的研究表明,大鼠PFK同样受三个结构基因座的控制,并且同四聚体M4、P4和L4表现出独特的色谱、免疫和动力学调节特性。骨骼肌和脑PFK分别由分离的M4和P4同四聚体组成。虽然肝脏PFK主要由L4同四聚体组成,但也含有少量的PL3和P2L2类型。所有三种PFK都表现出变构特性:对6-磷酸果糖的协同性以及对ATP的抑制作用按P4大于L4大于M4的顺序降低。P4和M4四聚体对柠檬酸抑制最敏感,而L4四聚体最不敏感。更重要的是,P4和L4同工酶对2,6-二磷酸果糖的激活最敏感,而M4同工酶最不敏感。这些结果表明,该品系大鼠脑中的PFK是一种独特的四聚体P4,它也表现出变构动力学,就像研究充分的M4和L4同工酶一样。先前研究人员报道的大鼠脑和肝脏中存在的同工酶数量和性质的差异很可能反映了先前研究的品系差异。由于先前研究人员报道的大鼠PFK同工酶的性质和命名法现在已经统一,因此建议为了统一起见,大鼠同工酶仅使用用于兔子或人类PFK同工酶的已确立的命名法。