Sakiyama T
Department of 1st Pathology, St. Marianna University School of Medicine.
Nihon Rinsho. 1996 Dec;54(12):3220-5.
PNP, encoded by 6 exons on human chromosome 14q13, is a homotrimetic enzyme of approximately 96 k dalton. This enzyme reversibly catalyzes the phosphorolysis of purine nucleoside to their respective purine bases and the corresponding pentose-1-phosphate. The ultimate degradative product of purine nucleoside is uric acid, which is a depleted product with the absence of PNP activity. This leads to accumulation of deoxy-guanosine triphosphate, which inhibits the enzyme ribonucleoside reductase resulting in DNA synthesis block and T cell proliferation. Basic and brief knowledge of PNP biochemistry and functional physiology is summarized for the understanding of clinical features of PNP deficiency.
嘌呤核苷磷酸化酶(PNP)由人类14号染色体q13上的6个外显子编码,是一种分子量约为96千道尔顿的同三聚体酶。该酶可逆地催化嘌呤核苷磷酸解为各自的嘌呤碱基和相应的磷酸戊糖。嘌呤核苷的最终降解产物是尿酸,在缺乏PNP活性时是一种消耗产物。这会导致脱氧三磷酸鸟苷积累,抑制核糖核苷还原酶,从而导致DNA合成受阻和T细胞增殖。为了理解PNP缺乏的临床特征,总结了PNP生物化学和功能生理学的基础及简要知识。