Kokunin V A, Tkachuk O M, Guliĭ M F
Ukr Biokhim Zh. 1977 May-Jun;49(3):76-9.
Maximum incorporation of the label after administration of 14C-bicarbonate to free pyrimidine nucleotides begins by the 60th minute. Radioactivity of cytidine nucleotides at all time points is four-eight times as low as that of uridine nucleotides. 2-14C-orotic acid is incorporated into acid-soluble nucleotides and RNA of the liver and spleen tissues. 60 min after administration of the isotope 20% of radioactivity was found in the liver and 0.3% in the spleen, in both tissues radioactivity of RNA is 20% of 14C-radioactivity in the acid-soluble fraction. The formation rate for cytidine nucleotides from uridine ones in the liver and spleen tissues is low, about 2-6% of uridine nucleotides radioactivity is found in them only, that may be due to a low activity of CTP-synthetase. The content of cytidine nucleotides in these organs is three-life times as low as compared to uridine nucleotides.
给游离嘧啶核苷酸注射14C - 碳酸氢盐后,到第60分钟时标记物的掺入量达到最大值。在所有时间点,胞苷酸的放射性都比尿苷酸低4至8倍。2 - 14C - 乳清酸被掺入肝脏和脾脏组织的酸溶性核苷酸及RNA中。注射同位素60分钟后,在肝脏中发现20%的放射性,在脾脏中为0.3%,在这两种组织中,RNA的放射性是酸溶性部分中14C - 放射性的20%。肝脏和脾脏组织中由尿苷酸形成胞苷酸的速率较低,仅在其中发现约2 - 6%的尿苷酸放射性,这可能是由于CTP合成酶活性较低所致。这些器官中胞苷酸的含量比尿苷酸低三至五倍。