Guanine salvage by organ cultures of mouse tooth germs.

F J Dye
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Abstract

The effect of mycophenolic acid (MPA) which inhibits the biosynthesis of guanosine monophosphate (GMP) in organ cultures of mouse tooth germs can be partially counteracted by adding guanine to the MPA cultures. This may be due to salvaging guanine by the enzyme hypoxanthine guanine phosphoribosyl transferase (HGPRT), or to competition for a common membrane carrier involved in mediated transport of both guanine and hypoxanthine in normal biosynthesis and also of MPA. Experiments were carried out to compare the effect of either hypoxanthine or guanine on the MPA-caused inhibition. While addition of guanine to the MPA cultures (MPAG) supports growth equal to controls and development of dental-enamel junction (DEJ) to a level intermediate between control and MPA the addition of hypoxanthine (MPAHX) supports growth and DEJ development not better than MPA. This indicates that guanine is salvaged by HGPRT to GMP while hypoxanthine, salvaged to inosinic acid (inosinic monophosphate, IMP) is ineffective because the MPA inhibition is on the pathway from IMP to GMP.

小鼠牙齿细菌器官培养的鸟嘌呤回收。
在小鼠牙胚器官培养物中添加鸟嘌呤可以部分抵消霉酚酸(MPA)抑制鸟苷单磷酸(GMP)生物合成的作用。这可能是由于次黄嘌呤鸟嘌呤磷酸核糖基转移酶(HGPRT)对鸟嘌呤的回收,或者是由于在正常生物合成和MPA中参与鸟嘌呤和次黄嘌呤介导运输的共同膜载体的竞争。实验比较了次黄嘌呤和鸟嘌呤对mpa抑制作用的影响。在MPA培养物中添加鸟嘌呤(MPAG)对牙釉质结合部(DEJ)的生长和发育的支持程度与对照组相当,且介于对照组和MPA之间,而添加次黄嘌呤(MPAHX)对牙釉质结合部(DEJ)的支持程度不如MPA。这说明鸟嘌呤被HGPRT回收为GMP,而次黄嘌呤被回收为肌苷酸(肌苷单磷酸,IMP)是无效的,因为MPA抑制了从IMP到GMP的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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