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Faster synthesis and slower degradation of liver protein during developmental growth.

机译:发育过程中肝蛋白合成更快降解更慢。

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摘要

A study is presented of the liver protein gain during the early stages of postnatal development. Fractional rates of protein synthesis and degradation were determined in vivo in livers of 4-day-old mice. At this age, liver protein accumulated at a rate of 18% per day. Synthesis was measured after the injection of massive amounts of radioactive leucine. Degradation was extimated as the balance between synthesis and accumulation of stable liver proteins, or from the disappearance of radioactivity from liver protein previously labelled by the administration of NaH14CO3. We found that the neonatal livers: (1) synthesize 139% as much protein per unit time and unit mass as adult tissue, which is accounted for by a higher ribosome concentration (synthesis per mg of RNA was the same); (2) retain 39% of the newly synthesized protein as stable liver components (compared with 48% in adult mice); (3) degrade protein at 56% of the rate in the adult liver. This lower rate of degradation is quantitatively the most significant difference between the growing and non-growing liver.
机译:一项有关出生后早期肝脏蛋白质增加的研究被提出。在4日龄小鼠的肝脏中,体内测定了蛋白质合成和降解的分数速率。在这个年龄,肝蛋白每天以18%的速度积累。注射大量放射性亮氨酸后测量合成。降解被认为是稳定的肝蛋白合成与积累之间的平衡,或者是由于先前通过施用NaH14CO3标记的肝蛋白中放射性的消失所致。我们发现新生儿肝脏:(1)单位时间和单位质量的蛋白质含量是成人组织的139%,这是由于核糖体浓度较高(每毫克RNA的合成量相同)所致; (2)保留39%的新合成蛋白质作为稳定的肝脏成分(成年小鼠中则保留48%); (3)在成人肝脏中以56%的速度降解蛋白质。从数量上讲,这种较低的降解速度是正在生长的肝脏和未生长的肝脏之间最大的区别。

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