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多头绒泡菌在饥饿和形成小球期间核酸与蛋白质合成的变化

Changes in nucleic acid and protein synthesis during starvation and spherule formation inPhysarum polycephalum.

作者信息

Sauer H W, Babcock K L, Rusch H P

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin Medical Center, 53706, Madison, Wisconsin.

Zoologisches Institut der Universität, Berliner Str. 15, D-6900, Heidelberg.

出版信息

Wilhelm Roux Arch Entwickl Mech Org. 1970 Jun;165(2):110-124. doi: 10.1007/BF00650140.

Abstract

The synthesis of protein and nucleic acids was studied by isotope incorporation and dilution in the plasmodia ofPhysarum polycephalum during periods of growth and differentiation (spherule formation). The total protein content decreased during starvation, but protein synthesis still occurred, probably at the expense of proteins previously synthesized during growth. Studies on leucine incorporation showed that protein synthesized during growth had a greater turnover than did protein formed by starving cultures, when both types of cultures were transferred to starvation conditions. Protein synthesis after prolonged starvation was rapidly and markedly decreased following the inhibition of RNA synthesis, whereas no such direct dependence on RNA synthesis was observed in growing cultures or during early starvation.The kinetics of RNA synthesis and the types of RNA formed were also shown to differ in growth and starvation. RNA turnover was low in growing cultures but substantial in starving cultures that were returned to growth medium. Qualitative differences in pulse-labeled RNA extracted from growing or starving cultures were revealed by methylated-albumin-kieselguhr column chromatography and sucrose gradient centrifugation. In starving cultures proportionately more labeled RNA was found in the lighter, non-ribosomal region of the gradient, and RNA from this region hybridized with denatured DNA to a greater extent than did other RNA fractions.

摘要

在多头绒泡菌的原质团生长和分化(形成小球体)期间,通过同位素掺入和稀释研究了蛋白质和核酸的合成。饥饿期间总蛋白质含量下降,但蛋白质合成仍在进行,可能是以生长期间先前合成的蛋白质为代价。对亮氨酸掺入的研究表明,当将两种类型的培养物转移到饥饿条件下时,生长期间合成的蛋白质比饥饿培养物形成的蛋白质具有更高的周转率。长时间饥饿后的蛋白质合成在RNA合成受到抑制后迅速且显著下降,而在生长的培养物或早期饥饿期间未观察到对RNA合成的这种直接依赖性。RNA合成的动力学以及形成的RNA类型在生长和饥饿过程中也有所不同。生长中的培养物中RNA周转率较低,但回到生长培养基的饥饿培养物中RNA周转率较高。通过甲基化白蛋白-硅藻土柱色谱法和蔗糖梯度离心法揭示了从生长或饥饿培养物中提取的脉冲标记RNA的定性差异。在饥饿培养物中,在梯度较轻的非核糖体区域发现了比例更高的标记RNA,并且该区域的RNA与变性DNA的杂交程度比其他RNA组分更大。

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