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再生核质体中的程序化大分子合成

Programmed macromolecular synthesis in regenerating karyoplasts.

作者信息

White J D, Bruno J, Lucas J J

出版信息

Mol Cell Biol. 1983 Oct;3(10):1866-81. doi: 10.1128/mcb.3.10.1866-1881.1983.

Abstract

Conditions for the preparation, purification, and maintenance of karyoplasts which could regenerate to reform whole viable cells were defined. Results of biochemical analyses of such karyoplasts at various times during regeneration indicated that a reproducible biosynthetic program was followed. Thus, an examination of the polypeptides made during regeneration by two-dimensional gel electrophoresis showed that the pattern of radiolabeled polypeptides synthesized at each time studied was specific and was significantly different from that observed at other times during regeneration. Polypeptides associated with three major cellular fractions--nuclear, cytoskeletal-microtrabecular, and soluble--were among the most dramatically regulated molecules. Other polypeptides, such as the major components of microfilaments and intermediate filaments, were synthesized at relatively constant rates and were assembled into structures throughout regeneration. Likewise, microtubules appeared to be reformed throughout regeneration, even in the absence of identifiable centriole-associated organizing centers. Finally, analysis of DNA synthesis by autoradiography showed that, even when prepared from whole cells synchronized at the G1/S interface, karyoplasts could not begin making DNA until they had regenerated an almost complete complement of cytoplasm.

摘要

确定了制备、纯化和维持能够再生以重新形成完整活细胞的核质体的条件。对再生过程中不同时间的此类核质体进行生化分析的结果表明,遵循了可重复的生物合成程序。因此,通过二维凝胶电泳对再生过程中产生的多肽进行检查发现,在每个研究时间合成的放射性标记多肽模式是特定的,并且与再生过程中其他时间观察到的模式有显著差异。与三种主要细胞组分(核、细胞骨架 - 微梁和可溶性组分)相关的多肽是调控最为显著的分子之一。其他多肽,如微丝和中间丝的主要成分,以相对恒定的速率合成,并在整个再生过程中组装成结构。同样,微管似乎在整个再生过程中重新形成,即使在没有可识别的中心粒相关组织中心的情况下也是如此。最后,通过放射自显影分析DNA合成表明,即使从在G1/S界面同步的全细胞制备核质体,核质体在再生出几乎完整的细胞质补充之前也无法开始合成DNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a0/370048/3f8a50de6c48/molcellb00110-0193-a.jpg

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