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[藻状菌丛枝状全毛菌发育的研究。III. 配子囊分化过程中的多核糖体形成和RNA代谢(作者译)]

[Studies on development of the phycomycete Allomyces arbuscula. III. Polysome formation and RNA metabolism during differentiation of gametangia (author's transl)].

作者信息

Fähnrich P

出版信息

Arch Microbiol. 1977 Apr 1;112(3):255-61. doi: 10.1007/BF00413089.

Abstract

Polysomes were isolated both from growing gametophytes of Allomyces arbuscula and from gametangia prepared from mycelia at different periods during gametogenesis. Analysis of polysomes by sucrose gradients showed that ribosomes present in the gametangia monosome pool were shifted into polysomes. This shift was found to be correlated with gametangia differentiation. The ribosome distribution remained virtually unchanged during the early stage of gamete formation. In mature gametes and swarming zygotes a low level of polysomes was detected. Labeling of rRNA by 32PO4 demonstrated a de novo synthesis of monosomes throughout the period of gametangia differentiation. No incorporation of 32PO4 was found to be present in ribosomes prepared from gametangia after onset of gamete formation. On the basis of these labeling experiments it is concluded that radioactivity in polysomes extracted from mature gametes and swarming zygotes can be attributed in part to conserved mRNA. Synchronous formation of gametangia was induced by transferring the vegetative mycelia from growth medium into a low salt buffer. Under these conditions the incorporation of either 32PO4 or 3H-uridine into RNA, particularly into rRNA, was found to be markedly decreased. This obviously indicates a shutdown of RNA synthesis. rRNA from induced mycelia examined by polyacrylamide gel electrophoresis was found to be severely degraded. In contrast to this, rRNA isolated from ribosomes of developing gametangia and from gametes exhibited no degradation products. It is suggested that endonucleases cause rRNA hydrolysis in the hyphal cytoplasm during gametangia differentiation. Ribosomes compartmentalized in gametangia seem to be inaccessible to nucleases during the later process for gametogenesis.

摘要

多核糖体是从丛枝状异水霉正在生长的配子体以及从配子发生过程中不同时期的菌丝体制备的配子囊中分离出来的。通过蔗糖梯度对多核糖体进行分析表明,存在于配子囊单体池中的核糖体转移到了多核糖体中。发现这种转移与配子囊分化相关。在配子形成的早期阶段,核糖体分布几乎保持不变。在成熟配子和游动合子中检测到低水平的多核糖体。用³²PO₄标记rRNA表明,在配子囊分化的整个时期都有单体的从头合成。在配子形成开始后,从配子囊中制备的核糖体中未发现³²PO₄的掺入。基于这些标记实验得出结论,从成熟配子和游动合子中提取的多核糖体中的放射性部分可归因于保守的mRNA。通过将营养菌丝体从生长培养基转移到低盐缓冲液中诱导配子囊同步形成。在这些条件下,发现³²PO₄或³H - 尿苷掺入RNA,特别是掺入rRNA的量明显减少。这显然表明RNA合成停止。通过聚丙烯酰胺凝胶电泳检查诱导菌丝体的rRNA,发现其严重降解。与此相反,从发育中的配子囊核糖体和配子中分离的rRNA没有显示出降解产物。有人认为,在配子囊分化过程中,内切核酸酶会导致菌丝细胞质中的rRNA水解。在配子发生的后期过程中,分隔在配子囊中的核糖体似乎对内切核酸酶不可接近。

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