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热激活的盘基网柄菌孢子萌发过程中核糖核酸合成的时间安排。

The timing of ribonucleic acid synthesis during the germination of heat-activated Dictyostelium discoideum spores.

作者信息

Hamer J E, Cotter D A

出版信息

Can J Microbiol. 1983 Oct;29(10):1390-8. doi: 10.1139/m83-214.

DOI:10.1139/m83-214
PMID:6661701
Abstract

To observe changes in the rate of RNA synthesis during Dictyostelium discoideum spore germination, we have pulse labeled germinating spores with [3H]uracil at stage-specific intervals. The labeled RNAs have been fractionated on 1.7 and 10% polyacrylamide gels. Additionally we have monitored the total changes in ribonucleic acid content during germination. In general, the rate of synthesis of various RNA species appears to increase noncoordinately, while the total RNA content remains unchanged during germination. This may indicate extensive RNA turnover during germination. Little or no RNA synthesis is observed during the first pulse period (postactivation lag). During the 1-2-h pulse period, 25, 17, 5.8, and 5 S RNA were all synthesized. The synthesis of these species increased with each pulse period, with the greatest amount of synthesis occurring during the final 3-4-h pulse. The synthesis of 4 S RNA initiated during the 2-3-h pulse and increased during the final 3-4-h pulse. The percentage of poly(A) + RNA increased with each time period from 0.1% of the total labeled RNA at the 0-1-h pulse period to 10% of the total RNA synthesized at the 2-3-h pulse time. During the final pulse period (3-4 h), this level dropped to 6%. Analysis of acid-soluble extracts from dormant spores revealed relatively high levels of the four ribonucleoside 5'-triphosphates. These levels remained unchanged during the 1st h of germination. Thus RNA synthesis during the postactivation lag stage of germination does not appear to be limited by precursor availability and may involve other regulatory mechanisms.

摘要

为了观察盘基网柄菌孢子萌发过程中RNA合成速率的变化,我们在特定阶段间隔用[3H]尿嘧啶对萌发的孢子进行脉冲标记。标记的RNA已在1.7%和10%的聚丙烯酰胺凝胶上进行分级分离。此外,我们还监测了萌发过程中核糖核酸含量的总体变化。一般来说,各种RNA种类的合成速率似乎是非协同增加的,而总RNA含量在萌发过程中保持不变。这可能表明萌发过程中存在广泛的RNA周转。在第一个脉冲期(激活后延迟期)几乎没有观察到RNA合成。在1-2小时的脉冲期内,25S、17S、5.8S和5S RNA均有合成。这些种类的合成随着每个脉冲期而增加,在最后3-4小时的脉冲期合成量最大。4S RNA的合成在2-3小时的脉冲期开始,并在最后3-4小时的脉冲期增加。多聚腺苷酸(poly(A)+)RNA的百分比随每个时间段增加,从0-1小时脉冲期占总标记RNA的0.1%增加到2-3小时脉冲期合成的总RNA的10%。在最后一个脉冲期(3-4小时),这个水平降至6%。对休眠孢子的酸溶性提取物分析显示,四种核糖核苷5'-三磷酸水平相对较高。这些水平在萌发的第1小时内保持不变。因此,萌发激活后延迟阶段的RNA合成似乎不受前体可用性的限制,可能涉及其他调节机制。

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