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在金鱼视神经再生过程中,转运核糖核酸可能会通过轴突运输。

Transfer RNA may be axonally transported during regeneration of goldfish optic nerves.

作者信息

Ingoglia N A, Tuliszewski T

出版信息

Brain Res. 1976 Aug 13;112(2):371-81. doi: 10.1016/0006-8993(76)90291-2.

Abstract

If [3H]uridine is injected into the eyes of goldfish during optic nerve regeneration, then the return of fibers to the optic tectum is accompanied by the appearance of [3H]RNA in the tectum. The amount of [3H]RNA arriving in the tectum is consistently greater than in non-regenerating controls and reaches maximum levels (more than 10 times controls) 24 days after optic nerve crush. When [14C]uridine is injected subarachnoidally 1 day prior to sacrificing, the amount of [14C]RNA in the tectum is approximately doubled throughout the regeneration period. In order to characterize the radioactive tectal RNA in these experiments, we have crushed the optic nerves of 15 fish, and 18 days later injected [3H]uridine into both eyes. Five days later [14C]uridine was injected subarachnoidally and all fish were sacrificed a day later. RNA was extracted and fractionated in 2.0% polyacrylamide gels. The amounts of 3H- and 14C-labeled ribosomal as well as small molecular weight RNAs were increased during regeneration. Analysis of the area under the 28S, 18S and 4-7S RNA peaks indicated a small increase in 14C radioactivity in each peak (1.2, 1.5, and 1.5 times control, respectively). On the other hand, 3H radioactivity showed the greatest increase in the 4-7S fraction (8.0 times control) whereas large molecular weight ribosomal fractions were approximately 3 times control. Electrophoresis of the RNA on 10% polyacrylamide gels demonstrated that all of the small molecular weight RNA was confined to the 4S (tRNA) peak. These results suggest that when optic nerves of goldfish regenerate, they may enter the tectum carrying 4S (transfer) RNA.

摘要

如果在视神经再生过程中向金鱼眼中注射[3H]尿苷,那么纤维回到视顶盖时,视顶盖中会出现[3H]RNA。到达视顶盖的[3H]RNA量始终大于未再生对照组,在视神经挤压后24天达到最高水平(超过对照组10倍)。在处死前1天蛛网膜下注射[14C]尿苷,在整个再生期间视顶盖中[14C]RNA量大约翻倍。为了在这些实验中表征放射性视顶盖RNA,我们挤压了15条鱼的视神经,18天后向双眼注射[3H]尿苷。5天后蛛网膜下注射[14C]尿苷,1天后处死所有鱼。提取RNA并在2.0%聚丙烯酰胺凝胶中分级分离。再生期间3H和14C标记的核糖体RNA以及小分子RNA量增加。对28S、18S和4 - 7S RNA峰下面积分析表明每个峰中14C放射性有小幅增加(分别为对照组的1.2、1.5和1.5倍)。另一方面,3H放射性在4 - 7S组分中增加最多(为对照组的8.0倍),而大分子核糖体组分约为对照组的3倍。RNA在10%聚丙烯酰胺凝胶上电泳表明所有小分子RNA都集中在4S(tRNA)峰。这些结果表明,金鱼视神经再生时,可能携带4S(转移)RNA进入视顶盖。

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