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大鼠B - 50基因的转录与翻译。

Rat B-50 gene transcription and translation.

作者信息

Eggen B J, Brandsma D, Kasperaitis M, Gispen W H, Schrama L H

机构信息

Laboratory for Physiological Chemistry, Rudolf Magnus Institute for Neurosciences, Utrecht University, The Netherlands.

出版信息

Brain Res. 1995 Aug 28;690(1):73-81. doi: 10.1016/0006-8993(95)00589-i.

Abstract

Previously we reported that the rat B-50/GAP-43 gene contains two promoters (P1 and P2). This study describes the contribution of these two promoters to the mRNA population in several paradigms leading to an altered B-50 mRNA expression. In 8-day-old rat brain we found that P1 transcripts (1676 +/- 50 nt) account for 5% and P2 transcripts (1462 +/- 46 nt) for 95% of the B-50 mRNAs. The expression of P1 and P2 derived transcripts is high at postnatal day 8 and the ratio between the amount of transcripts derived from P1 and P2 did not change during (embryonal and postnatal) development or aging. After peripheral nerve crush or transection B-50 mRNA expression in induced in the distal nerve stump. The amount of transcript in the nerve stump distal of the lesion derived from both P1 and P2 was increased and the ratio between P1 and P2 transcripts was not altered. To determine whether both P1 and P2 transcripts are translated, a polyribosomal profile from 8-day-old rat brain was generated. Northern analysis showed that both transcripts were associated with approximately four ribosomes. Since no change could be found in the activity in either of the two promoters under the different circumstances tested, we conclude that the activity of the two rat B-50 gene promoters is regulated by a similar mechanism.

摘要

此前我们报道,大鼠B-50/GAP-43基因包含两个启动子(P1和P2)。本研究描述了在几种导致B-50 mRNA表达改变的模式中,这两个启动子对mRNA群体的贡献。在8日龄大鼠脑中,我们发现P1转录本(1676 +/- 50 nt)占B-50 mRNA的5%,P2转录本(1462 +/- 46 nt)占95%。在出生后第8天,源自P1和P2的转录本表达很高,并且在(胚胎期和出生后)发育或衰老过程中,源自P1和P2的转录本数量之比没有变化。在周围神经挤压或横断后,损伤远端神经残端中诱导产生B-50 mRNA表达。损伤远端神经残端中源自P1和P2的转录本数量均增加,且P1和P2转录本之比未改变。为了确定P1和P2转录本是否都被翻译,我们制备了8日龄大鼠脑的多核糖体图谱。Northern分析表明,这两种转录本都与大约四个核糖体相关联。由于在测试的不同情况下,两个启动子中的任何一个的活性均未发现变化,我们得出结论,大鼠B-50基因的两个启动子的活性受相似机制调控。

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