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通过核糖体密度图谱(RDM)检测核糖体与mRNA 5'前导序列的结合。

Detecting ribosomal association with the 5' leader of mRNAs by Ribosome Density Mapping (RDM).

作者信息

Eldad Naama, Arava Yoav

机构信息

Department of Biology, Technion--Israel Institute of Technology, Haifa, Israel.

出版信息

Methods Enzymol. 2007;431:163-75. doi: 10.1016/S0076-6879(07)31009-4.

Abstract

In eukaryotes, scanning of the 5' leader by the small ribosomal subunit precedes recognition of the start codon. Thus, various sequence elements that are located within this region may affect ribosomes' progression and lead to significant effects on translation. Most notable are short ORFs located upstream of the start codon, which are known to regulate the translation of the main ORF in the transcript. The function of these elements is likely to correlate with altered ribosomal association with the 5' leader of the mRNA. Currently, the only method to determine the ribosomal association of different regions of the mRNA in vivo is the Ribosome Density Mapping (RDM) procedure. This method entails cleavage of the target mRNA by specific oligodeoxynucleotides and RNase H and separation of the cleavage products by velocity sedimentation in a sucrose gradient. In this chapter, we provide a detailed protocol for this procedure and discuss its feasibility.

摘要

在真核生物中,小核糖体亚基对5'前导序列的扫描先于起始密码子的识别。因此,位于该区域内的各种序列元件可能会影响核糖体的进程,并对翻译产生显著影响。最值得注意的是位于起始密码子上游的短开放阅读框,已知它们可调节转录本中主要开放阅读框的翻译。这些元件的功能可能与核糖体与mRNA的5'前导序列结合的改变有关。目前,在体内确定mRNA不同区域核糖体结合情况的唯一方法是核糖体密度图谱(RDM)程序。该方法需要用特定的寡脱氧核苷酸和核糖核酸酶H切割目标mRNA,并通过在蔗糖梯度中进行速度沉降来分离切割产物。在本章中,我们提供了该程序的详细方案并讨论了其可行性。

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