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相关概念视频

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During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
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Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
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The Unfolded Protein Response01:37

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The ER is the hub of protein synthesis in a cell. It has robust systems to quality control protein folding and also for degradation of terminally misfolded proteins. Under normal conditions, a small proportion of misfolded proteins that cannot be salvaged need to be transported to the cytoplasm by the ER-associated degradation or ERAD pathways. However, if the ERAD cannot handle the misfolded proteins, the cell activates the unfolded protein response or UPR to adjust the protein folding...
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Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
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Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

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The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the...
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Gene expression can be regulated at almost every step from gene to protein. Transcription is the step that is most commonly regulated. This involves the binding of proteins to short regulatory sequences on the DNA. This association can either promote or inhibit the transcription of a gene associated with the respective sequence.
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相关实验视频

Updated: Jun 29, 2025

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神经元活动通过eIF4G2:uORF结合快速重新编程树突翻译.

Ezgi Hacisuleyman1, Caryn R Hale2,3, Natalie Noble2

  • 1Laboratory of Molecular Neuro-oncology, The Rockefeller University, New York, NY, USA. fhacisuley@rockefeller.edu.

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概括
此摘要是机器生成的。

神经元在学习过程中迅速改变蛋白质表达. 上游开放阅读框架 (uORF) 的活动依赖翻译由eIF4G2控制局部蛋白质合成,将神经元活动与树突重塑联系起来.

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科学领域:

  • 神经科学是一个神经科学.
  • 分子生物学分子生物学
  • 细胞生物学 细胞生物学

背景情况:

  • 学习和记忆取决于活动诱导的树突翻译变化.
  • 涉及的特定mRNA及其调节机制在很大程度上仍然未知.

研究的目的:

  • 研究神经元脱极化如何影响局部树突生物学.
  • 为了识别由树突中神经元活动调节的mRNA和蛋白质.

主要方法:

  • 树突向的近距离标签,其次是交叉链接的免疫沉.
  • 用核糖体分析和质谱学来分析翻译变化.
  • 主要皮层神经元被使用KCl或DHPG去极化.

主要成果:

  • 神经元脱极化迅速重新编程树突蛋白质表达,mRNA和蛋白质变化之间的相关性较弱.
  • 脱极化增强了上游开放阅读框架 (uORF) 和特定mRNA的下游序列的翻译.
  • 这一过程涉及酸化和翻译启动因子eIF4G2的招募,使局部蛋白质合成成为可能.

结论:

  • 通过eIF4G2对uORF的活动依赖翻译是将神经元活动与局部树突重塑联系起来的关键机制.
  • 这一途径调节了对长期增强,细胞信号和能量代谢至关重要的蛋白质的产生.