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関連する概念動画

Regulated mRNA Transport02:22

Regulated mRNA Transport

6.9K
In eukaryotes, transcription and translation are compartmentalized; an mRNA is first synthesized in the nucleus and then selectively transported to the cytoplasm for protein synthesis. Before transport, a pre-mRNA undergoes several steps of post-transcriptional modifications including splicing, 5' capping, and the addition of a poly-adenine tail. Various proteins bind to the pre-mRNA during these modifications. The mRNA transport takes place with the help of multiple proteins playing...
6.9K
Regulated mRNA Transport02:22

Regulated mRNA Transport

3.3K
3.3K
Nuclear Export01:42

Nuclear Export

4.8K
The nucleus restricts several proteins within and allows others to pass. The restricted proteins possess a nuclear retention sequence or NRS, anchoring them to the nuclear lamins and preventing their transport to the cytosol. The non-restricted proteins, after their synthesis, are transported to their site of action, such as the cytosol or other organelles, with the help of nuclear export signals or NES.
NES are of three types- the canonical 10-residue long leucine-rich signal and other...
4.8K
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

8.6K
Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
8.6K
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

5.2K
5.2K
Directionality of Nuclear Transport01:42

Directionality of Nuclear Transport

4.5K
Ras-related nuclear protein or Ran is a small G protein that cycles between its GTP and GDP bound states. Ran specific regulators, a Ran GTPase Activating Protein or RanGAP present in the cytosol and a Ran guanine nucleotide exchange factor or RanGEF present inside the nucleus regulate GTP/GDP exchange. A high concentration of GTP inside the cells, in addition to this asymmetric distribution of  Ran-specific regulators, leads to a higher RanGTP concentration inside the nucleus. This...
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関連する実験動画

Updated: Jan 12, 2026

Analysis of mRNA Nuclear Export Kinetics in Mammalian Cells by Microinjection
11:32

Analysis of mRNA Nuclear Export Kinetics in Mammalian Cells by Microinjection

Published on: December 4, 2010

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ATPによる分子スイッチが人間のmRNAの輸出を指揮する.

Ulrich Hohmann1,2,3, Max Graf4,5, László Tirián6

  • 1Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria. u.hohmann@imb-mainz.de.

Nature
|November 6, 2025
PubMed
まとめ
この要約は機械生成です。

研究者らはヒトのmRNA輸出の分子メカニズムを発見し,ATPase UAP56を鍵となるスイッチとして特定しました. このATPアゼタンパク質は,トランスクリプション-エクスポート (TREX) コンプレックスから核毛孔コンプレックス (NPC) にメッセンジャーRNA (mRNA) を誘導して輸出する.

さらに関連する動画

Polysome Fractionation and Analysis of Mammalian Translatomes on a Genome-wide Scale
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Polysome Fractionation and Analysis of Mammalian Translatomes on a Genome-wide Scale

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Method for the Isolation and Identification of mRNAs, microRNAs and Protein Components of Ribonucleoprotein Complexes from Cell Extracts using RIP-Chip
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Method for the Isolation and Identification of mRNAs, microRNAs and Protein Components of Ribonucleoprotein Complexes from Cell Extracts using RIP-Chip

Published on: September 29, 2012

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関連する実験動画

Last Updated: Jan 12, 2026

Analysis of mRNA Nuclear Export Kinetics in Mammalian Cells by Microinjection
11:32

Analysis of mRNA Nuclear Export Kinetics in Mammalian Cells by Microinjection

Published on: December 4, 2010

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Polysome Fractionation and Analysis of Mammalian Translatomes on a Genome-wide Scale
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Polysome Fractionation and Analysis of Mammalian Translatomes on a Genome-wide Scale

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Method for the Isolation and Identification of mRNAs, microRNAs and Protein Components of Ribonucleoprotein Complexes from Cell Extracts using RIP-Chip
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Method for the Isolation and Identification of mRNAs, microRNAs and Protein Components of Ribonucleoprotein Complexes from Cell Extracts using RIP-Chip

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科学分野:

  • 分子生物学
  • 細胞生物学
  • 遺伝学

背景:

  • 伝達 RNA (mRNA) の核輸出は,真核生物の遺伝子発現に不可欠である.
  • mRNAをリボ核タンパク質複合体 (mRNP) に包装することは理解されているが,輸出プロセスは不明である.

研究 の 目的:

  • 人間のmRNAの輸出を制御する分子メカニズムを解明する.
  • 核の転写から核の輸出への移行に関与する主要なタンパク質と経路を特定する.

主な方法:

  • 生化学的測定法
  • 構造生物学技術
  • トランスクリプション-エクスポート複合体 (TREX) と核孔複合体 (NPC) の分析

主要な成果:

  • ATPase UAP56 (DDX39) をmRNAエクスポートにおける中心的な分子スイッチとして特定した.
  • UAP56は,ATP誘導のmRNA結合サイクルを介して,核プラズマのmRNPをTREXからNPCを固定したTREX-2複合体へと誘導する.
  • mRNP複合体の改造,NPCへのドッキング,そして輸出のためのリリース.

結論:

  • 一般的で進化的に保存されたmRNA輸出経路のためのメカニズム的枠組みを確立した.
  • この発見は,転写後のレベルでの遺伝子発現の調節に関する重要な洞察を提供します.