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関連する概念動画

The Central Dogma01:25

The Central Dogma

116.7K
Overview
116.7K
pre-mRNA Processing02:01

pre-mRNA Processing

49.0K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
49.0K
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

19.9K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
19.9K
Leaky Scanning02:28

Leaky Scanning

4.5K
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...
4.5K
Rab Proteins01:14

Rab Proteins

4.0K
Rab proteins constitute the largest family of monomeric GTPases, of which 70 members are present in humans. Rab proteins and their effectors regulate consecutive stages of vesicle transport such as vesicle transport, docking, and fusion to the correct recipient membrane.
Rab proteins switch between a cytosolic, GDP-bound inactive state and a membrane-anchored, GTP-bound active state. By themselves, Rabs show slow rates of GDP/GTP exchange and GTP hydrolysis. Thus, Rab proteins are considered...
4.0K
The Central Dogma01:20

The Central Dogma

21.2K
The central dogma explains the flow of genetic information from DNA nucleotides to the amino acid sequence of proteins.
RNA is the Missing Link Between DNA and Proteins
In the early 1900s, scientists discovered that DNA stores all the information needed for cellular functions and that proteins perform most of these functions. However, the mechanisms of converting genetic information into functional proteins remained unknown for many years. Initially, it was believed that a single gene is...
21.2K

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関連する実験動画

Updated: May 5, 2026

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp
10:44

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ウサギのアルファグロービンmRNAのプライマリ配列.

H C Heindell, A Liu, G V Paddock

    Cell
    |September 1, 1978
    PubMed
    まとめ

    研究者らは,ウサギのアルファグロービンメッセンジャーRNA (mRNA) の完全な配列を解析し,補完RNA (cRNA) 配列を解析することによってその正確性を確認しました. この詳細な配列は,遺伝子発現とタンパク質合成の洞察を提供します.

    科学分野:

    • 分子生物学は分子生物学である.
    • 遺伝学 遺伝学とは
    • バイオケミストリー バイオケミストリー

    背景:

    • ウサギのアルファグロービン遺伝子は,ヘモグロビン生産に不可欠です.
    • 伝達 RNA (mRNA) の正確な配列は,遺伝子発現とタンパク質合成を理解するために不可欠です.

    研究 の 目的:

    • ウサギのアルファグロービンメッセンジャーRNA (mRNA) の完全なヌクレオチド配列を決定する.
    • 配列化されたmRNAの精度を,既存のデータと補完的なRNA (cRNA) 配列の比較を通じて検証する.
    • 塩基構成とコドン偏好を含むmRNA配列の一般的な特徴を分析する.

    主な方法:

    • マクサムとギルバート法によるDNAシーケンシング.
    • ウサギのアルファグロービンDNA挿入を含むキメリックプラズミドpHb 72の分析.
    • 取得したmRNA配列の比較と,5'端と3'端に関する以前に公表されたデータ.
    • 新しいコンピュータプログラムを使用して,塩基配列の配列を分析する.

    主要な成果:

    • ウサギのアルファグロービンmRNAの完全なプライマリ配列が決定され,最初の361の翻訳されたヌクレオチドを通して5'翻訳されていない領域を網羅しました.

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    Use of Alu Element Containing Minigenes to Analyze Circular RNAs
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    In Vitro Generation of Somite Derivatives from Human Induced Pluripotent Stem Cells
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  • 決定された配列は,以前に報告された重複する配列と完全に一致していました.
  • 結果は,in vitroで合成された遺伝子のコピー,細菌のクローン,およびメンテナンスの高信頼性を再確認しました.
  • 結論:

    • ウサギのアルファグロービンmRNAの完全な配列は,高精度で確立されています.
    • この発見は,合成,クローン,およびインビトロにおける遺伝子コピー保持の信頼性を裏付けている.
    • 配列の分析は,遺伝子発現,コドン使用,mRNA構造を理解するための貴重なデータを提供します.