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RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

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Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
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The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
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The writer...
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LTR Retrotransposons03:08

LTR Retrotransposons

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LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
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Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
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Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
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永続的な転写プログラムは,遠隔記憶と関連している.

Michelle B Chen1, Xian Jiang2,3, Stephen R Quake4,5

  • 1Department of Bioengineering, Stanford University, Stanford, CA, USA.

Nature
|November 12, 2020
PubMed
まとめ
この要約は機械生成です。

生涯続く遠隔記憶は 中間前頭前皮質の神経細胞の 持続的な遺伝子発現変化を含みます アストロサイトとマイクログリアも遺伝子発現の変化を示し,記憶の蓄積における彼らの積極的な役割を示しています.

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科学分野:

  • 神経科学
  • 分子生物学
  • 遺伝学

背景:

  • 短期記憶における遺伝子発現の役割は よく研究されています
  • 長期,生涯のリモートメモリストレージのメカニズムはほとんど不明です.
  • 前頭前皮質は 記憶の統合と回収に関与しています

研究 の 目的:

  • 遠隔記憶の単細胞遺伝子発現を調査する
  • 長期記憶の維持に伴う 分子機構を特定する
  • 遠隔記憶への 膠質細胞の貢献を探るため

主な方法:

  • マウスの長期恐怖記憶の パラダイムを利用した
  • 遺伝子発現を分析するために単細胞RNA配列を解析した.
  • 中部前頭皮質を分析した

主要な成果:

  • 学習後数週間で神経細胞に特異的な転写変化が確認された.
  • 記憶維持に潜在的に関与する 膜融合に関連する遺伝子を発見しました
  • 記憶と関連したアストロサイトとマイクログリアの持続的な遺伝子発現シグネチャーを観察した.

結論:

  • 遠隔記憶には 細胞型に特化した 持続的な遺伝子発現プログラムが含まれます
  • アストロサイトとマイクログリアを含むグリアル細胞は,遠隔記憶回路に積極的に参加する.
  • この発見は,活動に依存する細胞状態と記憶機構の理解に寄与する.