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関連する概念動画

Co-activators and Co-repressors02:04

Co-activators and Co-repressors

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Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
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Cooperative Binding of Transcription Regulators02:13

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Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form...
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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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Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
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転写 調節 器 は 複製 後 の 核 細胞 と 競合 する

Srinivas Ramachandran1, Steven Henikoff1

  • 1Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Howard Hughes Medical Institute, Seattle, WA 98109, USA.

Cell
|April 12, 2016
PubMed
まとめ

染色体組織は,転写因子,RNAポリメラーゼII,およびリモデラーの作用により,DNA複製後に復元される. この研究は 核細胞が複製から数分後に 再現される様子を明らかにしています

科学分野:

  • 分子生物学
  • 遺伝学
  • エピジェネティクス

背景:

  • DNA複製には 核分裂と再構成が必要です
  • 複製後のクロマチンの回復のメカニズムは不明である.

研究 の 目的:

  • DNA複製後に全ゲノムにわたるクロマチンの組織がどのように再構築されるかを調査する.
  • 複製フォークの背後にある核細胞とタンパク質の位置を特徴づける.

主な方法:

  • 開発されたMapping In vivo 新生染色体とEDUとシーケンシング (MINCE-seq).
  • MINCE-seqは,クロマチンの複製後の高時間的および空間的な解像度を提供します.

主要な成果:

  • 複製は,ドロソフィラのプロモーターとエンハンスターの特徴的なクロマチンの風景を乱します.
  • 高いRNAPIIの停滞とプロモーターのDNAアクセシビリティはBRMリモデラーの濃縮と相関する.
  • 強化染色体の破壊は,核細胞の再構築におけるTF競争を示唆する.

結論:

  • この研究は,複製後の核群の急速な再出現を明らかにしている.

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Describing a Transcription Factor Dependent Regulation of the MicroRNA Transcriptome
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  • 転写因子,RNAPII,およびリモデラーは,クロマチンの組織を回復する上で重要な役割を果たします.
  • 複製から数分後には 特徴的な風景に変わります