Jove
Visualize
お問い合わせ

関連する概念動画

Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.9K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
5.9K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.1K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
10.1K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.1K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
6.1K
Homologous Recombination02:31

Homologous Recombination

51.5K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
51.5K
The Replisome03:01

The Replisome

34.7K
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
34.7K
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

7.1K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
7.1K
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー
  1. ホーム
  2. ヒトのトランスレションdnaポリメラーゼrev1におけるpcna結合モチーフの特定とpcnaとの相互作用の構造的基礎
  1. ホーム
  2. ヒトのトランスレションdnaポリメラーゼrev1におけるpcna結合モチーフの特定とpcnaとの相互作用の構造的基礎

関連する実験動画

Analyzing DNA-Protein Interactions with Streptavidin-Based Biolayer Interferometry
08:07

Analyzing DNA-Protein Interactions with Streptavidin-Based Biolayer Interferometry

Published on: January 17, 2025

1.6K

ヒトのトランスレションDNAポリメラーゼREV1におけるPCNA結合モチーフの特定とPCNAとの相互作用の構造的基礎

Asami Hishiki1, Naoya Hoshino1, Kokona Okawara1

  • 1School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku Shizuoka, 422-8002, Japan.

Journal of biochemistry
|September 1, 2025

PubMed で要約を見る

まとめ
この要約は機械生成です。

REV1は,転移DNA合成 (TLS) に不可欠なDNAポリメラーゼであり,新たに特定されたモチーフを通じてPCNAと相互作用する. この研究は,REV1-PCNAの相互作用の構造的基礎を明らかにし,長年にわたる科学的議論を解決します.

キーワード:
PCNA についてPIPボックスREV1 についてクリスタル構造トランスレションDNA合成

さらに関連する動画

Identification of Nucleolar Factors During HIV-1 Replication Through Rev Immunoprecipitation and Mass Spectrometry
09:38

Identification of Nucleolar Factors During HIV-1 Replication Through Rev Immunoprecipitation and Mass Spectrometry

Published on: June 26, 2019

8.2K
Atomic Force Microscopy Investigations of DNA Lesion Recognition in Nucleotide Excision Repair
10:59

Atomic Force Microscopy Investigations of DNA Lesion Recognition in Nucleotide Excision Repair

Published on: May 24, 2017

9.6K

関連する実験動画

Analyzing DNA-Protein Interactions with Streptavidin-Based Biolayer Interferometry
08:07

Analyzing DNA-Protein Interactions with Streptavidin-Based Biolayer Interferometry

Published on: January 17, 2025

1.6K
Identification of Nucleolar Factors During HIV-1 Replication Through Rev Immunoprecipitation and Mass Spectrometry
09:38

Identification of Nucleolar Factors During HIV-1 Replication Through Rev Immunoprecipitation and Mass Spectrometry

Published on: June 26, 2019

8.2K
Atomic Force Microscopy Investigations of DNA Lesion Recognition in Nucleotide Excision Repair
10:59

Atomic Force Microscopy Investigations of DNA Lesion Recognition in Nucleotide Excision Repair

Published on: May 24, 2017

9.6K

科学分野:

  • 分子生物学
  • 生物化学
  • 遺伝学

背景:

  • REV1は,トランスレションDNA合成 (TLS) に不可欠な,誤りやすいY系DNAポリメラーゼである.
  • TLSはDNA複製を 損傷したテンプレートストランドを越えて進めるようにします
  • 増殖細胞核抗原 (PCNA) は,ユビキチン化時にTLSを刺激する支架タンパク質である.

研究 の 目的:

  • PCNA結合に責任を持つ REV1の特定の領域を特定する.
  • REV1 と PCNA の相互作用の構造的メカニズムを解明する.
  • REV1- PCNAの相互作用に関する以前の研究における不一致を解決する.

主な方法:

  • REV1における潜在的なPCNA結合モチーフを特定するための配列保存分析.
  • 人間のREV1-PCNA複合体の高解像度構造を決定するX線結晶学.
  • 相互作用を確認するために生化学分析.

主要な成果:

  • 脊椎動物のREV1シグネチャーシーケンスがPCNA結合に重要であることが確認された.
  • X線結晶学では,ヒトのREV1がPIPボックス変異体を通してPCNAを結合することを明らかにした.
  • この変種は,REV1の小指領域のC端側に位置しています.
  • 結論:

    • この研究は,REV1とPCNAの物理的な相互作用の決定的な構造的基礎を提供します.
    • この発見は,TLSの間にREV1が複製フォークに採用されるメカニズムを明確にします.
    • DNAの修復と複製の分野における 長年の論争を解決しました