Jove
Visualize
お問い合わせ
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

関連する概念動画

Forces Acting on Chromosomes02:11

Forces Acting on Chromosomes

During mitosis, chromosome movements occur through the interplay of multiple piconewton level forces. In prometaphase, these forces help in chromosome assembly or congression at the equatorial plane, eventually leading to their alignment at the metaphase plate. The forces acting on the chromosomes are space and time-dependent; therefore, they vary with the position of the chromosomes as the cell progresses through mitosis. 
Microtubules and motor proteins exert two types of forces on...
Forces Acting on Chromosomes02:11

Forces Acting on Chromosomes

During mitosis, chromosome movements occur through the interplay of multiple piconewton level forces. In prometaphase, these forces help in chromosome assembly or congression at the equatorial plane, eventually leading to their alignment at the metaphase plate. The forces acting on the chromosomes are space and time-dependent; therefore, they vary with the position of the chromosomes as the cell progresses through mitosis. 
Microtubules and motor proteins exert two types of forces on...
The Spindle Assembly Checkpoint02:19

The Spindle Assembly Checkpoint

The spindle assembly checkpoint is a molecular surveillance mechanism ensuring the fidelity of chromosome segregation during anaphase. The checkpoint monitors the completion of all the prerequisite steps before chromosome segregation to determine whether the segregation process should proceed or be delayed.
Many proteins function together to control the spindle assembly checkpoint. Mutations affecting these proteins may allow cells to proceed into anaphase prematurely, resulting in the...
The Spindle Assembly Checkpoint02:19

The Spindle Assembly Checkpoint

The spindle assembly checkpoint is a molecular surveillance mechanism ensuring the fidelity of chromosome segregation during anaphase. The checkpoint monitors the completion of all the prerequisite steps before chromosome segregation to determine whether the segregation process should proceed or be delayed.
Many proteins function together to control the spindle assembly checkpoint. Mutations affecting these proteins may allow cells to proceed into anaphase prematurely, resulting in the...
Anaphase A and B01:39

Anaphase A and B

Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
Spindle Assembly02:50

Spindle Assembly

Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a microtubule array...

こちらも読む

関連記事

共著者、ジャーナル、引用グラフによってこの研究に関連する記事。

並び替え
Same author

Coordinated chromosome motion emerges from mechanical coupling mediated by the physical spindle environment.

Molecular biology of the cell·2026
Same author

The Role of Transient Crosslinks in the Chromatin Search Response to DNA Damage.

International journal of molecular sciences·2025
Same author

Different relative scalings between transient forces and thermal fluctuations tune regimes of dynamic clustering.

Physical review. E·2025
Same author

The centromere bottlebrush requires a multi-microtubule attachment.

Molecular biology of the cell·2025
Same author

Centromeres are stress-induced fragile sites.

Current biology : CB·2025
Same author

Closing the loops: chromatin loop dynamics after DNA damage.

Nucleus (Austin, Tex.)·2024

関連する実験動画

Updated: Jun 16, 2026

Live Cell Imaging of Chromosome Segregation During Mitosis
06:39

Live Cell Imaging of Chromosome Segregation During Mitosis

Published on: March 14, 2018

染色体分離装置の構築に向けて

Kerry Bloom1, Ajit Joglekar

  • 1Department of Biology, 622 Fordham Hall, CB3280, University of North Carolina at Chapel Hill, North Carolina 27599, USA. kerry_bloom@unc.edu

Nature
|January 30, 2010
PubMed
まとめ

すべての生物は,細胞分裂の間にDNAをパッケージ化し分離する必要があります. これらの複雑なゲノム包装と分離機構の理解は,種によって大きく異なるため,極めて重要です.

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
  • 細胞生物学 細胞生物学

背景:

  • 細胞分裂には,大量のDNAの正確な複製,包装,分離が必要です.
  • DNA複製のメカニズムは十分に理解されているが,ゲノム包装と分離のプロセスは不明である.
  • これらのプロセスは,細菌から人間まで,すべての生命にとって根本的なものです.

研究 の 目的:

  • 細胞分裂中のDNA包装と分離の複雑なメカニズムを探求する.
  • 異なる生物体におけるこれらのメカニズムの多様性を強調する.
  • ゲノム組織を理解するための進行中の研究を強調するために.

主な方法:

  • 保存されたメカニズムと変数メカニズムを特定するための比較ゲノミクス分析.
  • DNAとタンパク質の相互作用を研究するための分子生物学技術.
  • 細胞イメージングは,分裂中のゲノム組織を視覚化します.

主要な成果:

  • 生物がDNAの包装と分離のために使用する多様な戦略を特定した.
  • ゲノム組織に関与する主要なタンパク質ファミリーを強調した.
  • 密接に関連した種間でもメカニズムの有意な違いが示されています.

さらに関連する動画

Use of Time-Lapse Microscopy and Stage-Specific Nuclear Depletion of Proteins to Study Meiosis in S. cerevisiae
07:48

Use of Time-Lapse Microscopy and Stage-Specific Nuclear Depletion of Proteins to Study Meiosis in S. cerevisiae

Published on: October 11, 2022

関連する実験動画

Last Updated: Jun 16, 2026

Live Cell Imaging of Chromosome Segregation During Mitosis
06:39

Live Cell Imaging of Chromosome Segregation During Mitosis

Published on: March 14, 2018

Use of Time-Lapse Microscopy and Stage-Specific Nuclear Depletion of Proteins to Study Meiosis in S. cerevisiae
07:48

Use of Time-Lapse Microscopy and Stage-Specific Nuclear Depletion of Proteins to Study Meiosis in S. cerevisiae

Published on: October 11, 2022

結論:

  • ゲノム包装と分離は,細胞分裂に不可欠な複雑で高度に変動するプロセスです.
  • 関連する多様な分子機構を完全に解明するためにさらなる研究が必要である.
  • これらのメカニズムを理解することは,発達生物学から疾患研究に至るまで,様々な分野において極めて重要です.