Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Circadian Rhythms and Gene Regulation02:19

Circadian Rhythms and Gene Regulation

4.4K
The biological clock is involved in many aspects of regulating complex physiology in all animals. It was in 1935 when German zoologists, Hans Kalmus and Erwin Bünning, discovered the existence of circadian rhythm in Drosophila melanogaster. However, the internal molecular mechanisms behind the circadian clock remained a mystery until 1984, when Jeffrey C. Hall, Michael Rosbash, and Michael W. Young discovered the expression of the Per gene oscillating over a 24-hour cycle. In subsequent...
4.4K
The Cell Cycle Control System01:28

The Cell Cycle Control System

5.1K
The cell cycle regulation directs how a cell proceeds from one phase to the next and begins mitosis. The cell cycle control system includes intracellular regulatory molecules and external triggers. They provide "stop" or "advance" signals and operate at specific cell cycle stages termed checkpoints to ensure that a particular process is completed before the cell advances to the next phase.
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
5.1K
The Cell Cycle Control System02:11

The Cell Cycle Control System

13.7K
The cell cycle is an organized set of events that leads the cell to divide into two daughter cells, each containing chromosomes identical to the parent cell. It is the cell cycle that leads to the formation of an entire organism from a single-cell zygote. Besides, cell division also functions in the renewal or repair of tissues in adult multicellular eukaryotes. For example, in the bone marrow, the stem cells divide to form new blood cells. Although essential for several functions, cell...
13.7K
Molecular Factors Affecting Cell Division01:27

Molecular Factors Affecting Cell Division

3.7K
Several external and internal factors influence the initiation and inhibition of cell division. For instance, the death of nearby cells or the release of human growth hormone (hGH) promotes cell division. In contrast, lack of hGH or crowding of cells can inhibit cell division.
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
3.7K
Positive Regulator Molecules01:45

Positive Regulator Molecules

132.7K
To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
132.7K
Positive Regulator Molecules02:39

Positive Regulator Molecules

6.4K
Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
6.4K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Quenching of the π0p_{3/2}-π0p_{1/2} Spin-Orbit Splitting in ^{20}O and the Effect of the Tensor Force.

Physical review letters·2026
Same author

Simultaneous NOD1 and NOD2 Deletion in Hematopoietic Stem and Progenitor cells Promotes Long-Term Donor Chimerism.

Transplantation and cellular therapy·2026
Same author

Unveiling the potential of copper-61 vs. gallium-68 for SSTR PET imaging.

European journal of nuclear medicine and molecular imaging·2025
Same author

Magicity versus Superfluidity around ^{28}O viewed from the Study of ^{30}F.

Physical review letters·2024
Same author

High-Precision Spectroscopy of ^{20}O Benchmarking Ab Initio Calculations in Light Nuclei.

Physical review letters·2024
Same author

Publisher Correction: First observation of <sup>28</sup>O.

Nature·2023

Related Experiment Video

Updated: Dec 18, 2025

Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures
06:53

Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures

Published on: November 11, 2016

8.7K

Cell cycle period control through modulation of clock inputs.

S Almeida1, M Chaves2, F Delaunay3

  • 1Inria, iBV, UniversitĂ© CĂ´te d'Azur, Sophia Antipolis, France.

Journal of Bioinformatics and Computational Biology
|June 20, 2020
PubMed
Summary
This summary is machine-generated.

This study demonstrates slowing the mammalian cell cycle by coupling it with the cellular clock. Clock inputs effectively modulate cell cycle duration, offering potential therapeutic strategies targeting cell proliferation.

Keywords:
Modelingcell cyclecircadian clockperiod controlsynchronization

More Related Videos

In Vitro Bioluminescence Assay to Characterize Circadian Rhythm in Mammary Epithelial Cells
11:56

In Vitro Bioluminescence Assay to Characterize Circadian Rhythm in Mammary Epithelial Cells

Published on: September 28, 2017

10.2K
Monitoring Cell-autonomous Circadian Clock Rhythms of Gene Expression Using Luciferase Bioluminescence Reporters
10:38

Monitoring Cell-autonomous Circadian Clock Rhythms of Gene Expression Using Luciferase Bioluminescence Reporters

Published on: September 27, 2012

23.0K

Related Experiment Videos

Last Updated: Dec 18, 2025

Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures
06:53

Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures

Published on: November 11, 2016

8.7K
In Vitro Bioluminescence Assay to Characterize Circadian Rhythm in Mammary Epithelial Cells
11:56

In Vitro Bioluminescence Assay to Characterize Circadian Rhythm in Mammary Epithelial Cells

Published on: September 28, 2017

10.2K
Monitoring Cell-autonomous Circadian Clock Rhythms of Gene Expression Using Luciferase Bioluminescence Reporters
10:38

Monitoring Cell-autonomous Circadian Clock Rhythms of Gene Expression Using Luciferase Bioluminescence Reporters

Published on: September 27, 2012

23.0K

Area of Science:

  • * Molecular and Systems Biology
  • * Chronobiology
  • * Cell Cycle Regulation

Background:

  • * The mammalian cell cycle and cellular clock are interconnected through molecular mechanisms.
  • * The CLOCK:BMAL1 complex regulates the *wee1* gene, influencing the cell cycle's mitosis promoting factor (MPF).
  • * Understanding these interactions is crucial for controlling cell proliferation.

Purpose of the Study:

  • * To investigate period control of the mammalian cell cycle by coupling it with the cellular clock.
  • * To explore methods for slowing the cell cycle using clock-based inputs.
  • * To propose and analyze a model of a Growth Factor (GF)-responsive clock.

Main Methods:

  • * Utilized mathematical models of cellular clock and cell cycle oscillators.
  • * Focused on unidirectional coupling dynamics between the clock and cell cycle.
  • * Investigated synchronization dynamics and period ratios (e.g., 1:1, 3:2).

Main Results:

  • * Demonstrated successful period control of the cell cycle via clock inputs.
  • * Observed various rational period ratios between the clock and cell cycle.
  • * Identified clock modulation protocols capable of slowing the cell cycle.

Conclusions:

  • * Clock inputs can effectively slow down the mammalian cell cycle.
  • * The proposed GF-responsive clock model offers new insights.
  • * Developed protocols show potential for therapeutic applications using existing drugs.