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Related Concept Videos

Circadian Rhythms and Gene Regulation02:19

Circadian Rhythms and Gene Regulation

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 years,...
Circadian Rhythms and Gene Regulation02:19

Circadian Rhythms and Gene Regulation

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 years,...
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The circadian—or biological—clock is an intrinsic, timekeeping, molecular mechanism that allows plants to coordinate physiological activities over 24-hour cycles called circadian rhythms. Photoperiodism is a collective term for the biological responses of plants to variations in the relative lengths of dark and light periods. The period of light-exposure is called the photoperiod.
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Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
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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

Weakly circadian cells improve resynchrony.

Alexis B Webb1, Stephanie R Taylor, Kurt A Thoroughman

  • 1Department of Biology, Washington University, St. Louis, Missouri, United States of America.

Plos Computational Biology
|December 5, 2012
PubMed
Summary

Neural network location significantly impacts circadian rhythm synchronization. Even weak oscillators can synchronize effectively when positioned at highly connected nodes within the suprachiasmatic nuclei (SCN) network.

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Area of Science:

  • Chronobiology
  • Neuroscience
  • Systems Biology

Background:

  • Mammalian suprachiasmatic nuclei (SCN) neurons generate near 24-hour rhythms, but exhibit diverse oscillatory phenotypes when isolated.
  • The functional implications of this cellular variability within the SCN network remain unclear.

Purpose of the Study:

  • To investigate how a neuron's location within the SCN network influences its resynchronization and the overall population synchrony.
  • To determine if intrinsic cellular properties and network connectivity interact to shape circadian rhythm dynamics.

Main Methods:

  • Utilized a deterministic, mechanistic model of circadian oscillators to independently control cell-intrinsic parameters (period, amplitude) and network connectivity.
  • Simulated a range of oscillatory phenotypes by altering model parameters, mirroring biological cell variability.
  • Employed a phase-amplitude model to independently verify findings on synchronization.

Main Results:

  • Small variations in cell-intrinsic parameters generated diverse oscillatory phenotypes, including differences in period, amplitude, and cycling ability.
  • Weaker oscillators demonstrated greater phase adjustability compared to stronger oscillators.
  • Network synchronization improved when weaker oscillators occupied highly connected network nodes.

Conclusions:

  • Intrinsic cellular properties significantly influence individual neuron's oscillatory capacity.
  • The strategic placement of weaker oscillators within highly connected network regions is crucial for enhancing population-level synchronization in the SCN.