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JoVE Journal
Neuroscience
In Vivo Suivi de l’Expression génique horloge circadienne dans le noyau suprachiasmatiqu...
In Vivo Suivi de l’Expression génique horloge circadienne dans le noyau suprachiasmatiqu...
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
In Vivo Monitoring of Circadian Clock Gene Expression in the Mouse Suprachiasmatic Nucleus Using Fluorescence Reporters

In Vivo Suivi de l’Expression génique horloge circadienne dans le noyau suprachiasmatique de souris à l’aide de Reporters de Fluorescence

Full Text
8,871 Views
07:44 min
July 4, 2018

DOI: 10.3791/56765-v

Long Mei1,2, Cheng Zhan2, Eric Erquan Zhang2

1PTN Joint Graduate Program, School of Life Sciences,Peking University, 2National Institute of Biological Sciences, Beijing

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This study presents a fluorescence-based technology for long-term monitoring of circadian clock gene transcription in the suprachiasmatic nucleus (SCN) of freely moving mice. The method is capable of real-time measurements at high temporal resolution and operates in both light-dark and dark-dark conditions, which is crucial for circadian research.

Key Study Components

Area of Science

  • Neuroscience
  • Circadian Rhythms
  • Gene Expression Monitoring

Background

  • The suprachiasmatic nucleus (SCN) is responsible for regulating circadian rhythms in mammals.
  • Monitoring gene expression in real-time is crucial for understanding circadian biology.
  • Existing methods may not allow for effective measurement during varying light conditions.
  • This technology aims to address those limitations by enabling precise monitoring under both light and dark conditions.

Purpose of Study

  • To develop a method for real-time tracking of circadian clock gene expression in freely moving mice.
  • To ensure effective monitoring across different lighting conditions.
  • To enhance the understanding of SCN functioning and circadian rhythm dynamics.

Methods Used

  • The study utilized a fluorescence-based monitoring system integrated into an optical fiber setup.
  • The biological model involved adult mice, specifically focusing on the SCN.
  • No multiomics workflows were mentioned.
  • Key steps include the surgical injection of recombinant AAV and positioning the fiber for monitoring.
  • Measurements of fluorescence were taken at specified intervals for data collection and analysis.

Main Results

  • A clear Venus expression was observed in the SCN after viral vector injection.
  • The study reported background fluorescence levels in control mice, establishing a basis for evaluating gene expression.
  • Circadian rhythm analysis demonstrated rhythmic gene expression in both light-dark and dark-dark conditions.
  • The findings validate the method for studying circadian clock dynamics in live animals.

Conclusions

  • This technique demonstrates an effective approach to monitor real-time gene expression in circadian studies.
  • The method facilitates further exploration of neuronal mechanisms related to circadian rhythms.
  • Understanding SCN dynamics can lead to insights into sleep disorders and related conditions.

Frequently Asked Questions

What are the advantages of this monitoring technique?
This fluorescence-based method provides real-time insights into gene expression in freely moving mice, allowing for unprecedented observation of circadian rhythms in both light and dark conditions.
How is the AAV injected into the SCN?
The injection is performed using a microsyringe after anesthetizing the mouse and preparing the surgical site, ensuring precise delivery of the viral vector.
What type of data is obtained using this method?
Data includes real-time fluorescence measurements, allowing for analysis of circadian gene expression patterns in the SCN over time.
Can this method be adapted for other light conditions?
Yes, the technique is designed to operate effectively under various light conditions, making it suitable for comprehensive circadian studies.
What limitations should be considered in this study?
The main limitations include the need for precise surgical placement of the optic fiber and potential variations in fluorescence signal based on individual animal responses.
What insights can this study provide for understanding circadian rhythms?
It enhances understanding of the cellular mechanisms driving circadian rhythms and how gene expression changes in different environmental conditions may influence behavior.

Cette technologie nouvellement développée basés sur la fluorescence permet une surveillance à long terme de la transcription des gènes de l’horloge circadienne dans le noyau suprachiasmatique (SCN) de se déplaçant librement les souris en temps réel et à une haute résolution temporelle.

Cette méthode permet de surveiller l’expression des gènes de l’horloge circadienne en temps réel et à haute résolution temporelle chez des souris se déplaçant librement. Le principal avantage de cette technique est qu’elle fonctionne à la fois dans des conditions claire-obscurité et sombre-obscurité, qui sont d’une importance cruciale pour l’étude de l’horloge circadienne. À l’aide d’un couteau à fibre optique, coupez une fibre de 17 millimètres de longueur.

S’assurer que chaque côté de la fibre optique est lisse. Insérez la fibre optique dans la virole en céramique et fixez la fibre optique à une virole en céramique avec du peroxyde de méthyléthylcétone. S’assurer que les surfaces de la fibre optique et de la virole en céramique sont affleurantes.

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