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Biology
Metodo per l'etichettatura di trascrizioni in cellule individuali Escherichia coli per s...
Metodo per l'etichettatura di trascrizioni in cellule individuali Escherichia coli per s...
JoVE Journal
Biology
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JoVE Journal Biology
Method for Labeling Transcripts in Individual Escherichia coli Cells for Single-molecule Fluorescence In Situ Hybridization Experiments

Metodo per l'etichettatura di trascrizioni in cellule individuali Escherichia coli per singola molecola di fluorescenza In Situ gli esperimenti di ibridazione

Full Text
8,806 Views
07:51 min
December 21, 2017

DOI: 10.3791/56600-v

Rinat Arbel-Goren1, Yonatan Shapira1, Joel Stavans1

1Department of Physics of Complex Systems,Weizmann Institute of Science

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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 manuscript describes a method for labeling individual messenger RNA (mRNA) transcripts with fluorescently-labeled DNA probes for use in single-molecule fluorescence in situ hybridization (smFISH) experiments in E. coli. This technique allows for the simultaneous detection, localization, and quantification of single mRNA molecules in fixed individual cells.

Key Study Components

Area of Science

  • Neuroscience
  • Systems Biology
  • Cell Biology

Background

  • Single-molecule fluorescence in situ hybridization (smFISH) is a powerful visualization method.
  • This method enables the study of transcriptional processes at the single-cell level.
  • Understanding mRNA localization and quantification is crucial for systems biology.
  • E. coli serves as a model organism for these experiments.

Purpose of Study

  • To label individual mRNA transcripts in E. coli.
  • To visualize mRNA localization using fluorescently labeled DNA probes.
  • To enhance understanding of transcriptional variability among cells.

Methods Used

  • Grow E. coli MG1655 in LB medium overnight.
  • Dilute the overnight culture in fresh medium.
  • Measure optical density to ensure proper growth conditions.
  • Apply fluorescently labeled DNA probes for smFISH analysis.

Main Results

  • Successful labeling of individual mRNA transcripts.
  • Visualization of mRNA localization within fixed cells.
  • Quantification of transcriptional processes at the single-molecule level.
  • Insights into cell-to-cell variability in transcript expression.

Conclusions

  • The method provides a robust approach for studying mRNA dynamics.
  • It contributes valuable information to the field of systems biology.
  • This technique can be applied to various research questions regarding gene expression.

Frequently Asked Questions

What is smFISH?
smFISH is a technique used to visualize and quantify individual mRNA molecules in cells.
Why use E. coli for this study?
E. coli is a well-established model organism that allows for controlled experiments in molecular biology.
What are the advantages of using fluorescently labeled DNA probes?
Fluorescently labeled DNA probes enable precise localization and quantification of mRNA transcripts.
How does this method contribute to systems biology?
It provides insights into transcriptional variability and mRNA dynamics at the single-cell level.
What is the significance of measuring optical density?
Measuring optical density ensures that the bacterial culture is at the appropriate growth phase for experiments.
Can this method be applied to other organisms?
Yes, while this study focuses on E. coli, the method can be adapted for use in other cell types.

Questo manoscritto descrive un metodo per l'etichettatura individuale RNA messaggero (mRNA) trascrizioni con sonde di DNA fluorescente etichettati, per l'uso in singola molecola fluorescenza in situ (smFISH) gli esperimenti di ibridazione in Escherichia coli. smFISH è un metodo di visualizzazione che permette la rilevazione simultanea, la localizzazione e quantificazione delle singole molecole di mRNA in singole celle fisse.

L'obiettivo generale di questo protocollo è quello di marcare singoli trascritti in E.Coli per sonde di DNA marcate in fluorescenza per la visualizzazione in esperimenti FiSH a singola molecola. Questo metodo può aiutare a rispondere a domande chiave nel campo della biologia dei sistemi, come la caratterizzazione delle trascrizioni della capacità cellula-cellula del campo di interesse. Così come i trascritti di localizzazione della parete cellulare.

Il vantaggio principale di questa tecnica è che fornisce una quantità di informazioni sulle statistiche dei processi trascrizionali. Per iniziare il protocollo, coltivare E.Coli MG1655 in terreno LB durante la notte in un agitatore orbitale, a 260 giri/min e 37 gradi Celsius. Il giorno successivo, diluire la coltura notturna a una temperatura compresa tra 1 e 100 in terreno fresco e misurarne la densità ottica in uno spettrofotometro, fino a un valore compreso tra 0,2 e 0,4.

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