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Chromatin Immunoprecipitation (ChIP) Protocol for Low-abundance Embryonic Samples
Published on: August 29, 2017
Deep sequencing of chicken microRNAs
Joan Burnside1, Ming Ouyang, Amy Anderson
1Department of Animal and Food Sciences, Delaware Biotechnology Institute, University of Delaware, Newark, Delaware 19711, USA. joan@udel.edu
Deep sequencing identified novel chicken microRNAs and found that Marek's disease virus infection does not significantly alter microRNA expression profiles in chicken embryo fibroblasts.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Deep sequencing technologies accelerate microRNA discovery.
- This study focuses on chicken microRNAs (miRNAs) and their expression in chicken embryo fibroblasts (CEFs).
- Comparison of miRNAs in CEFs infected with Marek's disease virus (MDV) versus uninfected CEFs.
Purpose of the Study:
- Identify chicken microRNAs using deep sequencing.
- Compare miRNA profiles in MDV-infected and uninfected CEFs.
- Investigate the role of miRNAs in MDV-induced tumorigenesis.
Main Methods:
- Applied deep sequencing technology to analyze small RNA populations.
- Mapped high-quality reads to the chicken genome.
- Compared miRNA expression profiles between infected and uninfected CEFs.
Main Results:
- Obtained 125,463 high-quality reads matching the chicken genome.
- Identified numerous known and potential novel chicken microRNAs.
- MDV infection did not significantly alter the overall miRNA expression profile.
- Certain miRNAs (e.g., let-7, miR-199a-1, 26a) showed lower expression in MDV-induced tumors.
Conclusions:
- Deep sequencing is effective for small RNA discovery, independent of comparative sequence analysis.
- Confirmed expression of known chicken miRNAs and identified novel miRNA candidates.
- Suggests a potential role for specific miRNAs in MDV-related tumorigenesis.
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