Detection of differential DNA methylation under stress conditions using bisulfite sequence analysis

Ibtisam Al Harrasi, Rashid Al-Yahyai, Mahmoud W. Yaish

Research output: Chapter in Book/Report/Conference proceedingChapter

3 Citations (Scopus)

Abstract

DNA methylation is the most important epigenetic change affecting gene expression in plants grown under normal as well as under stress conditions. Therefore, researchers study differential DNA methylation under distinct environmental conditions and their relationship with transcriptome abundance. Up to date, more than 25 methods and techniques are available to detect DNA methylation based on different principles. Bisulfite sequencing method is considered as a gold standard since it is able to distinguish 5-methylcytosine from cytosine using the bisulfite treatment. Therefore, it is useful for qualitative and semiquantitative measurement of DNA methylation. However, the reliability of data obtaining from this technique is mainly depending on the efficiency of bisulfite conversion and number of sequencing clones representing the target-converted sequence. Therefore, it is labor intensive and time-consuming. Revolution of next generation DNA sequencing (NGS) has allowed researches to combine conventional bisulfite sequencing methods with high-throughput Illumina sequencing in a technique called whole genome bisulfite sequencing (WGBS). This technique allows a single nucleotide resolution of 5-methylcytosine on a genome scale. WGBS technique workflow involves DNA fragmentation, processing through end blunting, terminal A(s) addition at 3′ end and adaptor ligation, bisulfite treatment, PCR amplification, sequencing libraries and assembling, and finally alignment with the reference genome and data analysis. Despite the fact that WGBS is more reliable than the conventional clone-based bisulfite sequencing, it is costly, requires large amount of DNA and its output data is not easily handled.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages121-137
Number of pages17
Volume1631
DOIs
Publication statusPublished - 2017

Publication series

NameMethods in Molecular Biology
Volume1631
ISSN (Print)1064-3745

Fingerprint

DNA Methylation
Sequence Analysis
Genome
5-Methylcytosine
Clone Cells
hydrogen sulfite
Workflow
Cytosine
DNA Fragmentation
DNA Sequence Analysis
Transcriptome
Epigenomics
Ligation
Nucleotides
Research Personnel
Gene Expression
Polymerase Chain Reaction
DNA
Research

Keywords

  • Bisulfite
  • Cytosine
  • DNA methylation
  • Illumina
  • Methylcytosine
  • WGBS

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

Cite this

Al Harrasi, I., Al-Yahyai, R., & Yaish, M. W. (2017). Detection of differential DNA methylation under stress conditions using bisulfite sequence analysis. In Methods in Molecular Biology (Vol. 1631, pp. 121-137). (Methods in Molecular Biology; Vol. 1631). Humana Press Inc.. https://doi.org/10.1007/978-1-4939-7136-7_7

Detection of differential DNA methylation under stress conditions using bisulfite sequence analysis. / Al Harrasi, Ibtisam; Al-Yahyai, Rashid; Yaish, Mahmoud W.

Methods in Molecular Biology. Vol. 1631 Humana Press Inc., 2017. p. 121-137 (Methods in Molecular Biology; Vol. 1631).

Research output: Chapter in Book/Report/Conference proceedingChapter

Al Harrasi, I, Al-Yahyai, R & Yaish, MW 2017, Detection of differential DNA methylation under stress conditions using bisulfite sequence analysis. in Methods in Molecular Biology. vol. 1631, Methods in Molecular Biology, vol. 1631, Humana Press Inc., pp. 121-137. https://doi.org/10.1007/978-1-4939-7136-7_7
Al Harrasi I, Al-Yahyai R, Yaish MW. Detection of differential DNA methylation under stress conditions using bisulfite sequence analysis. In Methods in Molecular Biology. Vol. 1631. Humana Press Inc. 2017. p. 121-137. (Methods in Molecular Biology). https://doi.org/10.1007/978-1-4939-7136-7_7
Al Harrasi, Ibtisam ; Al-Yahyai, Rashid ; Yaish, Mahmoud W. / Detection of differential DNA methylation under stress conditions using bisulfite sequence analysis. Methods in Molecular Biology. Vol. 1631 Humana Press Inc., 2017. pp. 121-137 (Methods in Molecular Biology).
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