An improved restriction enzyme accessibility assay for analyzing changes in chromatin structure in samples of limited cell number

Yasuyuki Ohkawa, Chandrashekara Mallappa, Caroline S.Dacwag Vallaster, Anthony N. Imbalzano

Research output: Chapter in Book/Report/Conference proceedingChapter

6 Citations (Scopus)

Abstract

Studies investigating mechanisms that control gene regulation frequently examine the accessibility of specific DNA sequences to nuclease cleavage. In general, sequences that are sensitive to nuclease cleavage are considered to be in an "open" chromatin conformation that is associated with regulatory factor binding, while sequences resistant to nuclease cleavage are considered to be in a "closed" conformation commonly associated with chromatin that is neither poised for transcription nor being actively transcribed. Changes in nuclease accessibility at specific genomic sequences reflect changes in the local chromatin structure that can occur as a result of signaling cues in the extracellular environment. These changes in chromatin structure usually precede or are coincident with changes in gene expression patterns and are therefore a useful marker of regulatory events controlling transcription. We describe a method to perform restriction enzyme accessibility assays (REAA) that utilizes ligation-mediated polymerase chain reaction (LM-PCR) technology and that permits assessment of samples from any source containing as few as 1,000 cells. Use of this modified REAA protocol will enhance analysis of chromatin structural changes at specific DNA sequences of interest by making it possible to analyze samples where unrestricted amounts of sample are not readily available.

Original languageEnglish
Title of host publicationMyogenesis
Subtitle of host publicationMethods and Protocols
EditorsJoseph DiMario
Pages531-542
Number of pages12
DOIs
Publication statusPublished - Jan 2 2012

Publication series

NameMethods in Molecular Biology
Volume798
ISSN (Print)1064-3745

Fingerprint

Enzyme Assays
Chromatin
Cell Count
Biomedical Technology Assessment
Cues
Ligation
Gene Expression
Polymerase Chain Reaction
Genes

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics

Cite this

Ohkawa, Y., Mallappa, C., Vallaster, C. S. D., & Imbalzano, A. N. (2012). An improved restriction enzyme accessibility assay for analyzing changes in chromatin structure in samples of limited cell number. In J. DiMario (Ed.), Myogenesis: Methods and Protocols (pp. 531-542). (Methods in Molecular Biology; Vol. 798). https://doi.org/10.1007/978-1-61779-343-1_32

An improved restriction enzyme accessibility assay for analyzing changes in chromatin structure in samples of limited cell number. / Ohkawa, Yasuyuki; Mallappa, Chandrashekara; Vallaster, Caroline S.Dacwag; Imbalzano, Anthony N.

Myogenesis: Methods and Protocols. ed. / Joseph DiMario. 2012. p. 531-542 (Methods in Molecular Biology; Vol. 798).

Research output: Chapter in Book/Report/Conference proceedingChapter

Ohkawa, Y, Mallappa, C, Vallaster, CSD & Imbalzano, AN 2012, An improved restriction enzyme accessibility assay for analyzing changes in chromatin structure in samples of limited cell number. in J DiMario (ed.), Myogenesis: Methods and Protocols. Methods in Molecular Biology, vol. 798, pp. 531-542. https://doi.org/10.1007/978-1-61779-343-1_32
Ohkawa Y, Mallappa C, Vallaster CSD, Imbalzano AN. An improved restriction enzyme accessibility assay for analyzing changes in chromatin structure in samples of limited cell number. In DiMario J, editor, Myogenesis: Methods and Protocols. 2012. p. 531-542. (Methods in Molecular Biology). https://doi.org/10.1007/978-1-61779-343-1_32
Ohkawa, Yasuyuki ; Mallappa, Chandrashekara ; Vallaster, Caroline S.Dacwag ; Imbalzano, Anthony N. / An improved restriction enzyme accessibility assay for analyzing changes in chromatin structure in samples of limited cell number. Myogenesis: Methods and Protocols. editor / Joseph DiMario. 2012. pp. 531-542 (Methods in Molecular Biology).
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