Abstract
As a functional compartment, the nuclear periphery plays critical roles in regulating the spatial organization of chromatin in the nuclei and gene expression. Generally, the nuclear periphery is a transcriptionally repressed compartment enriched for silenced chromatin. Methods of investigating chromatin positioning at the nuclear periphery in plants will substantially advance our understanding of transcriptional regulation in this subnuclear compartment. Here, we describe a detailed RE-ChIP-seq (restriction enzyme-mediated ChIP-sequencing) protocol, which combines restriction enzyme-mediated chromatin fragmentation, chromatin immunoprecipitation, and next generation sequencing approaches, to identify chromatin that positioned at the nuclear periphery in Arabidopsis. Different from a regular chromatin immunoprecipitation method, RE-ChIP allows specific enrichment of chromatin located near the protein of interest regardless of having direct interactions. In principle, this approach is applicable to identify target chromatin of transcriptional coregulators, which often do not directly bind DNA.
Key words
- RE-ChIP
- Nuclear periphery
- Chromatin positioning
This is a preview of subscription content, access via your institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsReferences
Gibcus JH, Dekker J (2013) The hierarchy of the 3D genome. Mol Cell 49:773–782
Harr JC, Gonzalez-Sandoval A, Gasser SM (2016) Histones and histone modifications in perinuclear chromatin anchoring: from yeast to man. EMBO Rep 17:139–155
Pawar V, Poulet A, Detourne G, Tatout C, Vanrobays E, Evans DE, Graumann K (2016) A novel family of plant nuclear envelope-associated proteins. J Exp Bot 67:5699–5710
Poulet A, Duc C, Voisin M, Desset S, Tutois S, Vanrobays E, Benoit M, Evans DE, Probst AV, Tatout C (2017) The LINC complex contributes to heterochromatin organisation and transcriptional gene silencing in plants. J Cell Sci 130:590–601
Kubben N, Adriaens M, Meuleman W, Voncken JW, van Steensel B, Misteli T (2012) Mapping of lamin A- and progerin-interacting genome regions. Chromosoma 121:447–464
Lund E, Oldenburg AR, Delbarre E, Freberg CT, Duband-Goulet I, Eskeland R, Buendia B, Collas P (2013) Lamin A/C-promoter interactions specify chromatin state-dependent transcription outcomes. Genome Res 23:1580–1589
Sadaie M, Salama R, Carroll T, Tomimatsu K, Chandra T, Young AR, Narita M, Perez-Mancera PA, Bennett DC, Chong H, Kimura H, Narita M (2013) Redistribution of the Lamin B1 genomic binding profile affects rearrangement of heterochromatic domains and SAHF formation during senescence. Genes Dev 27:1800–1808
Shah PP, Donahue G, Otte GL, Capell BC, Nelson DM, Cao K, Aggarwala V, Cruickshanks HA, Rai TS, McBryan T, Gregory BD, Adams PD, Berger SL (2013) Lamin B1 depletion in senescent cells triggers large-scale changes in gene expression and the chromatin landscape. Genes Dev 27:1787–1799
Vogel MJ, Peric-Hupkes D, van Steensel B (2007) Detection of in vivo protein-DNA interactions using DamID in mammalian cells. Nat Protoc 2:1467–1478
van Steensel B, Henikoff S (2000) Identification of in vivo DNA targets of chromatin proteins using tethered dam methyltransferase. Nat Biotechnol 18:424–428
Kind J, Pagie L, Ortabozkoyun H, Boyle S, de Vries SS, Janssen H, Amendola M, Nolen LD, Bickmore WA, van Steensel B (2013) Single-cell dynamics of genome-nuclear lamina interactions. Cell 153:178–192
Ciska M, Moreno Diaz de la Espina S (2014) The intriguing plant nuclear lamina. Front Plant Sci 5:166
Parry G (2015) The plant nuclear envelope and regulation of gene expression. J Exp Bot 66:1673–1685
Bi X, Cheng Y, Hu B, Ma X, Wu R, Wang J, Liu C (2017) Non-random domain organization of the Arabidopsis genome at the nuclear periphery. Genome Res 27:1162
Boyd KE, Farnham PJ (1997) Myc versus USF: discrimination at the cad gene is determined by core promoter elements. Mol Cell Biol 17:2529–2537
Kang SH, Vieira K, Bungert J (2002) Combining chromatin immunoprecipitation and DNA footprinting: a novel method to analyze protein-DNA interactions in vivo. Nucleic Acids Res 30:e44
Schuch R, Agelopoulos K, Neumann A, Brandt B, Burger H, Korsching E (2012) Site-specific chromatin immunoprecipitation: a selective method to individually analyze neighboring transcription factor binding sites in vivo. BMC Res Notes 5:109
Wang C, Liu C, Roqueiro D, Grimm D, Schwab R, Becker C, Lanz C, Weigel D (2015) Genome-wide analysis of local chromatin packing in Arabidopsis thaliana. Genome Res 25:246–256
Acknowledgment
This work was supported by Deutsche Forschungsgemeinschaft (LI 2862/1).
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2018 Springer Science+Business Media, LLC, part of Springer Nature
About this protocol
Cite this protocol
Bi, X., Liu, C. (2018). Genome-Wide Identification of Chromatin Domains Anchored at the Nuclear Periphery in Plants. In: Yamaguchi, N. (eds) Plant Transcription Factors. Methods in Molecular Biology, vol 1830. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-8657-6_23
Download citation
DOI: https://doi.org/10.1007/978-1-4939-8657-6_23
Published:
Publisher Name: Humana Press, New York, NY
Print ISBN: 978-1-4939-8656-9
Online ISBN: 978-1-4939-8657-6
eBook Packages: Springer Protocols