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Review
. 2022 Oct 31:219:1261-1271.
doi: 10.1016/j.ijbiomac.2022.08.182. Epub 2022 Aug 31.

A review on CRISPR/Cas-based epigenetic regulation in plants

Phanikanth Jogam  1 , Dulam Sandhya  2 , Anshu Alok  3 , Venkataiah Peddaboina  4 , Venkateswar Rao Allini  2 , Baohong Zhang  5
Affiliations
Review

A review on CRISPR/Cas-based epigenetic regulation in plants

Phanikanth Jogam et al. Int J Biol Macromol. .

Abstract

Epigenetic changes are the heritable modifications in genes without altering DNA sequences. The epigenetic changes occur in the plant genomes to regulate gene expression patterns, which were used to regulate different biological processes, including coping various environmental stresses. These changes, including DNA methylation, non-coding RNA regulation, and histone modification, play a vital role in the transcription and translation processes to regulate gene expression. Gene engineering for the development of stress-tolerant crops via the DNA methylation pathway initially needs a proper selection of genes and its promoter. Manipulating epigenetics requires genetic engineering tools such as Zinc finger nucleases (ZFN), transcription activator-like effector nucleases (TALENs), and clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein (Cas). However, CRISPR/Cas9 mediated epigenetic editing refers to transcriptional reprogramming at the targeted sites using epigenetic enzymes fused with decatalytical Cas9 (dCas9). This review focused on the different epigenetic mechanisms in plants and their potential contribution to developing epigenetic tools. The dCas9 endonuclease tethered with transcriptional repressor or activator domain leads to CRISPR inhibitor (CRISPRi) or activator (CRISPRa) for regulating gene expression. The dCas9 has been successfully fused with other various effector domains for constructing epigenetic tools, including the DNA methyltransferase 3A (DNMT3A), or the DNA demethylase TET. Multiple efforts have been made to improve epigenome editing in plants. Initially, incorporating SunTag into the dCas9-EpiEffector complex was used as an epigenetic tool; demethylation of target loci with dCas9-SunTag-TET1 futher increased its efficiency. Additionally, SunTag could also be fused with the dCas9-DNMT3A complex to augment CpG methylation at a targeted loci.

Keywords: DNA methylation; Deactivated Cas9 (dCas9); Histone modification; Non-coding RNA.

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Conflict of interest statement

Declaration of competing interest The authors declare no conflict of interest.

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