Evidence map›Paper›PMID 41051666›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Single-Base Resolution DNA Methylation Analysis Through Targeted Locus-Specific Bisulfite Sequencing in Plants.

Kirti Pandey, Gaurav Zinta

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Kirti PandeyIntegrative Plant AdaptOmics Lab (iPAL), Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology (IHBT), Palampur, Himachal Pradesh, India.
Gaurav ZintaIntegrative Plant AdaptOmics Lab (iPAL), Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology (IHBT), Palampur, Himachal Pradesh, India. gauravzinta@ihbt.res.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation, a key epigenetic modification, influences gene expression, represses transposable elements, and mediates plant responses to environmental stress by adding methyl groups to cytosine residues (5mC) in CG, CHG, and CHH contexts. There are several methods for locus-specific DNA methylation analysis, each with its own advantages and limitations, including bisulfite sequencing PCR (BSP), methylation-specific PCR (MSP), bisulfite pyrosequencing, epityper, methylation-sensitive restriction enzyme (MSRE)-based approaches such as MSRE-Southern blot and MSRE-PCR, methylation-dependent restriction enzyme methods like McrBC, and Affinity Enrichment-based techniques. Here, we present a detailed protocol for locus-specific DNA methylation analysis, highlighting sodium bisulfite sequencing as the gold standard due to its single-base resolution, simplicity, and high accuracy. This protocol utilizes the EZ DNA Methylation-Gold™ Kit for bisulfite conversion, which selectively deaminates unmethylated cytosines to uracil while preserving methylated cytosines. The procedure involves treatment with the CT conversion reagent, followed by thermal cycling and purification using Zymo-Spin™ IC columns. To ensure specific and unbiased amplification of bisulfite-converted DNA, primers are carefully designed using tools such as MethPrimer and BiSearch. Following bisulfite conversion and PCR amplification of the target region, the amplified products are cloned into a binary vector and subjected to Sanger sequencing, enabling single-base resolution analysis of DNA methylation patterns. This approach allows for precise mapping of DNA methylation at promoters, enhancers, and transposable elements, providing valuable insights into gene regulation and phenotypic variation. Locus-specific DNA methylation analysis in plants has wide-ranging applications, including the study of epigenetic responses to stress, transgenerational inheritance, and crop improvement.

Indexed as

DNA MethylationDNA, PlantGenetic LociPlantsSequence Analysis, DNASulfitesEpigenesis, GeneticPolymerase Chain ReactionDNA, Planthydrogen sulfiteSulfitesBisulfite sequencingDNA methylationEpigenetic modificationGene regulationMethylation analysis

Identifiers

PMID41051666

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