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AtMBD4: A methylated DNA binding protein negatively regulates a subset of phosphate starvation genes.

Authors :
PARIDA, ADWAITA PRASAD
SHARMA, AMRAPALI
SHARMA, ARUN KUMAR
Source :
Journal of Biosciences; Mar2019, Vol. 44 Issue 1, p1-15, 15p, 3 Diagrams, 1 Chart, 4 Graphs
Publication Year :
2019

Abstract

DNA methylation is an important epigenetic modification that governs transcriptional regulation. The methylation mark is read by a special class of proteins called methyl-CpG-binding domain proteins. The role of DNA methylation has been found in X-chromosome inactivation, genomic imprinting, transposon silencing, and self-incompatibility. Recently, remodeling of global DNA methylation was demonstrated in Arabidopsis during low phosphate availability. The present study reports that AtMBD4 gene of Arabidopsis negatively regulates phosphate starvation. The T-DNA insertion mutation at the AtMBD4 locus exhibited altered root architecture as compared to wild-type plants. Using microarray hybridization and analysis, an increased transcript accumulation of 242 genes was observed in the mutant. Many of these genes were related to phosphate transporters and transcription factors, involved in phosphate starvation response. Comparison of data of atmbd4 mutant with publicly available microarray data of phosphate starvation response indicated the role of AtMBD4 protein in phosphate starvation response. Further, promoter analysis of up-regulated genes suggested that cis-regulatory elements like MBS, W-box, and B1BS are more prominent in the promoters of up-regulated genes. Upon performing a methylation-specific PCR, a decreased DNA methylation in the promoter regions of up-regulated genes was observed. The accumulation of anthocyanin and inorganic phosphate in the atmbd4 mutant was found to be higher than the wild-type plant. Altered root morphology, up-regulation of phosphate starvation-induced genes in atmbd4 mutant suggests that AtMBD4 negatively regulates the phosphate starvation response. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02505991
Volume :
44
Issue :
1
Database :
Complementary Index
Journal :
Journal of Biosciences
Publication Type :
Academic Journal
Accession number :
136699900
Full Text :
https://doi.org/10.1007/s12038-018-9843-5