For each citation that was shared on social media (LinkedIn, Facebook, or Twitter) with the “@GenScript” tag, the author will be rewarded with a $10 Amazon gift card or 2,000 GS points.

Comparative analysis of maize root sRNA transcriptome unveils the regulatory roles of miRNAs in submergence stress response mechanism

Environmental and Experimental Botany. 2020; 
IkbalAzaharaSupriyaGhoshaAyanAdhikariaSinchanAdhikariaDoyelRoyaArun K.ShawbKashmirSinghcZahedHossaina
Products/Services Used Details Operation
Gene Synthesis Total RNA extraction and first strand cDNA synthesis were performed following same method described earlier (Ghosh et al., 2016). All the miRNA target gene sequences used for primer designing were taken from our dataset whose transcript sequences were downloaded from psRNA Target (http://plantgrn.noble.org/psRNATarget/). The primers for quantitative real-time PCR (qRT-PCR) analysis were designed using the GenScript software (https://www.genscript.com/ssl-bin/app/primer). All the qRT-PCR reactions were performed using three biological and two technical replicates. The sequences of primer pairs used for the target genes are presented in Table S2b. Get A Quote

Abstract

Oxygen limitation under submerged condition induces hypoxic stress and causes a metabolic shift from aerobic respiration to anaerobic fermentation. Submergence stress often limits plant growth and causes substantial yield loss. The present small RNA (sRNA) transcriptome study aims to identify and characterise submergence responsive miRNAs to delineate the response mechanisms of maize seedlings to complete submergence. In this study, we constructed two sRNA libraries from control and submerged maize roots. Deep sequencing revealed 524 known (conserved and non-conserved) and 48 novel miRNAs from two libraries. Out of 188 commonly expressed known miRNAs, 45 miRNAs were found to be differentially expressed (43 down... More

Keywords