Gene Expression Nebulas
A data portal of transcriptomic profiles across multiple species

Gene Expression Nebulas

A data portal of transcriptome profiles across multiple species

PRJNA436566: Dynamics and functional interplay of histone lysine butyrylation, crotonylation, and acetylation in rice under starvation and submergence

Source: NCBI / GSE111308
Submission Date: Mar 01 2018
Release Date: Sep 08 2018
Update Date: Sep 09 2018

Summary: In this work, we detected lysinebutyrylation (Kbu) and crotonylation(Kcr) sites in rice histone proteins by mass spectrometry, and found both similar and specific acylation patterns compared with that in mammalian cells. Comparative analysis of genome-wide histone Kbu, Kcr, and H3K9ac in combination of RNA-sequencing revealed that a large number of rice genes are marked by both Kbu and Kcr, most of which overlap with H3K9ac and are active genes. Under starvation and submergence, Kbu andKcr appeared to be less dynamic than H3K9ac and the three marks displayed changes in different sets of genes. Kbu and Kcr seemed to have a function to poise stress-induced gene activation. The results suggest that histone Kbu and Kcr provide a platform for histone acetylation during gene activation and that the proportional mixture of distinct histone lysine acylations which are regulated by environmental cues and has functionally consequence in chromatin modification and gene expression in plants.

Overall Design: RNA-seq and H3K9ac, Kbu, and Kcr ChIP-seq of rice seedlings under normal conditions and starvation and submergence treatments; RNA-seq and H3K9ac ChIP-seq of rice leaf in 4 diurnal times.

GEN Datasets:
Development Stage:
Growth Protocol: Rice seeds were germinated and grown on the hormone-free, half-strength Murashige & Skoog (MS) medium under 16/8 hrs light/dark at 30/25°C.
Treatment Protocol: For starvation treatment, seedlings were moved into dark culture at 10 DAG 6:00pm and treated for 48 hours. For submergence treatment, seedlings were submerged in distilled water at 12DAG 12:00am and treated for 6 hours. Seedling leaves from each group were harvested at 12DAG 6:00pm for chromatin and total RNA extraction.
Extract Protocol: RNA samples were isolated using TRIzol reagent (Invitrogen).
Library Construction Protocol: The RNA-seq libraries were prepared using the Illumina TruSeq RNA Sample Preparation Kit and sequenced on Illumina HiSeq 2000 with PE150 method.
Molecule Type: poly(A)+ RNA
Library Source:
Library Layout: PAIRED; SINGLE
Library Strand: -; Forward; Reverse
Platform: ILLUMINA
Instrument Model: Illumina HiSeq 2000
Strand-Specific: Unspecific; Specific
Dynamics and functional interplay of histone lysine butyrylation, crotonylation, and acetylation in rice under starvation and submergence.
Genome biology . 2018-09-25 [PMID: 30253806]
Basic Information:
Sample Characteristic:
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Experimental Variables:
Assessing Quality:
Data Resource GEN Sample ID GEN Dataset ID Project ID BioProject ID Sample ID Sample Name BioSample ID Sample Accession Experiment Accession Release Date Submission Date Update Date Species Race Ethnicity Age Age Unit Gender Source Name Tissue Cell Type Cell Subtype Cell Line Disease Disease State Development Stage Mutation Phenotype Case Detail Control Detail Growth Protocol Treatment Protocol Extract Protocol Library Construction Protocol Molecule Type Library Layout Strand-Specific Library Strand Spike-In Strategy Platform Instrument Model Cell Number Reads Number Gbases AvgSpotLen1 AvgSpotLen2 Uniq Mapping Rate Multiple Mapping Rate Coverage Rate