Gene Expression Nebulas
A data portal of transcriptomic profiles analyzed by a unified pipeline across multiple species

Gene Expression Nebulas

A data portal of transcriptome profiles across multiple species

PRJNA684474: Transcriptome analysis reveals photoperiod-associated genes expressed in rice anthers

Source: NCBI / GSE163030
Submission Date: Dec 11, 2020
Release Date: Jan 13, 2021
Update Date: Apr 14, 2021

Summary: Environmental conditions, such as photoperiod and temperature, can affect male fertility in plants. While this feature is heavily exploited in rice to generate male-sterile lines for hybrid breeding, the underlying molecular mechanisms remain largely unknown. In this study, we use a transcriptomics approach to identify key genes and regulatory networks affecting pollen maturation in rice anthers in response to different day lengths.This work provides a new understanding on photoperiodsensitive pollen development in rice, and our gene expression database will provide a new, comprehensive resource to identify new environmentally sensitive genes regulating male fertility for use in crop improvement.

Overall Design: the mitosis stages I anther were collected at 08:00,12:00,16:00,20:00,00:00, 04:00 in sort-day(12 hours light) and long-day(14 hours dark) condition., each sample have two biological replicates.

GEN Datasets:
GEND000527
Strategy:
Species:
Tissue:
Healthy Condition:
Cell Type:
Cell Line:
Development Stage:
Protocol
Growth Protocol: Rice variety Oryza sativa L. ssp. japonica 9522 was grown in paddy fields around Shanghai (China) during the normal rice growing season (June–August).
Treatment Protocol: Photoperiod treatment was started after panicle initiation and continued until all samples were collected: LD was the natural daylight condition, with a photoperiod of ~14 h; SD conditions were simulated by covering plants with black cloth for the last 2 h of natural daylight to create a 12 h photoperiod.
Extract Protocol: RNA was harvested using Trizol reagent (Invitrogen).
Library Construction Protocol: RNA library using standard Ion proton RNA-Seq Kit v2.0 protocol
Sequencing
Molecule Type: rRNA- RNA
Library Source:
Library Layout: SINGLE
Library Strand: Reverse
Platform: ION_TORRENT
Instrument Model: Ion Torrent Proton
Strand-Specific: Specific
Samples
Basic Information:
Sample Characteristic:
Biological Condition:
Experimental Variables:
Protocol:
Sequencing:
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 Condition 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