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SRX11715656: GSM5513384: SW_sr_TT_krh_rep_3; Quercus robur; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 41.2M spots, 12.5G bases, 3.6Gb downloads

Submitted by: NCBI (GEO)
Study: RNA-seq analysis of different parts of Quercus robur seedling root
show Abstracthide Abstract
As an adaptive response to the environment, oaks have evolved long taproots that increase their ability to acquire water. Taproots penetrate deeper layers of soil and send out absorptive roots that can then uptake water from these layers. This ability enables taproots to supply trees with water better. Unfortunately, the applied agrotechnical procedures during seedlings production in container nurseries damage the oaks' taproot, leading to changes in the root system structure. That changes may make the seedlings more responsive to chronic or periodic episodes of severe drought. In turn, seedlings that containers do not restrict roots growth, i.e. grown in rhizotron, may elongate because they are not subjected to air-pruning. Despite their significant role, little is known about the internal factors (specific genes) and their interactions that regulate taproot elongation in oaks seedlings. Thus, our study aimed to determine the potential genes regulating growth, cessation and physiology of taproot and check whether there is a difference in the expression level of the genes involved in root development. For this purpose, we performed next-generation sequencing (NGS), taproots and lateral roots, which allowed us to obtain a complete picture of the transcriptomes. Our findings of taproot growth regulations can be used to improve trees production in forest nurseries. Overall design: Identification of genes involved in the regulation of taproot growth in containerized oak seedlings and seedlings sown directly in the soil.
Sample: SW_sr_TT_krh_rep_3
SAMN20704869 • SRS9746080 • All experiments • All runs
Organism: Quercus robur
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was isolated from the taproot containing the meristematic zone and the elongation zone, and from the lateral roots using a commercial GeneAll kit. RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM5513384
Links:
Runs: 1 run, 41.2M spots, 12.5G bases, 3.6Gb
Run# of Spots# of BasesSizePublished
SRR1541362541,249,76812.5G3.6Gb2022-11-23

ID:
15631777

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