U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from BioSample

ERX3336768: NextSeq 500 paired end sequencing; Evidence of developmental escape from transcriptional-gene-silencing in MESSI retrotransposons
1 ILLUMINA (NextSeq 500) run: 43.4M spots, 6.5G bases, 2.5Gb downloads

Design: Evidence of developmental escape from transcriptional-gene-silencing in MESSI retrotransposons
Submitted by: IFEVA (CONICET-UBA)
Study: Evidence of developmental escape from transcriptional-gene-silencing in MESSI retrotransposons
show Abstracthide Abstract
The intent of the experiment was to infer, from transcriptome analysis, the occurrence of competent LTR retrotransposons in shoot apical meristems of Solanum lycopersicum. For this, we performed Illumina pair-end RNA-seq in M82 tomato samples of meristems, leaves and flowers. We also harvested meristems in plants subjected to long-term heat. In addition, we performed RNA-seq in meristems, leaves and flowers samples from Solanum pennellii, to aid phylogenetic interpretations.
Sample: Pennellii_Flowers_B
SAMEA5595499 • ERS3399709 • All experiments • All runs
Library:
Name: Pennellii_Flowers_B_p
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Construction protocol: Samples were harvested at the end of the day, and consisted of pools of at least a hundred whole shoot apical meristems, at least four open flowers, or at least six first leaves. Samples were collected from two or three week old plants of tomato or S. pennellii, respectively. Seeds were directly sown in soil (Levington F2, ICL) and stratified in the dark for one week at 4°C. Plants were grown in a Conviron MTPS chamber (Conviron) at 25/18°C (day/night); with 16/8 hours light cycle, 300 µmol/m2/s light intensity and ~60% humidity. For the heat treatment, plants were subjected to 35°C for 16 hours during a complete day period. Total RNA from shoot apical meristems was extracted with the PicoPure RNA Isolation kit (Life technologies), whereas the Plant-RNAeasy kit (Invitrogen) was used for flowers and leaves. Strand-specific libraries were prepared with 2 µg of RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina); following provider's instructions.
Experiment attributes:
Experimental Factor: organism: Solanum pennellii
Experimental Factor: organism part: leaf
Experimental Factor: stimulus: none
Runs: 1 run, 43.4M spots, 6.5G bases, 2.5Gb
Run# of Spots# of BasesSizePublished
ERR331125243,407,0536.5G2.5Gb2019-07-03

ID:
8475095

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...