U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from BioSample

SRX711187: GSM1514701: TIL15_GCTAT.PL17; Zea mays; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 12.3M spots, 1.2G bases, 822.3Mb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Zea mays Transcriptome or Gene expression
show Abstracthide Abstract
Modification of cis regulatory elements to produce differences in gene expression level, localization, and timing is an important mechanism by which organisms evolve divergent adaptations. To examine gene regulatory change during the domestication of maize from its wild progenitor, teosinte, we assessed allele-specific expression in a collection of maize and teosinte inbreds and their F1 hybrids using three tissues from different developmental stages. Our use of F1 hybrids represents the first study in a domesticated crop and wild progenitor that dissects cis and trans regulatory effects to examine characteristics of genes under various cis and trans regulatory regimes. We find evidence for consistent cis regulatory divergence that differentiates maize from teosinte in approximately 4% of genes. These genes are significantly correlated with genes under selection during domestication and crop improvement, suggesting an important role for cis regulatory elements in maize evolution. Overall design: We assayed genome-wide cis and trans regulatory differences between maize and its wild progenitor, teosinte, using deep RNA sequencing in F1 hybrid and parent inbred lines for three tissue types (ear, leaf and stem) followed by assessment of allele-specific gene expression.
Sample: TIL15_GCTAT.PL17
SAMN03081959 • SRS709933 • All experiments • All runs
Organism: Zea mays
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was extracted from the plant tissues using a standard TRIzol protocol, quantified by spectrophotometer, and normalized to 1 ììin nuclease free water. We generated polyA selected, strand specific, barcoded RNAseq libraries using a five minute fragmentation time and 12 PCR amplification cycles. Library adapters used balanced barcode sequences of four and five base pairs. Pools of 14 (F1s) or 15 (parents) libraries were sequenced on one Illumina lane each
Experiment attributes:
GEO Accession: GSM1514701
Links:
External link:
Runs: 1 run, 12.3M spots, 1.2G bases, 822.3Mb
Run# of Spots# of BasesSizePublished
SRR158691112,319,5401.2G822.3Mb2014-11-06

ID:
1002381

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...