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SRX8166390: GSM4494376: ACTTRAPH; Solanum lycopersicum; OTHER
2 ILLUMINA (Illumina HiSeq 4000) runs: 9.8M spots, 500.7M bases, 191.1Mb downloads

Submitted by: NCBI (GEO)
Study: Atlas of chromatin accessibility and translatome of tomato and rice root tip cell types
show Abstracthide Abstract
Plant species have evolved specialized cell types and regulatory programs. To understand this diversity, we profiled tomato cell type translatomes and chromatin accessibility. While cell type expression signatures are diverse, some genes exhibit robust cell type expression across time and environments. Using xylem differentiation as a model, newly described, repurposed and conserved genes illustrate this spatial variation. Data integration into regulatory networks demonstrates the function of molecularly uncharacterized cell types. Analyses of rice, tomato and Arabidopsis tissues suggest that root meristems are more conserved, while other cell types/tissues exhibit species-specific genes and processes. Several transcriptional properties observed in animals were also observed in plants and suggest cross-kingdom higher-order organizational properties. These data serve as a community resource, paving the way for engineering resilient crops. Overall design: Examination of cell type-specific ATAC and TRAP seq profiles in tomato and rice roots. Tomato plate-based experiments (the nuclear and translating ribosome affinity purification experiments) were conducted with four independent replicates of each of the 12 lines, with T1 seed stocks (and T2 as needed). Tomato pot-based experiments were conducted with four independent replicates of the meristematic cortex and cortex lines and each root tissue was dissected for the lateral roots and the adventitious (hypocotyl-derived) roots. Following filtering steps only four samples were included, one lateral and one adventitious root sample of the meristematic cortex and cortex lines. Tomato field-based experiment was performed with six independent replicates of the meristematic cortex, endodermis, meristematic zone and 35S lines. Following filtering steps, one replicate was removed from the endodermis and one from the meristematic cortex. Rice plate-based experiments were conducted with three independent replicates of the endodermis, vasculature and 35S lines, with T1 seed stocks (and T2 as needed), except for the meristematic cortex for which two independent replicates of two lines were used. Arabidopsis plate-based experiments were done with two independent replicates of the meristematic cortex, endodermis, vasculature and 35S lines as described in Mustroph et al., 2009.
Sample: ACTTRAPH
SAMN14680020 • SRS6527668 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 4000
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: SINGLE
Construction protocol: Translating Ribosome Affinity Purification (TRAP) was performed as previously described (Reynoso et al. 2019). RNA-seq libraries were prepared from poly(A)+ selected total and TRAP mRNA as described by Townsley et al. (2014) for random primer primed libraries.
Experiment attributes:
GEO Accession: GSM4494376
Links:
Runs: 2 runs, 9.8M spots, 500.7M bases, 191.1Mb
Run# of Spots# of BasesSizePublished
SRR115995514,882,607249M95.1Mb2021-03-24
SRR115995524,935,278251.7M96Mb2021-03-24

ID:
10643623

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