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SRX5255215: GSM3564912: LT_FB_L_R2; Lentinus tigrinus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 15.1M spots, 3.8G bases, 1.2Gb downloads

Submitted by: NCBI (GEO)
Study: Transcriptomic atlas of mushroom development reveals conserved genes behind complex multicellularity in fungi [Lentinus tigrinus]
show Abstracthide Abstract
The evolution of complex multicellularity has been one of the major transitions in the history of life. In contrast to simple multicellular aggregates of cells, it has evolved only in a handful of lineages, including the animals, embryophytes, red and brown algae and fungi. Despite being a key step towards the evolution of complex organisms, the evolutionary origins and the genetic underpinnings of complex multicellularity are incompletely known. We constructed a reference atlas of mushroom formation based on developmental transcriptome data of six species and comparisons of >200 whole genomes, to elucidate the core genetic program of complex multicellularity and fruiting body development in mushroom-forming fungi (Agaricomycetes). Nearly 300 conserved gene families and >70 functional groups contained developmentally regulated genes from five to six species, covering functions related to fungal cell wall (FCW) remodeling, targeted protein degradation, signal transduction, adhesion and small secreted proteins (including effector-like orphan genes). Several of these families, including F-box proteins, expansin-like proteins, protein kinases, and transcription factors, showed expansions in Agaricomycetes, with from which many convergently expandedwere identified in multicellular plants and/or animals too, assuming convergent solutions to genetic hurdles imposed by complex multicellularity among independently evolved lineages. This study provides a novel entry point to studying mushroom development and complex multicellularity in one of the largest clades of complex eukaryotic organisms. Overall design: 27 samples corresponding to 9 developmental stages were analyzed. Developmental stages contain 3 biological replicates.
Sample: LT_FB_L_R2
SAMN10756331 • SRS4256728 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: After harvesting, samples were immediately placed on liquid nitrogen and stored at -80 °C until use. 50-75 mg frozen tissue was placed in a pre-chilled mortar and ground to a fine powder. RNeasy Midi Kit (QIAGEN) was used for RNA extraction according to manufacturer«s instructions. Whole transcriptome sequencing was performed using the TrueSeq RNA Library Preparation Kit v2 (Illumina) according to the manufacturer's instructions. Briefly, RNA quality and quantity measurements were performed using RNA ScreenTape and Reagents on TapeStation (all from Agilent) and Qubit (ThermoFisher); only high quality (RIN >8.0) total RNA samples were processed. Next, RNA was DNaseI (ThermoFisher) treated and the mRNA was purified and fragmented. First strand cDNA synthesis was performed using SuperScript II (ThermoFisher) followed by second strand cDNA synthesis, end repair, 3'-end adenylation, adapter ligation and PCR amplification. All of the purification steps were performed using AmPureXP Beads (Backman Coulter). Final libraries were quality checked using D1000 ScreenTape and Reagents on TapeStation (all from Agilent). Concentration of each library was determined using either the QPCR Quantification Kit for Illumina (Agilent) or the KAPA Library Quantification Kit for Illumina (KAPA Biosystems)
Experiment attributes:
GEO Accession: GSM3564912
Links:
Runs: 1 run, 15.1M spots, 3.8G bases, 1.2Gb
Run# of Spots# of BasesSizePublished
SRR844820215,075,1843.8G1.2Gb2019-03-17

ID:
7091281

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