2017
DOI: 10.1038/s41598-017-09299-7
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RNA-Seq analysis on chicken taste sensory organs: An ideal system to study organogenesis

Abstract: RNA-Seq is a powerful tool in transcriptomic profiling of cells and tissues. We recently identified many more taste buds than previously appreciated in chickens using molecular markers to stain oral epithelial sheets of the palate, base of oral cavity, and posterior tongue. In this study, RNA-Seq was performed to understand the transcriptomic architecture of chicken gustatory tissues. Interestingly, taste sensation related genes and many more differentially expressed genes (DEGs) were found between the epithel… Show more

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Cited by 12 publications
(11 citation statements)
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References 79 publications
(75 reference statements)
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“…High-throughput sequencing techniques have become powerful and effective tools for gaining a deeper understanding of the basic molecular mechanisms of complicated systems ( Wang et al, 2009 ; Ozsolak and Milos, 2011 ). RNA sequencing, a high-throughput technique, has been generally used in livestock to find the expression patterns of functional genes ( Cui et al, 2017 ; Ni et al, 2019 ; Peng et al, 2019 ).…”
Section: Introductionmentioning
confidence: 99%
“…High-throughput sequencing techniques have become powerful and effective tools for gaining a deeper understanding of the basic molecular mechanisms of complicated systems ( Wang et al, 2009 ; Ozsolak and Milos, 2011 ). RNA sequencing, a high-throughput technique, has been generally used in livestock to find the expression patterns of functional genes ( Cui et al, 2017 ; Ni et al, 2019 ; Peng et al, 2019 ).…”
Section: Introductionmentioning
confidence: 99%
“…A clusterProfiler R package was used to perform Gene Ontology (GO) enrichment analysis and to test the statistical enrichment of differential expression genes in the Kyoto encyclopedia of genes and genomes (KEGG) pathways. GO terms and KEGG terms with P value less than 0.05 were considered significantly enriched by DEGs [39, 40].…”
Section: Methodsmentioning
confidence: 99%
“…Tongues were collected and bathed in (E11.5) or sub-epithelially injected (P1) with collagenase A (1 mg/mL Sigma Aldrich, 10103586001) and dispase II (2.5 mg/mL Sigma Aldrich, 04942078001) for 30 min at 37 °C, then tongue epithelium was separated from mesenchyme. RNA was extracted as previously described [15] and after normalization converted to cDNA using Thermo Fisher's SuperScript™ First-Strand Synthesis System for RT-PCR.…”
Section: Rna Extraction Rt-qpcr and Rna-sequencingmentioning
confidence: 99%
“…RNA-sequencing was carried out and analyzed as previously described [15]. Fragments Per Kilobase of transcript per Million mapped reads (FPKM) values were utilized to represent gene expression levels.…”
Section: Rna Extraction Rt-qpcr and Rna-sequencingmentioning
confidence: 99%