Profiling the landscape of transcription, chromatin accessibility and chromosome conformation of cattle, pig, chicken and goat genomes [FAANG pilot project]

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Foissac, Sylvain | Djebali Quelen, Sarah | Acloque, Hervé | Bardou, Philippe | Blanc, Fany | Cabau, Cédric | Derrien, Thomas | Drouet, Françoise | Esquerre, Diane | Fabre, Stéphane | Gaspin, Christine | González, Ignacio | Goubil, Adeline | Klopp, Christophe | Laurent, Fabrice | Marthey, Sylvain | Marti-Marimon, Maria | Mompart, Florence | Munyard, Kylie | Muret, Kévin | Pollet, Sophie | Quéré, Pascale | Rau, Andrea | Robelin, David | San Cristobal, Magali | Tixier-Boichard, Michèle | Tosser-Klopp, Gwenola | Villa-Vialaneix, Nathalie | Vincent-Naulleau, Silvia | Zytnicki, Matthias | Pinard-van Der Laan, Marie-Hélène | Lagarrigue, Sandrine | Giuffra, Elisabetta

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Functional annotation of livestock genomes is a critical and obvious next step to derive maximum benefit for agriculture, animal science, animal welfare and human health. The aim of the Fr-AgENCODE project is to generate multi-species functional genome annotations by applying high-throughput molecular assays on three target tissues/cells relevant to the study of immune and metabolic traits. An extensive collection of stored samples from other tissues is available for further use (FAANG Biosamples ‘FR-AGENCODE’). From each of two males and two females per species (pig, cattle, goat, chicken), strand-oriented RNA-seq and chromatin accessibility ATAC-seq assays were performed on liver tissue and on two T-cell types (CD3+CD4+&CD3+CD8+) sorted from blood (mammals) or spleen (chicken). Chromosome Conformation Capture (in situ Hi-C) was also carried out on liver. Sequencing reads from the 3 assays were processed using standard processing pipelines. While most (50–70%) RNA-seq reads mapped to annotated exons, thousands of novel transcripts and genes were found, including extensions of annotated protein-coding genes and new lncRNAs (see abstract #69857). Consistency of ATAC-seq results was confirmed by the significant proportion of called peaks in promoter regions (36–66%) and by the specific accumulation pattern of peaks around gene starts (TSS) v. gene ends (TTS). Principal Component Analyses for RNA-seq (based on quantified gene expression) and ATAC-seq (based on quantified chromatin accessibility) highlighted clusters characterised by cell type and sex in all species. From Hi-C data, we generated 40kb-resolution interaction maps, profiled a genome-wide Directionality Index and identified from 4,100 (chicken) to 12,100 (pig) topologically-associating do- mains (TADs). Correlations were reported between RNA-seq and ATAC-seq results (see abstract #71581). In summary, we present here an overview of the first multi-species and -tissue annotations of chromatin accessibility and genome architecture related to gene expression for farm animals.

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