scholarly journals Editorial: Functional Annotation of Animal Genomes

2021 ◽  
Vol 12 ◽  
Author(s):  
Amanda Jane Chamberlain ◽  
Hans H. Cheng ◽  
Elisabetta Giuffra ◽  
Christa Kuehn ◽  
Christopher K. Tuggle ◽  
...  
2016 ◽  
Vol 47 (5) ◽  
pp. 528-533 ◽  
Author(s):  
Christopher K. Tuggle ◽  
Elisabetta Giuffra ◽  
Stephen N. White ◽  
Laura Clarke ◽  
Huaijun Zhou ◽  
...  

Author(s):  
Emily L Clark ◽  
Alan L Archibald ◽  
Hans D Daetwyler ◽  
Martien AM Groenen ◽  
Peter W Harrison ◽  
...  

Here we review and describe a set of research priorities to meet present and future challenges posed to farmed animal production that build on progress, successes and resources from the Functional Annotation of ANimal Genomes (FAANG) project.


2019 ◽  
Vol 97 (Supplement_2) ◽  
pp. 17-17
Author(s):  
Christopher K Tuggle ◽  
Elisabetta Giuffra

Abstract The annotation of the functional components of genomes is required for both basic and applied genomic research, yet farmed animal genomics are deficient in such annotation. This talk will introduce the Functional Annotation of ANimal Genomes (FAANG) consortium, which was initiated in 2014 to address this knowledge deficit. An overarching theme of early FAANG efforts is the collaborative approach required for such comprehensive research, thus another emphasis of this talk will be our community efforts to develop the environment for successful FAANG research. FAANG scientists have created a coordinated data collection and analysis enterprise crucial for success of this global effort, and funding of ~$20 million has been secured for current projects in several species, with an anticipated doubling of this support during 2019. Member FAANG consortium labs are producing genome-wide datasets on RNA expression, DNA methylation, chromatin modification, chromatin accessibility, and chromatin interactions for many agriculturally relevant animal species. The goal of a first-generation global chromatin state map for cattle, chicken, pig, and potentially other species is projected for completion in the next 3–5 years. These data will be used both to better understand animal genome function at the epigenetic level, as well as improve the precision and sensitivity of genomic selection for animal improvement. The functional annotation delivered by the FAANG initiative will add value and utility to the greatly improved genome sequences being established for domesticated animal species.


2021 ◽  
Vol 12 ◽  
Author(s):  
Sichong Peng ◽  
Rebecca Bellone ◽  
Jessica L. Petersen ◽  
Theodore S. Kalbfleisch ◽  
Carrie J. Finno

An assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) has become an increasingly popular method to assess genome-wide chromatin accessibility in isolated nuclei from fresh tissues. However, many biobanks contain only snap-frozen tissue samples. While ATAC-seq has been applied to frozen brain tissues in human, its applicability in a wide variety of tissues in horse remains unclear. The Functional Annotation of Animal Genome (FAANG) project is an international collaboration aimed to provide high quality functional annotation of animal genomes. The equine FAANG initiative has generated a biobank of over 80 tissues from two reference female animals and experiments to begin to characterize tissue specificity of genome function for prioritized tissues have been performed. Due to the logistics of tissue collection and storage, extracting nuclei from a large number of tissues for ATAC-seq at the time of collection is not always practical. To assess the feasibility of using stored frozen tissues for ATAC-seq and to provide a guideline for the equine FAANG project, we compared ATAC-seq results from nuclei isolated from frozen tissue to cryopreserved nuclei (CN) isolated at the time of tissue harvest in liver, a highly cellular homogenous tissue, and lamina, a relatively acellular tissue unique to the horse. We identified 20,000–33,000 accessible chromatin regions in lamina and 22–61,000 in liver, with consistently more peaks identified using CN isolated at time of tissue collection. Our results suggest that frozen tissues are an acceptable substitute when CN are not available. For more challenging tissues such as lamina, nuclei extraction at the time of tissue collection is still preferred for optimal results. Therefore, tissue type and accessibility to intact nuclei should be considered when designing ATAC-seq experiments.


2018 ◽  
Vol 49 (6) ◽  
pp. 564-570 ◽  
Author(s):  
E. N. Burns ◽  
M. H. Bordbari ◽  
M. J. Mienaltowski ◽  
V. K. Affolter ◽  
M. V. Barro ◽  
...  

2015 ◽  
Vol 16 (1) ◽  
Author(s):  
Leif Andersson ◽  
◽  
Alan L Archibald ◽  
Cynthia D Bottema ◽  
Rudiger Brauning ◽  
...  

2019 ◽  
Vol 97 (Supplement_2) ◽  
pp. 15-16
Author(s):  
Sylvain Foissac ◽  
Sarah Djebali ◽  
Kylie Munyard ◽  
Nathalie Vialaneix ◽  
Andrea Rau ◽  
...  

Abstract Improving the functional annotation of animal genomes is a key challenge in bridging the gap between genotype and phenotype, thus enabling predictive biology. Regarding livestock production, major outcomes are expected from a better understanding of the genetic architecture underlying quantitative traits. As part of the Functional Annotation of ANimal Genomes action (FAANG: www.faang.org), the FR-AgENCODE project generated omics data to improve the reference annotation of the cattle, pig, goat and chicken genome. High-throughput molecular assays have been performed on tissues/cells relevant to immune and metabolic traits. From two males and two females per species (pig, cattle, goat, chicken), strand-oriented RNA-seq gene expression and ATAC-seq chromatin accessibility assays were performed on liver and two PBMC-sorted T-cell types (CD4+ and CD8+). Chromosome Conformation Capture (in situ Hi-C) was also carried out on liver samples. About 4,000 samples have been collected at the INRA biorepository and registered at the EBI BioSamples registry. More than 80% of the planned experiments could be completed, generating ~11.5 billions of sequencing reads over the 3 assays. While most (50–80%) RNA-seq reads mapped to annotated exons, thousands of novel transcripts were found, with ~60K mRNAs and ~22K lncRNAs in cattle. Differentially expressed genes between cell types were enriched for immunity- or metabolism-related terms, and differentially accessible chromatin regions were identified as potential regulatory sites. Interestingly, correlations between gene expression and promoter accessibility across samples were skewed towards both positive and negative values, suggesting distinct regulatory mechanisms of gene expression. These patterns have been further investigated using human data from the Epigenome Roadmap Mapping Consortium. Altogether, this study illustrates the interest of a coordinated effort to tackle the genome-to-phenome challenge and provides a useful resource to the community. Availability: www.fragencode.org.


2019 ◽  
Vol 7 (1) ◽  
pp. 65-88 ◽  
Author(s):  
Elisabetta Giuffra ◽  
Christopher K. Tuggle ◽  

Functional annotation of genomes is a prerequisite for contemporary basic and applied genomic research, yet farmed animal genomics is deficient in such annotation. To address this, the FAANG (Functional Annotation of Animal Genomes) Consortium is producing genome-wide data sets on RNA expression, DNA methylation, and chromatin modification, as well as chromatin accessibility and interactions. In addition to informing our understanding of genome function, including comparative approaches to elucidate constrained sequence or epigenetic elements, these annotation maps will improve the precision and sensitivity of genomic selection for animal improvement. A scientific community–driven effort has already created a coordinated data collection and analysis enterprise crucial for the success of this global effort. Although it is early in this continuing process, functional data have already been produced and application to genetic improvement reported. The functional annotation delivered by the FAANG initiative will add value and utility to the greatly improved genome sequences being established for domesticated animal species.


2018 ◽  
Author(s):  
Su Datt Lam ◽  
Christine Orengo ◽  
Jonathan Lees

ABSTRACTAlternative splicing (AS) has been suggested as one of the major processes expanding the diversity of proteomes in multicellular organisms. Mutually exclusive exons (MXE) provide one form of AS that is less likely to disrupt protein structure and is over-represented in the proteome compared to other forms of AS. We used domain structure information from the CATH classification to perform a systematic structural analysis of the effects of MXE splicing in high quality animal genomes (e.g. human, fly, mouse and 2 fishes) and we were able to annotate approximately 50% of MXE events with structural information. For those MXE events which can be mapped to a structure, we found that although embedded in domains, they were strongly enriched in surface exposed residues. We also demonstrated that the variable residues between splicing events lie close to known and/or predicted functional sites. We present some examples of MXE events in proteins that have important roles in cells. This work presents the first large scale systematic study of the structural/functional effects of MXE splicing using predominantly domain based modelling and functional annotation tools. Our study supports and expands on previous work in this field and helps to build a picture of how MXE events facilitate evolution of new functions.


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