The gyrfalcon (Falco rusticolus) genome

Author:

Zuccolo Andrea12ORCID,Mfarrej Sara3ORCID,Celii Mirko1ORCID,Mussurova Saule1,Rivera Luis F1ORCID,Llaca Victor4ORCID,Mohammed Nahed1ORCID,Pain Arnab3ORCID,Alrefaei Abdulmajeed Fahad5ORCID,Alrefaei Abdulwahed Fahad6ORCID,Wing Rod A17ORCID

Affiliation:

1. Center for Desert Agriculture (CDA), Biological and Environmental Sciences & Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST) , Thuwal 23955-6900 , Saudi Arabia

2. Crop Science Research Center, Sant’Anna School of Advanced Studies , Piazza Martiri della Libertà 33, 56127 Pisa , Italy

3. King Abdullah University of Science and Technology (KAUST), Pathogen Genomics Laboratory, Biological and Environmental Science and Engineering (BESE) , Thuwal-Jeddah 23955-6900 , Saudi Arabia

4. Research and Development, Corteva Agriscience , Johnston, IA 50131 , USA

5. Department of Biology, Jamoum University College, Umm Al-Qura University , Mecca 24382 , Saudi Arabia

6. Department of Zoology, College of Science, King Saud University , P.O. Box 2455, Riyadh 11451 , Saudi Arabia

7. School of Plant Sciences, Arizona Genomics Institute, University of Arizona , 24 Tucson, Arizona 85721 , USA

Abstract

Abstract High-quality genome assemblies are characterized by high-sequence contiguity, completeness, and a low error rate, thus providing the basis for a wide array of studies focusing on natural species ecology, conservation, evolution, and population genomics. To provide this valuable resource for conservation projects and comparative genomics studies on gyrfalcon (Falco rusticolus), we sequenced and assembled the genome of this species using third-generation sequencing strategies and optical maps. Here, we describe a highly contiguous and complete genome assembly comprising 20 scaffolds and 13 contigs with a total size of 1.193 Gbp, including 8,064 complete Benchmarking Universal Single-Copy Orthologs (BUSCOs) of the total 8,338 BUSCO groups present in the library aves_odb10. Of these BUSCO genes, 96.7% were complete, 96.1% were present as a single copy, and 0.6% were duplicated. Furthermore, 0.8% of BUSCO genes were fragmented and 2.5% (210) were missing. A de novo search for transposable elements (TEs) identified 5,716 TEs that masked 7.61% of the F. rusticolus genome assembly when combined with publicly available TE collections. Long interspersed nuclear elements, in particular, the element Chicken-repeat 1 (CR1), were the most abundant TEs in the F. rusticolus genome. A de novo first-pass gene annotation was performed using 293,349 PacBio Iso-Seq transcripts and 496,195 transcripts derived from the assembly of 42,429,525 Illumina PE RNA-seq reads. In all, 19,602 putative genes, of which 59.31% were functionally characterized and associated with Gene Ontology terms, were annotated. A comparison of the gyrfalcon genome assembly with the publicly available assemblies of the domestic chicken (Gallus gallus), zebra finch (Taeniopygia guttata), and hummingbird (Calypte anna) revealed several genome rearrangements. In particular, nine putative chromosome fusions were identified in the gyrfalcon genome assembly compared with those in the G. gallus genome assembly. This genome assembly, its annotation for TEs and genes, and the comparative analyses presented, complement and strength the base of high-quality genome assemblies and associated resources available for comparative studies focusing on the evolution, ecology, and conservation of Aves.

Funder

KAUST

R.A.W

Green Sustainability Company

Environmental Services

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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