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Introduction: Comprehensive genomic resources offer insights into biological features, including traits/disease-related genetic loci. The current reference genome assembly for the domestic cat (Felis catus), Felis_Catus_9.0 (felCat9), derived from sequences of the Abyssinian cat, may inadequately represent the general cat population, limiting the extent of deducible genetic variations.
Objectives: The goal was to develop Anicom American Shorthair 1.0 (AnAms1.0), a reference-grade chromosome-scale cat genome assembly.
Methods: In contrast to prior assemblies relying on Abyssinian cat sequences, AnAms1.0 was constructed from the sequences of more popular American Shorthair breed, which is related to more breeds than the Abyssinian cat. By combining advanced genomics technologies, including PacBio long-read sequencing and Hi-C- and optical mapping data-based sequence scaffolding, we compared AnAms1.0 to existing Felidae genome assemblies (20 scaffolds, scaffolds N50 > 150 Mbp). Homology-based and ab initio gene annotation through Iso-Seq and RNA-Seq was used to identify new coding genes and splice variants.
Results: AnAms1.0 demonstrated superior contiguity and accuracy than existing Felidae genome assemblies. Using AnAms1.0, we identified over 1.5 thousand structural variants and 29 million repetitions compared to felCat9. Additionally, we identified > 1,600 novel protein-coding genes. Notably, olfactory receptor structural variants and cardiomyopathy-related variants were identified.
Conclusion: AnAms1.0 facilitates the discovery of novel genes related to normal and disease phenotypes in domestic cats. The analyzed data are publicly accessible on Cats-I (https://cat.annotation.jp/), which we established as a platform for accumulating and sharing genomic resources to discover novel genetic traits and advance veterinary medicine.
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http://dx.doi.org/10.1016/j.jare.2024.10.023 | DOI Listing |
Can Vet J
April 2025
Department of Veterinary Internal Medicine and BK 21 project team, College of Veterinary Medicine, Chonnam National University, Gwangju 61186, Korea.
A 2-year-old male Abyssinian cat was presented with a left head tilt, lethargy, compulsive walking with a left-circling tendency, medial strabismus, a delayed pupillary light reflex, abdominal papules, and severe pruritus that began at 4 mo of age. Imaging revealed mineral opacity foci in the left ear, and magnetic resonance imaging confirmed heterogeneous signal changes, suggesting a diagnosis of otitis interna. No abnormal findings were observed on cerebrospinal fluid tests.
View Article and Find Full Text PDFVet Sci
December 2024
Department of Veterinary Science, Tokyo University of Agriculture and Technology, Tokyo 183-8509, Japan.
An eight-year-old spayed female Abyssinian cat presented with lameness. Palpation revealed swelling, heat, and a reduced range of motion in the stifle and tarsal joints in both hind limbs. A radiographic examination of both hind limbs revealed periosteal proliferation from the distal tibia to the tarsal and metatarsal bones, which suggested hypertrophic osteopathy.
View Article and Find Full Text PDFTierarztl Prax Ausg K Kleintiere Heimtiere
December 2024
Kleintierklinik, Ludwig-Maximilians-Universität München.
Two domestic cats (Abyssinian and Carthusian) presented with chronic respiratory signs including cough, respiratory sounds, and polypnea. One of the cats also showed intermittent fever. Thoracic radiographs demonstrated severe changes with predominantly micronodular interstitial lung patterns, some with mineralized areas.
View Article and Find Full Text PDFJ Adv Res
October 2024
National Institute of Genetics, Research Organization of Information and Systems, Mishima, Shizuoka, Japan. Electronic address:
J Vet Intern Med
May 2024
Laboratory of Veterinary Internal Medicine, Department of Veterinary Clinical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Background: X-linked dystrophin-deficient muscular dystrophy (MD) is a form of MD caused by variants in the DMD gene. It is a fatal disease characterized by progressive weakness and degeneration of skeletal muscles.
Hypothesis/objectives: Identify deleterious genetic variants in DMD by whole-genome sequencing (WGS) using a next-generation sequencer.