Mutation of the Thap4 gene causes dwarfism and testicular anomalies in rats and mice.
Kentaro KatayamaJunya ItoRei MurakamiAyako YamashitaHotaka SasajimaSatomi NarahashiJunko ChibaIchiro YamamotoWataru FujiiYuki TochigiHiroetsu SuzukiPublished in: Mammalian genome : official journal of the International Mammalian Genome Society (2024)
The petit (pet) locus is associated with dwarfism, testicular anomalies, severe thymic hypoplasia, and high postnatal lethality, which are inherited in autosomal recessive mode of inheritance in rats with a Wistar strain genetic background. Linkage analysis localized the pet locus between 98.7 Mb and 101.2 Mb on rat chromosome 9. Nucleotide sequence analysis identified 2 bp deletion in exon 2 of the Thap4 gene as the causative mutation for pet. This deletion causes a frameshift and premature termination codon, resulting in a truncated THAP4 protein lacking approximately two-thirds of the C-terminal side. Thap4 is expressed in various organs, including the testis and thymus in rats. To elucidate the biological function of THAP4 in other species, we generated Thap4 knockout mice lacking exon 2 of the Thap4 gene through genome editing. Thap4 knockout mice also exhibited dwarfism and small testis but did not show high postnatal lethality. Thymus weights of adult Thap4 knockout male mice were significantly higher compared to wild-type male mice. Although Thap4 knockout male mice were fertile, their testis contained seminiferous tubules with spermatogenesis and degenerative seminiferous tubules lacking germ cells. Additionally, we observed vacuoles in seminiferous tubules, and clusters of cells in the lumen in seminiferous tubules in Thap4 knockout male mice. These results demonstrate that spontaneous mutation of Thap4 gene in rats and knockout of Thap4 gene in mice both cause dwarfism and testicular anomalies. Thap4 gene in rats and mice is essential for normal testicular development, maintaining spermatogenesis throughout the entire region of seminiferous tubules.
Keyphrases
- copy number
- wild type
- genome wide
- germ cell
- genome editing
- mitochondrial dna
- computed tomography
- genome wide identification
- pet ct
- crispr cas
- induced apoptosis
- positron emission tomography
- dna methylation
- preterm infants
- metabolic syndrome
- cell death
- skeletal muscle
- human immunodeficiency virus
- high fat diet induced
- amino acid
- insulin resistance
- intellectual disability
- early onset
- hiv infected
- drug induced
- antiretroviral therapy
- genetic diversity
- binding protein