bioRxivGenomicsPreprint
A direct link between Prss53, hair curvature, and skeletal dysplasia
Jichao DengiD, Yuning SongiD, Hongmei LiuiD, Tingting SuiiD, Mao CheniD, Yuxin ZhangiD, Bing YaoiD, Yuxin Xu, Zhiquan LiuiD, Liangxue LaiiD, Zhanjun LiiD
Abstract
In humans, protease serine S1 family member 53 (Prss53) is highly expressed in the hair follicle, especially the inner root sheath, which is associated with hair shape according to recent genome-wide association study (GWAS) data. However, no animal evidence has indicated a link between Prss53 and hair shape to date. Here, we used CRISPR/Cas9 to generate Prss53-mutated rabbits. The homozygous (Prss53-/-) rabbits exhibited curved hair and skeletal dyskinesia with severe malformation, while the heterozygous (Prss53+/-) rabbits did not exhibit these features. The curvature features of the hair were accompanied by lesions that were generally denser and less well-defined in the cuticular septation of the hair shaft, and the compartments of the hair follicle were incomplete, as evidenced by decreased expression levels of keratinocyte differentiation genes. In addition, skeletal dysplasia, an increased lethality rate and decreased plasma calcium and serum alkaline phosphatase (ALP) levels were determined in the Prss53-/- rabbits. Furthermore, disrupted calcium metabolism, which may play a role in the hair curvature and skeletal dysplasia of Prss53+/- rabbits, was demonstrated by using high-throughput RNA sequencing data. Thus, our study confirmed for the first time that the loss of Prss53 lead to curved hair in animals and provides new insights into the crucial role of Prss53 in calcium metabolism. Author SummaryNo animal evidence has indicated a link between Prss53 and hair shape to date. The Prss53-/- rabbits exhibited curved hair and skeletal dyskinesia. The disrupted calcium metabolism may play a role in the hair curvature and skeletal dysplasia of Prss53+/- rabbits.
- Citations
- 2
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A frameshift mutation in PRICKLE1 causes skeletal dysplasia in Cheviot sheep
Oswald Matika, Megan G. Davey, … Alan L. Archibald·bioRxiv·Oct 9, 2026
- Rab35 is required for embryonic development and kidney and ureter homeostasis through regulation of epithelial cell junctions
K. R. Clearman, N. Timpratoom, … B. K. Yoder·Journal of the American Society of NephrologyPeer-reviewed·Mar 26, 2024
- Gestational inhibition of CSF1R signaling using PLX5622 drives musculoskeletal changes in postnatal offspring
Rouzbeh Ostadsharif Memar, Matthew Rosin, … Jessica M. Rosin·Cells and DevelopmentPeer-reviewed·Aug 14, 2026
- Ap2s1 mutation in mice causes familial hypocalciuric hypercalcemia type 3
Fadil M. Hannan, Mark Stevenson, … Rajesh V. Thakker·bioRxiv·Aug 10, 2020
- Divergent genetic mechanisms lead to spiny hair in mammals
GISLENE LOPES GONÇALVES, Renan Maestri, … Hopi E. Hoekstra·PLoS ONEPeer-reviewed·Aug 17, 2018
- PDGFRα signaling regulates Srsf3 transcript binding to affect PI3K signaling and endosomal trafficking
Thomas E. Forman, Marcin Piotr Sajek, … Katherine A. Fantauzzo·eLifePeer-reviewed·Dec 4, 2024