YIPF5 (p.W218R) mutation induced primary microcephaly in rabbits

Autor: Xin Liu, Jie Yang, Zhaoyi Li, Ruonan Liu, Xinyu Wu, Zhongtian Zhang, Liangxue Lai, Zhanjun Li, Yuning Song
Jazyk: angličtina
Rok vydání: 2023
Předmět:
Zdroj: Neurobiology of Disease, Vol 182, Iss , Pp 106135- (2023)
Druh dokumentu: article
ISSN: 1095-953X
20343418
DOI: 10.1016/j.nbd.2023.106135
Popis: Primary microcephaly (PMCPH) is a rare autosomal recessive neurodevelopmental disorder with a global prevalence of PMCPH ranging from 0.0013% to 0.15%. Recently, a homozygous missense mutation in YIPF5 (p.W218R) was identified as a causative mutation of severe microcephaly. In this study, we constructed a rabbit PMCPH model harboring YIPF5 (p.W218R) mutation using SpRY-ABEmax mediated base substitution, which precisely recapitulated the typical symptoms of human PMCPH. Compared with wild-type controls, the mutant rabbits exhibited stunted growth, reduced head circumference, altered motor ability, and decreased survival rates. Further investigation based on model rabbit elucidated that altered YIPF5 function in cortical neurons could lead to endoplasmic reticulum stress and neurodevelopmental disorders, interference of the generation of apical progenitors (APs), the first generation of progenitors in the developing cortex. Furthermore, these YIPF5-mutant rabbits support a correlation between unfolded protein responses (UPR) induced by endoplasmic reticulum stress (ERS), and the development of PMCPH, thus providing a new perspective on the role of YIPF5 in human brain development and a theoretical basis for the differential diagnosis and clinical treatment of PMCPH. To our knowledge, this is the first gene-edited rabbit model of PMCPH. The model better mimics the clinical features of human microcephaly than the traditional mouse models. Hence, it provides great potential for understanding the pathogenesis and developing novel diagnostic and therapeutic approaches for PMCPH.
Databáze: Directory of Open Access Journals
Externí odkaz: