
We aimed to demonstrate feasibility of functional validation of osteoporosis candidate genes through crispant screening, we compared a crispant to a stable KO zebrafish model for the lrp5 gene. In humans, recessive loss of function mutations in LRP5, a co receptor in the Wnt signaling pathway, cause osteoporosis pseudoglioma syndrome. In conclusion, we show through faithful modeling of LRP5 related primary osteoporosis that crispant screening in zebrafish is a promising approach for rapid functional screening of osteoporosis candidate genes.
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