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IGF2BP3 recognizes m<sup>6</sup>A to regulate histone-to-protamine replacement during mouse sperm development.


ABSTRACT: Post-meiotic development of spermatids is under the control of a sophisticated RNA metabolic network, wherein the N6-methyladenosine (m6A) modification of mRNA, and proteins that bind to it, exert crucial functions in regulating sperm development from spermatogonia to spermatocytes. However, which m6A recognition proteins are involved in male post-meiotic spermiogenesis, and via which regulatory mechanisms, remains largely unknown. Here, we uncover the involvement of the m6A reader protein IGF2BP3 in the regulation of post-meiotic spermatid development. Genetic ablation of Igf2bp3 results in spermatogenesis defects, leading to male sub-fertility or even infertility. Mechanistically, IGF2BP3 loss-of-function leads to the excessive translation of its target R

SUBMITTER: Wang D 

PROVIDER: S-EPMC12811620 | biostudies-literature | 2026 Jan

REPOSITORIES: biostudies-literature