Lin28a/let-7Pathway Modulates theHoxCode viaPolycombRegulation during Axial Patterning in Vertebrates
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Abstract
The body plan along the anteroposterior axis and regional identities are specified by the spatiotemporal expression of Hox genes. Multistep controls are required for their unique expression patterns; however, the molecular mechanisms behind the tight control of Hox genes are not fully understood. In this study, we demonstrated that the Lin28a / let-7 reciprocal regulatory pathway is critical for vertebral specification. Lin28a −/− mice exhibited homeotic transformations of vertebrae which were caused by the global dysregulation of posterior Hox genes. The accumulation of let-7 -family microRNAs in Lin28a −/− mice resulted in the reduction of PRC1 occupancy at the Hox cluster loci by targeting Cbx2 . Consistently, Lin28a loss in embryonic stem-like cells led to aberrant induction of posterior Hox genes, which was rescued by the knockdown of let-7 -family microRNAs. These results suggest that Lin28 / let-7 pathway is possibly involved in the modulation of the “ Hox code” via Polycomb regulation during axial patterning in vertebrates.
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