Lin28a/let-7 pathway modulates the Hox code via Polycomb regulation during axial patterning in vertebrates

Author:

Sato Tempei123ORCID,Kataoka Kensuke13,Ito Yoshiaki14,Yokoyama Shigetoshi25ORCID,Inui Masafumi26ORCID,Mori Masaki17,Takahashi Satoru8,Akita Keiichi9ORCID,Takada Shuji2,Ueno-Kudoh Hiroe210,Asahara Hiroshi121112ORCID

Affiliation:

1. Department of Systems BioMedicine, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan

2. Department of Systems BioMedicine, National Research Institute for Child Health and Development, Tokyo, Japan

3. Research Fellow of Japan Society for the Promotion of Science, Tokyo, Japan

4. Research Core, Tokyo Medical and Dental University, Tokyo, Japan

5. Laboratory of Metabolism, National Institutes of Health, Bethesda, United States

6. Laboratory of Animal Regeneration Systemology, Meiji University, Kanagawa, Japan

7. Department of Medical Chemistry, Shiga University of Medical Science, Shiga, Japan

8. Department of Anatomy and Embryology, University of Tsukuba, Ibaraki, Japan

9. Department of Clinical Anatomy, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan

10. Reproduction Center, Yokohama City University, Yokohama, Japan

11. AMED-CREST, Japan Agency for Medical Research and Development (AMED), Tokyo, Japan

12. Department of Molecular Medicine, The Scripps Research Institute, La Jolla, United States

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 pathway is critical for axial elongation. Lin28a–/– mice exhibited axial shortening with mild skeletal transformations of vertebrae, which were consistent with results in mice with tail bud-specific mutants of Lin28a. The accumulation of let-7 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. These results suggest that the Lin28/let-7 pathway is involved in the modulation of the ‘Hox code’ via Polycomb regulation during axial patterning.

Funder

Japan Agency for Medical Research and Development

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Japan Society for the Promotion of Science

Core Research for Evolutional Science and Technology

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference113 articles.

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5. Targeted disruption of Hoxd-10 affects mouse hindlimb development;Carpenter;Development,1997

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