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The Lin28/let-7 Pathway Regulates the Mammalian Caudal Body Axis Elongation Program.
Robinton, Daisy A; Chal, Jérome; Lummertz da Rocha, Edroaldo; Han, Areum; Yermalovich, Alena V; Oginuma, Masayuki; Schlaeger, Thorsten M; Sousa, Patricia; Rodriguez, Antony; Urbach, Achia; Pourquié, Olivier; Daley, George Q.
Affiliation
  • Robinton DA; Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Howard Hughes Medical Institute, Boston, MA 02115, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA
  • Chal J; Harvard Stem Cell Institute, Boston, MA 02115, USA; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Lummertz da Rocha E; Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA 02115, USA.
  • Han A; Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Howard Hughes Medical Institute, Boston, MA 02115, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA
  • Yermalovich AV; Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Howard Hughes Medical Institute, Boston, MA 02115, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA
  • Oginuma M; Harvard Stem Cell Institute, Boston, MA 02115, USA; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Schlaeger TM; Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA 02115, USA.
  • Sousa P; Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Howard Hughes Medical Institute, Boston, MA 02115, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA
  • Rodriguez A; Department of Medicine, Immunology, Allergy and Rheumatology, Baylor College of Medicine, Houston, TX 77030, USA.
  • Urbach A; Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel.
  • Pourquié O; Harvard Stem Cell Institute, Boston, MA 02115, USA; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Daley GQ; Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Howard Hughes Medical Institute, Boston, MA 02115, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA
Dev Cell ; 48(3): 396-405.e3, 2019 02 11.
Article in En | MEDLINE | ID: mdl-30661985
The heterochronic genes Lin28a/b and let-7 regulate invertebrate development, but their functions in patterning the mammalian body plan remain unexplored. Here, we describe how Lin28/let-7 influence caudal vertebrae number during body axis formation. We found that FoxD1-driven overexpression of Lin28a strikingly increased caudal vertebrae number and tail bud cell proliferation, whereas its knockout did the opposite. Lin28a overexpression downregulated the neural marker Sox2, causing a pro-mesodermal phenotype with a decreased proportion of neural tissue relative to nascent mesoderm. Manipulating Lin28a and let-7 led to opposite effects, and manipulating Lin28a's paralog, LIN28B caused similar yet distinct phenotypes. These findings suggest that Lin28/let-7 play a role in the regulation of tail length through heterochrony of the body plan. We propose that the Lin28/let-7 pathway controls the pool of caudal progenitors during tail development, promoting their self-renewal and balancing neural versus mesodermal cell fate decisions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA-Binding Proteins / MicroRNAs / Morphogenesis Type of study: Prognostic_studies Limits: Animals Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2019 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA-Binding Proteins / MicroRNAs / Morphogenesis Type of study: Prognostic_studies Limits: Animals Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2019 Type: Article