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Identification and requirements of enhancers that direct gene expression during zebrafish fin regeneration.
Thompson, John D; Ou, Jianhong; Lee, Nutishia; Shin, Kwangdeok; Cigliola, Valentina; Song, Lingyun; Crawford, Gregory E; Kang, Junsu; Poss, Kenneth D.
  • Thompson JD; Regeneration Next, Duke University, Durham, NC 27710, USA.
  • Ou J; Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
  • Lee N; Regeneration Next, Duke University, Durham, NC 27710, USA.
  • Shin K; Regeneration Next, Duke University, Durham, NC 27710, USA.
  • Cigliola V; Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
  • Song L; Department of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53705, USA.
  • Crawford GE; Regeneration Next, Duke University, Durham, NC 27710, USA.
  • Kang J; Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
  • Poss KD; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center; Center for Genomic and Computational Biology; Center for Advanced Genomic Technologies, Durham, NC 27710, USA.
Development ; 147(14)2020 07 30.
Article en En | MEDLINE | ID: mdl-32665240
To identify candidate tissue regeneration enhancer elements (TREEs) important for zebrafish fin regeneration, we performed ATAC-seq from bulk tissue or purified fibroblasts of uninjured and regenerating caudal fins. We identified tens of thousands of DNA regions from each sample type with dynamic accessibility during regeneration, and assigned these regions to proximal genes with corresponding expression changes by RNA-seq. To determine whether these profiles reveal bona fide TREEs, we tested the sufficiency and requirements of several sequences in stable transgenic lines and mutant lines with homozygous deletions. These experiments validated new non-coding regulatory sequences near induced and/or essential genes during fin regeneration, including fgf20a, mdka and cx43, identifying distinct domains of directed expression for each confirmed TREE. Whereas deletion of the previously identified LEN enhancer abolished detectable induction of the nearby leptin b gene during regeneration, deletions of enhancers linked to fgf20a, mdka and cx43 had no effect or partially reduced gene expression. Our study generates a new resource for dissecting the regulatory mechanisms of appendage generation and reveals a range of requirements for individual TREEs in control of regeneration programs.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Regeneración / Pez Cebra / Elementos de Facilitación Genéticos / Aletas de Animales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Regeneración / Pez Cebra / Elementos de Facilitación Genéticos / Aletas de Animales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Año: 2020 Tipo del documento: Article