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A screen for regeneration-associated silencer regulatory elements in zebrafish.
Ando, Kazunori; Ou, Jianhong; Thompson, John D; Welsby, John; Bangru, Sushant; Shen, Jingwen; Wei, Xiaolin; Diao, Yarui; Poss, Kenneth D.
Afiliação
  • Ando K; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Ou J; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Thompson JD; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Welsby J; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Bangru S; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Shen J; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Wei X; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Diao Y; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Poss KD; Duke Regeneration Center and Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA. Electronic address: ken.poss@duke.edu.
Dev Cell ; 59(5): 676-691.e5, 2024 Mar 11.
Article em En | MEDLINE | ID: mdl-38290519
ABSTRACT
Regeneration involves gene expression changes explained in part by context-dependent recruitment of transcriptional activators to distal enhancers. Silencers that engage repressive transcriptional complexes are less studied than enhancers and more technically challenging to validate, but they potentially have profound biological importance for regeneration. Here, we identified candidate silencers through a screening process that examined the ability of DNA sequences to limit injury-induced gene expression in larval zebrafish after fin amputation. A short sequence (s1) on chromosome 5 near several genes that reduce expression during adult fin regeneration could suppress promoter activity in stable transgenic lines and diminish nearby gene expression in knockin lines. High-resolution analysis of chromatin organization identified physical associations of s1 with gene promoters occurring preferentially during fin regeneration, and genomic deletion of s1 elevated the expression of these genes after fin amputation. Our study provides methods to identify "tissue regeneration silencer elements" (TRSEs) with the potential to reduce unnecessary or deleterious gene expression during regeneration.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Elementos Silenciadores Transcricionais Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Elementos Silenciadores Transcricionais Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article