4.8 Article

Modulation of tissue repair by regeneration enhancer elements

期刊

NATURE
卷 532, 期 7598, 页码 201-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/nature17644

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资金

  1. AHA [12POST11920060]
  2. NIH Clinical Investigator Award [K08 HL116485]
  3. NSF Graduate Research Fellowship [1106401]
  4. NIH [F32 HL120494, R01 HL089707, R01 HL064658, R01 GM074057, R01 HL081674]
  5. HHMI

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How tissue regeneration programs are triggered by injury has received limited research attention. Here we investigate the existence of enhancer regulatory elements that are activated in regenerating tissue. Transcriptomic analyses reveal that leptin b (lepb) is highly induced in regenerating hearts and fins of zebrafish. Epigenetic profiling identified a short DNA sequence element upstream and distal to lepb that acquires open chromatin marks during regeneration and enables injury-dependent expression from minimal promoters. This element could activate expression in injured neonatal mouse tissues and was divisible into tissue-specific modules sufficient for expression in regenerating zebrafish fins or hearts. Simple enhancer-effector transgenes employing lepb-linked sequences upstream of pro-or anti-regenerative factors controlled the efficacy of regeneration in zebrafish. Our findings provide evidence for 'tissue regeneration enhancer elements' (TREEs) that trigger gene expression in injury sites and can be engineered to modulate the regenerative potential of vertebrate organs.

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