作者
Ruorong Yan,Valentina Cigliola,Kelsey A. Oonk,Zachary Petrover,Sophia DeLuca,David Wolfson,Andrew M. Vekstein,Michelle Mendiola,Garth Devlin,Muath Bishawi,Matthew Gemberling,Tanvi Sinha,Michelle A. Sargent,Allen J. York,Avraham Shakked,Paige DeBenedittis,David C. Wendell,Jianhong Ou,Junsu Kang,Joseph Goldman,Gurpreet S. Baht,Ravi Karra,Adam Williams,Dawn E. Bowles,Aravind Asokan,Eldad Tzahor,Charles A. Gersbach,Jeffery D Molkentin,Nenad Bursac,Brian L. Black,Kenneth D. Poss
摘要
The efficacy and safety of gene-therapy strategies for indications like tissue damage hinge on precision; yet, current methods afford little spatial or temporal control of payload delivery. Here, we find that tissue-regeneration enhancer elements (TREEs) isolated from zebrafish can direct targeted, injury-associated gene expression from viral DNA vectors delivered systemically in small and large adult mammalian species. When employed in combination with CRISPR-based epigenome editing tools in mice, zebrafish TREEs stimulated or repressed the expression of endogenous genes after ischemic myocardial infarction. Intravenously delivered recombinant AAV vectors designed with a TREE to direct a constitutively active YAP factor boosted indicators of cardiac regeneration in mice and improved the function of the injured heart. Our findings establish the application of contextual enhancer elements as a potential therapeutic platform for spatiotemporally controlled tissue regeneration in mammals.