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Damage-responsive, maturity-silenced enhancers regulate multiple genes that direct regeneration in Drosophila.


ABSTRACT: Like tissues of many organisms, Drosophila imaginal discs lose the ability to regenerate as they mature. This loss of regenerative capacity coincides with reduced damage-responsive expression of multiple genes needed for regeneration. We previously showed that two such genes, wg and Wnt6, are regulated by a single damage-responsive enhancer that becomes progressively inactivated via Polycomb-mediated silencing as discs mature (Harris et al., 2016). Here we explore the generality of this mechanism and identify additional damage-responsive, maturity-silenced (DRMS) enhancers, some near genes known to be required for regeneration such as Mmp1, and others near genes that we now show function in regeneration. Using a novel GAL4-independent ablation system we characterize two DRMS-associated genes, apontic (apt), which curtails regeneration and CG9752/asperous (aspr), which promotes it. This mechanism of suppressing regeneration by silencing damage-responsive enhancers at multiple loci can be partially overcome by reducing activity of the chromatin regulator extra sex combs (esc).

SUBMITTER: Harris RE 

PROVIDER: S-EPMC7299344 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Damage-responsive, maturity-silenced enhancers regulate multiple genes that direct regeneration in <i>Drosophila</i>.

Harris Robin E RE   Stinchfield Michael J MJ   Nystrom Spencer L SL   McKay Daniel J DJ   Hariharan Iswar K IK  

eLife 20200603


Like tissues of many organisms, <i>Drosophila</i> imaginal discs lose the ability to regenerate as they mature. This loss of regenerative capacity coincides with reduced damage-responsive expression of multiple genes needed for regeneration. We previously showed that two such genes, <i>wg</i> and <i>Wnt6</i>, are regulated by a single damage-responsive enhancer that becomes progressively inactivated via Polycomb-mediated silencing as discs mature (Harris et al., 2016). Here we explore the genera  ...[more]

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