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Ascl1a regulates Müller glia dedifferentiation and retinal regeneration through a Lin-28-dependent, let-7 microRNA signalling pathway

A Corrigendum to this article was published on 27 March 2015

This article has been updated

Abstract

Unlike mammals, teleost fish mount a robust regenerative response to retinal injury that culminates in restoration of visual function1,2. This regenerative response relies on dedifferentiation of Müller glia into a cycling population of progenitor cells. However, the mechanism underlying this dedifferentiation is unknown. Here, we report that genes encoding pluripotency factors are induced following retinal injury. Interestingly, the proneural transcription factor, Ascl1a, and the pluripotency factor, Lin-28, are induced in Müller glia within 6 h following retinal injury and are necessary for Müller glia dedifferentiation. We demonstrate that Ascl1a is necessary for lin-28 expression and that Lin-28 suppresses let-7 microRNA (miRNA) expression. Furthermore, we demonstrate that let-7 represses expression of regeneration-associated genes such as, ascl1a, hspd1, lin-28, oct4, pax6b and c-myc. hspd1, oct4 and c-myca exhibit basal expression in the uninjured retina and let-7 may inhibit this expression to prevent premature Müller glia dedifferentiation. The opposing actions of Lin-28 and let-7 miRNAs on Müller glia differentiation and dedifferentiation are similar to that of embryonic stem cells3 and suggest novel targets for stimulating Müller glia dedifferentiation and retinal regeneration in mammals.

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Figure 1: ascl1a and lin-28 mRNAs are rapidly induced in dedifferentiating Müller glia following retinal injury.
Figure 2: Ascl1a and Lin-28 knockdown inhibit 1016 tuba1a:gfp transgene expression and Müller glia-derived progenitor proliferation.
Figure 3: Ascl1a regulates lin-28 expression.
Figure 4: Lin-28 regulates let-7 miRNA levels in Müller glia-derived progenitors.
Figure 5: let-7 miRNAs suppress expression of regeneration- and pluripotency-associated genes.

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Change history

  • 25 February 2015

    In the version of this Letter originally published the first lin-28 targeting morpholino oligonucleotide should have read: 5′-GGGCATCTTTATGATTTAGCCTTCT-3′. This has been corrected in all online versions of the Letter.

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Acknowledgements

We thank D. Hyde for sharing gfap:gfp transgenic fish, R. Thompson, D. Turner and M. Uhler for sharing expression vectors and reagents, J. Beals for help with confocal microscopy, the UM Flow Cytometry Core for help purifying GFP-labelled Müller glia, V. Kapuria for help with western blots; B. R. Wilfred and D. Turner for advice on miRNAs, P. Macpherson for help with statistics, T. Melendez for expert care of fish and D. Turner, J. Parent and members of the Goldman lab for their support and comments on this work. This work was supported by funds from the NIH NEI RO1 EY018132 (to D.G.) and NIH NICHD T32HD007507 (to R.R.).

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D.G. and R.R. designed and analyzed the research and wrote the paper. D.G. generated the 1016 tuba1a:gfp transgenic fish. R.R. performed all experiments except for Fig. 4a, e where B.V.F. assayed let-7a and let-7f miRNA levels by RT–PCR.

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Correspondence to Daniel Goldman.

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The authors declare no competing financial interests.

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Ramachandran, R., Fausett, B. & Goldman, D. Ascl1a regulates Müller glia dedifferentiation and retinal regeneration through a Lin-28-dependent, let-7 microRNA signalling pathway. Nat Cell Biol 12, 1101–1107 (2010). https://doi.org/10.1038/ncb2115

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