An increased ratio of eif4e1c to canonical cap binding alleles improves heart regeneration. (A) Hearts, 7 days after amputation of the apex and after 3 days injection of EdU. CM are stained with α-Mef2c. (B) The single Δeif4ea mutants (green) and the Δeif4eb mutants (purple) have increased levels of CM proliferation (Mean: wildtype = 9.6%, Δeif4ea = 12.9%, Δeif4eb = 12.8%, Δeif4ea/Δeif4eb = 8.1%, ANOVA p < 0.0001, N = 48, 37, 40, 38). However, after a certain threshold, eif4e1c fully compensates since Δeif4ea/Δeif4ea double mutants (pink) regenerate like their wildtype (black) siblings. (C) Graph of fin regrowth 2 days post amputation in the respective mutants (Mean: wildtype = 244um, Δeif4ea/Δeif4eb = 270um, Δeif4ea = 194um, Δeif4eb = 183um, ANOVA p-value <0.0001, N = 50, 73, 41, 42). (D) Images of representative fins from the graph. Error bars representmean ± s.e.m. Scale bar = 100um. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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