MiR-71 regulates vulval cell division during recovery of starved L1 worms. We thus asked whether miR-71 was required for the reinitiation of developmental programs during the recovery phase after L1 starvation. These results indicate that miR-71 is not essential for arresting seam cell or M-cell divisions during L1 diapause, suggesting that miR-71 function is distinct from DAF-16 function. DAF-16 (the FOXO homolog in C. elegans) has been shown to play an important role in cell cycle arrest and developmental progression partly by promoting cki-1 expression in some somatic cells during L1 arrest (2). S1A indicated a dominant role of intestinal miRNAs in regulating L1 starvation survival.
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