VT1102 |
lin-28(n719) I; lin-46(ma164) nDf51 V; mir-84(n4037) X. |
C. elegans |
Strong retarded heterochronic phenotype, reiteration of L2-stage program resulting in extra seam cells and failure to generate alae. nDf51 is a 5930 bp deletion starting 1762 bp upstream of mir-241, removing mir-241, mir-48, and F56A12.6 (snoRNA). |
VT1145 |
lin-46(ma164) nDf51 V; mir-84(n4037) X. |
C. elegans |
Strong retarded heterochronic phenotype, reiteration of L2-stage program resulting in extra seam cells and failure to generate alae. Vul. nDf51 is a 5930 bp deletion starting 1762 bp upstream of mir-241, removing mir-241, mir-48, and F56A12.6 (snoRNA). |
VT581 |
dpy-5(e61) lin-28(n719) I; lin-46(ma164) unc-76(e911) V. |
C. elegans |
Dpy Unc. Egl+. lin-46 suppresses precocious Egl- phenotype of lin-28. lin-46 alone makes gaps in adult alae; enhanced at 15C. |