Biology, asked by Geethika79361, 10 months ago

In
c. Elegans, loss-of-function alleles of the skn-1+ gene cause ems to be re-specified as
c. Skn-1+ mrna is present in all cells of the early embryo. However, very little protein is made in abx cells. How is this possible? What does a loss of function mutation in mex-1 look like?

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Answered by tannu3144
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