The C. elegans microRNA let-7 binds to imperfect let-7 complementary sites from the lin-41 3′ UTR

MC Vella, EY Choi, SY Lin, K Reinert… - Genes & …, 2004 - genesdev.cshlp.org
MC Vella, EY Choi, SY Lin, K Reinert, FJ Slack
Genes & development, 2004genesdev.cshlp.org
Caenorhabditis elegans let-7, a founding member of the microRNA family, is predicted to
bind to six sites in the 3′ UTR of the mRNA of its target gene, lin-41, to down-regulate LIN-
41. Here, we demonstrate that wild-type let-7 microRNA binds in vitro to RNA from the lin-41
3′ UTR. This interaction is dependent on two conserved let-7 complementary sites (LCSs).
A 27-nucleotide sequence between the LCSs is also necessary for down-regulation in vivo.
LCS mutations compensatory to the lesion in let-7 (n2853) can partially restore lin-41 3 …
Caenorhabditis elegans let-7, a founding member of the microRNA family, is predicted to bind to six sites in the 3′UTR of the mRNA of its target gene, lin-41, to down-regulate LIN-41. Here, we demonstrate that wild-type let-7 microRNA binds in vitro to RNA from the lin-41 3′UTR. This interaction is dependent on two conserved let-7 complementary sites (LCSs). A 27-nucleotide sequence between the LCSs is also necessary for down-regulation in vivo. LCS mutations compensatory to the lesion in let-7(n2853) can partially restore lin-41 3′UTR function in a let-7(n2853) background, providing the first experimental evidence for an animal miRNA binding directly to its validated target in vivo.
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