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A B1 SINE element within the mouse Malat1 long noncoding RNA acts as an internal ribosome entry site mediating micropeptide translation.
Science Advances · · Journal Article
Xiao, Hann + more
Abstract ↗AI summary
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A B1 SINE element within mouse Malat1 acts as an IRES that enables cap-independent translation of the M1 micropeptide in neurons.
- Why it matters: Understanding how noncoding RNAs like Malat1 can produce functional peptides challenges the traditional view of their roles and may reveal new mechanisms of gene regulation in cells.
- What they did: The researchers used in vivo chemical probing, structural modeling, and affinity purification to identify a three-stem-loop IRES structure overlapping a B1 SINE element that binds ribosomal and translation factors, and they showed that depletion of specific cofactors inhibits M1 translation.
- The result: This work uncovers a hidden functional unit within Malat1 that facilitates micropeptide production, suggesting that some long noncoding RNAs may have coding potential through embedded IRES elements.
The findingWhy it mattersWhat they didThe result