Short internal open reading frames regulate the translation of N-terminally truncated proteoforms

Fettig, R.; Gonda, Z.; Walter, N.; Sallmann, P.; Thanisch, C.; Winter, M.; Bauer, S.; Zhang, L.; Linden, G.; Litfin, M.; Etard, C.; Armant, O.; Vazquez, O.; Kassel, O.

doi:10.1101/2023.11.09.566418

bioRxiv · 10.1101/2023.11.09.566418

Short internal open reading frames regulate the translation of N-terminally truncated proteoforms

Fettig, R.·Gonda, Z.·Walter, N.·Sallmann, P.·Thanisch, C.·Winter, M.·Bauer, S.·Zhang, L.·Linden, G.·Litfin, M.·Etard, C.·Armant, O.·Vazquez, O.·Kassel, O.

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Abstract

Internal translation initiation sites, as revealed by ribosome profiling experiments can potentially drive the translation of many N-terminally truncated proteoforms. We have identified an mRNA cis-regulatory element which regulates their translation. nTRIP6 represents a short nuclear proteoform of the cytoplasmic protein TRIP6. We have previously reported that nTRIP6 regulates the dynamics of skeletal muscle progenitor differentiation. Here we show that nTRIP6 is generated by translation initiation at an internal AUG. Its translation is repressed by an internal short open reading frame (sORF) immediately upstream of the nTRIP6 AUG. Consistent with this representing a more general regulatory feature, we have identified other N-terminally truncated proteoforms which are repressed by internal sORFs. In an in vitro model of myogenic differentiation, the translation of nTRIP6 is transiently de-repressed in a mechanistic Target of Rapamycin Complex 1-dependent manner. Thus, the translation of N-terminally truncated proteoforms can be regulated independently of the canonical ORF.

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Fettig, R., Gonda, Z., Walter, N., Sallmann, P., Thanisch, C., Winter, M., Bauer, S., Zhang, L., Linden, G., Litfin, M., Etard, C., Armant, O., Vazquez, O., Kassel, O.. 2023-11-09. Short internal open reading frames regulate the translation of N-terminally truncated proteoforms. https://doi.org/10.1101/2023.11.09.566418

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