Cargando…

Lin28, a major translation reprogramming factor, gains access to YB-1-packaged mRNA through its cold-shock domain

The RNA-binding protein Lin28 (Lin28a) is an important pluripotency factor that reprograms translation and promotes cancer progression. Although Lin28 blocks let-7 microRNA maturation, Lin28 also binds to a large set of cytoplasmic mRNAs directly. However, how Lin28 regulates the processing of many...

Descripción completa

Detalles Bibliográficos
Autores principales: Samsonova, Anastasiia, El Hage, Krystel, Desforges, Bénédicte, Joshi, Vandana, Clément, Marie-Jeanne, Lambert, Guillaume, Henrie, Hélène, Babault, Nicolas, Craveur, Pierrick, Maroun, Rachid C., Steiner, Emilie, Bouhss, Ahmed, Maucuer, Alexandre, Lyabin, Dmitry N., Ovchinnikov, Lev P., Hamon, Loic, Pastré, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979924/
https://www.ncbi.nlm.nih.gov/pubmed/33742080
http://dx.doi.org/10.1038/s42003-021-01862-3
Descripción
Sumario:The RNA-binding protein Lin28 (Lin28a) is an important pluripotency factor that reprograms translation and promotes cancer progression. Although Lin28 blocks let-7 microRNA maturation, Lin28 also binds to a large set of cytoplasmic mRNAs directly. However, how Lin28 regulates the processing of many mRNAs to reprogram global translation remains unknown. We show here, using a structural and cellular approach, a mixing of Lin28 with YB-1 (YBX1) in the presence of mRNA owing to their cold-shock domain, a conserved β-barrel structure that binds to ssRNA cooperatively. In contrast, the other RNA binding-proteins without cold-shock domains tested, HuR, G3BP-1, FUS and LARP-6, did not mix with YB-1. Given that YB-1 is the core component of dormant mRNPs, a model in which Lin28 gains access to mRNPs through its co-association with YB-1 to mRNA may provide a means for Lin28 to reprogram translation. We anticipate that the translational plasticity provided by mRNPs may contribute to Lin28 functions in development and adaptation of cancer cells to an adverse environment.