| Literature DB >> 12757712 |
Ibrahim Yaman1, James Fernandez, Haiyan Liu, Mark Caprara, Anton A Komar, Antonis E Koromilas, Lingyin Zhou, Martin D Snider, Donalyn Scheuner, Randal J Kaufman, Maria Hatzoglou.
Abstract
Transport of the essential amino acids arginine and lysine is critical for the survival of mammalian cells. The adaptive response to nutritional stress involves increased translation of the arginine/lysine transporter (cat-1) mRNA via an internal ribosome entry site (IRES) within the mRNA leader. Induction of cat-1 IRES activity requires both translation of a small upstream open reading frame (uORF) within the IRES and phosphorylation of the translation initiation factor eIF2alpha. We show here that translation of the upstream ORF unfolds an inhibitory structure in the mRNA leader, eliciting a conformational change that yields an active IRES. The IRES, whose activity is induced by amino acid starvation, is created by RNA-RNA interactions between the 5' end of the leader and downstream sequences. This study suggests that the structure of the IRES is dynamic and regulation of this RNA structure is a mechanism of translational control.Entities:
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Year: 2003 PMID: 12757712 DOI: 10.1016/s0092-8674(03)00345-3
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582