MicroRNA-10a binds the 5'UTR of ribosomal protein mRNAs and enhances their translation.

TY - JOUR

T1 - MicroRNA-10a binds the 5'UTR of ribosomal protein mRNAs and enhances their translation.

AU - Ørom, Ulf Andersson

AU - Nielsen, Finn Cilius

AU - Lund, Anders Henrik

N1 - Keywords: 5' Untranslated Regions; Amino Acids; Animals; Base Sequence; Binding Sites; Cell Transformation, Neoplastic; Hela Cells; Humans; Membrane Glycoproteins; Mice; Molecular Sequence Data; NIH 3T3 Cells; Protein Biosynthesis; Rats; Receptors, Immunologic; Ribosomal Proteins

PY - 2008

Y1 - 2008

N2 - MicroRNAs (miRNAs) are small RNAs that function as posttranscriptional regulators of gene expression. miRNAs affect a variety of signaling pathways, and impaired miRNA regulation may contribute to the development of cancer and other diseases. Here we show that miRNA miR-10a interacts with the 5' untranslated region of mRNAs encoding ribosomal proteins to enhance their translation. miR-10a alleviates translational repression of the ribosomal protein mRNAs during amino acid starvation and is required for their translational induction following anisomycin treatment or overexpression of RAS. We show that miR-10a binds immediately downstream of the regulatory 5'TOP motif and that the 5'TOP regulatory complex and miR-10a are functionally interconnected. The results show that miR-10a may positively control global protein synthesis via the stimulation of ribosomal protein mRNA translation and ribosome biogenesis and hereby affect the ability of cells to undergo transformation.

AB - MicroRNAs (miRNAs) are small RNAs that function as posttranscriptional regulators of gene expression. miRNAs affect a variety of signaling pathways, and impaired miRNA regulation may contribute to the development of cancer and other diseases. Here we show that miRNA miR-10a interacts with the 5' untranslated region of mRNAs encoding ribosomal proteins to enhance their translation. miR-10a alleviates translational repression of the ribosomal protein mRNAs during amino acid starvation and is required for their translational induction following anisomycin treatment or overexpression of RAS. We show that miR-10a binds immediately downstream of the regulatory 5'TOP motif and that the 5'TOP regulatory complex and miR-10a are functionally interconnected. The results show that miR-10a may positively control global protein synthesis via the stimulation of ribosomal protein mRNA translation and ribosome biogenesis and hereby affect the ability of cells to undergo transformation.

U2 - 10.1016/j.molcel.2008.05.001

DO - 10.1016/j.molcel.2008.05.001

M3 - Journal article

C2 - 18498749

SN - 1097-2765

VL - 30

SP - 460

EP - 471

JO - Molecular Cell

JF - Molecular Cell

IS - 4

ER -