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Stress‐induced lnc RNA s evade nuclear degradation and enter the translational machinery
Author(s) -
Galipon Josephine,
Miki Atsuko,
Oda Arisa,
Inada Toshifumi,
Ohta Kunihiro
Publication year - 2013
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1111/gtc.12042
Subject(s) - biology , microbiology and biotechnology , rna , degradation (telecommunications) , biochemistry , engineering , gene , telecommunications
Long noncoding RNAs (lncRNAs) play important roles in the regulation of gene expression. In fission yeast, glucose starvation triggers a transcriptional cascade of polyadenylated lncRNAs in the upstream region of the fructose‐1,6‐bisphosphatase gene ( fbp1 + ), which is correlated with stepwise chromatin remodeling and necessary for the massive induction of fbp1 + mRNA . Here, we show that these novel metabolic stress‐induced lncRNAs (mlonRNAs) are 5′‐capped, less stable than fbp1 + mRNA and sensitive to a certain extent to the nuclear exosome cofactor Rrp6. However, most mlonRNAs seem to escape nuclear degradation and are exported to the cytoplasm, where they localize to polysomes precisely during glucose starvation‐induced global translation inhibition. It is likely that ribosomes tend to accumulate in the upstream region of mlonRNAs. Although mlonRNAs contain an unusual amount of upstream AUGs ( uAUG s) and small open reading frames ( uORF s), they escape Upf1‐mediated targeting to the non‐sense‐mediated decay (NMD) pathway. The deletion of Upf1 had no effect on mlonRNA stability, but considerably destabilized fbp1 + mRNA , hinting toward a possible novel role of Upf1. Our findings suggest that the stability of mlonRNAs is distinctly regulated from mRNA and previously described noncoding transcripts.