TY - JOUR
T1 - XMtr4-like protein coordinates nuclear RNA processing for heterochromatin assembly and for telomere maintenance
AU - Lee, Nathan N.
AU - Chalamcharla, Venkata R.
AU - Reyes-Turcu, Francisca
AU - Mehta, Sameet
AU - Zofall, Martin
AU - Balachandran, Vanivilasini
AU - Dhakshnamoorthy, Jothy
AU - Taneja, Nitika
AU - Yamanaka, Soichiro
AU - Zhou, Ming
AU - Grewal, Shiv I.S.
N1 - Funding Information:
We thank P. FitzGerald for intron analysis, R. Allshire for the cwf10-1 mutant, J. Barrowman for her valuable help in editing the manuscript, and M. Lichten for comments. This research was supported by the Intramural Research Program of the National Institutes of Health (NIH) and by the National Cancer Institute and utilized the Helix Systems and the Biowulf Linux cluster at the NIH.
PY - 2013/11/21
Y1 - 2013/11/21
N2 - The regulation of protein-coding and noncoding RNAs is linked to nuclear processes, including chromatin modifications and gene silencing. However, the mechanisms that distinguish RNAs and mediate their functions are poorly understood. We describe a nuclear RNA-processing network in fission yeast with a core module comprising the Mtr4-like protein, Mtl1, and the zinc-finger protein, Red1. The Mtl1-Red1 core promotes degradation of mRNAs and noncoding RNAs and associates with different proteins to assemble heterochromatin via distinct mechanisms. Mtl1 also forms Red1-independent interactions with evolutionarily conserved proteins named Nrl1 and Ctr1, which associate with splicing factors. Whereas Nrl1 targets transcripts with cryptic introns to form heterochromatin at developmental genes and retrotransposons, Ctr1 functions in processing intron-containing telomerase RNA. Together with our discovery of widespread cryptic introns, including in noncoding RNAs, these findings reveal unique cellular strategies for recognizing regulatory RNAs and coordinating their functions in response to developmental and environmental cues.
AB - The regulation of protein-coding and noncoding RNAs is linked to nuclear processes, including chromatin modifications and gene silencing. However, the mechanisms that distinguish RNAs and mediate their functions are poorly understood. We describe a nuclear RNA-processing network in fission yeast with a core module comprising the Mtr4-like protein, Mtl1, and the zinc-finger protein, Red1. The Mtl1-Red1 core promotes degradation of mRNAs and noncoding RNAs and associates with different proteins to assemble heterochromatin via distinct mechanisms. Mtl1 also forms Red1-independent interactions with evolutionarily conserved proteins named Nrl1 and Ctr1, which associate with splicing factors. Whereas Nrl1 targets transcripts with cryptic introns to form heterochromatin at developmental genes and retrotransposons, Ctr1 functions in processing intron-containing telomerase RNA. Together with our discovery of widespread cryptic introns, including in noncoding RNAs, these findings reveal unique cellular strategies for recognizing regulatory RNAs and coordinating their functions in response to developmental and environmental cues.
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U2 - 10.1016/j.cell.2013.10.027
DO - 10.1016/j.cell.2013.10.027
M3 - Article
C2 - 24210919
AN - SCOPUS:84889599430
SN - 0092-8674
VL - 155
SP - 1061
JO - Cell
JF - Cell
IS - 5
ER -