AAA plus Proteins RUVBL1 and RUVBL2 Coordinate PIKK Activity and Function in Nonsense-Mediated mRNA Decay

被引:125
作者
Izumi, Natsuko [1 ]
Yamashita, Akio [1 ,2 ,6 ]
Iwamatsu, Akihiro [3 ]
Kurata, Rie [1 ]
Nakamura, Hiroki [4 ]
Saari, Bonnie [5 ]
Hirano, Hisashi [4 ]
Anderson, Philip [5 ]
Ohno, Shigeo [1 ,6 ]
机构
[1] Yokohama City Univ, Sch Med, Dept Mol Biol, Yokohama, Kanagawa 2360004, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
[3] Prot Res Network Co Ltd, Yokohama, Kanagawa 2360004, Japan
[4] Yokohama City Univ, Int Grad Sch Arts & Sci, Yokohama, Kanagawa 2300045, Japan
[5] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
[6] Yokohama City Univ, Adv Med Res Ctr, Yokohama, Kanagawa 2360004, Japan
关键词
SURVEILLANCE COMPLEX; HISTONE ACETYLATION; HUMAN SMG-1; DNA-DAMAGE; C-MYC; CHROMATIN; PHOSPHORYLATION; CHAPERONE; HELICASE; REPAIR;
D O I
10.1126/scisignal.2000468
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phosphatidylinositol 3-kinase-related protein kinase (PIKK) family proteins play essential roles in DNA-based and RNA-based processes, such as the response to DNA damage, messenger RNA (mRNA) quality control, transcription, and translation, where they contribute to the maintenance of genome integrity and accurate gene expression. The adenosine triphosphatases associated with diverse cellular activities (AAA+) family proteins RuvB-like 1 (RUVBL1) and RUVBL2 are involved in various cellular processes, including transcription, RNA modification, DNA repair, and telomere maintenance. We show that RUVBL1 and RUVBL2 associate with each PIKK family member. We also show that RUVBL1 and RUVBL2 control PIKK abundance at least at the mRNA level. Knockdown of RUVBL1 or RUVBL2 decreased PIKK abundance and impaired PIKK-mediated signaling. Analysis of SMG-1, a PIKK family member involved in nonsense-mediated mRNA decay (NMD), revealed an essential role for RUVBL1 and RUVBL2 in NMD. RUVBL1 and RUVBL2 associated with SMG-1 and the messenger ribonucleoproteins in the cytoplasm and promoted the formation of mRNA surveillance complexes during NMD. Thus, RUVBL1 and RUVBL2 regulate PIKK functions on two different levels: They control the abundance of PIKKs and they stimulate the formation of PIKK-containing molecular complexes, such as those involved in NMD.
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页数:13
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