Perlman syndrome nuclease DIS3L2 controls cytoplasmic non-coding RNAs and provides surveillance pathway for maturing snRNAs.
Perlman syndrome nuclease DIS3L2 controls cytoplasmic non-coding RNAs and provides surveillance pathway for maturing snRNAs.
复制标题
DOI:
10.1093/nar/gkw649
复制
发表时间:
2016-12-01
影响因子:
14.9
通讯作者:
Dziembowski A
中科院分区:
文献类型:
--
作者:
Łabno A;Warkocki Z;Kuliński T;Krawczyk PS;Bijata K;Tomecki R;Dziembowski A
The exosome-independent exoribonuclease DIS3L2 is mutated in Perlman syndrome. Here, we used extensive global transcriptomic and targeted biochemical analyses to identify novel DIS3L2 substrates in human cells. We show that DIS3L2 regulates pol II transcripts, comprising selected canonical and histone-coding mRNAs, and a novel FTL_short RNA from the ferritin mRNA 5′ UTR. Importantly, DIS3L2 contributes to surveillance of maturing snRNAs during their cytoplasmic processing. Among pol III transcripts, DIS3L2 particularly targets vault and Y RNAs and an Alu-like element BC200 RNA, but not Alu repeats, which are removed by exosome-associated DIS3. Using 3′ RACE-Seq, we demonstrate that all novel DIS3L2 substrates are uridylated in vivo by TUT4/TUT7 poly(U) polymerases. Uridylation-dependent DIS3L2-mediated decay can be recapitulated in vitro, thus reinforcing the tight cooperation between DIS3L2 and TUTases. Together these results indicate that catalytically inactive DIS3L2, characteristic of Perlman syndrome, can lead to deregulation of its target RNAs to disturb transcriptome homeostasis.
登录
查看更多内容
DOI:
10.1073/pnas.84.23.8478
发表时间:
1987-12-01
影响因子:
11.1
作者:
AZIZ, N;MUNRO, HN
通讯作者:
MUNRO, HN
影响因子:
5.3
作者:
Lin, Daisy;Pestova, Tatyana V.;Tiedge, Henri
通讯作者:
Tiedge, Henri
DOI:
10.1007/978-1-4419-7841-7_8
发表时间:
2010-01-01
期刊:
RNA EXOSOME
影响因子:
--
作者:
Butler, J. Scott;Mitchell, Phil
通讯作者:
Mitchell, Phil
影响因子:
20.6
作者:
Fu XD
通讯作者:
Fu XD
影响因子:
14.8
作者:
Gagnon, Keith T.;Li, Liande;Janowski, Bethany A.;Corey, David R.
通讯作者:
Corey, David R.