Contributions of Trf4p- and Trf5p-dependent polyadenylation to the processing and degradative functions of the yeast nuclear exosome

被引:94
作者
Egecioglu, DE
Henras, AK
Chanfreau, GF
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
Rrp6p; Rnt1p; RNase III; polyadenylation; processing; exosome;
D O I
10.1261/rna.2207206
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
The nuclear exosome is involved in a large number of RNA processing and surveillance pathways. RNase III cleavage intermediates destined to be 3'-processed or degraded can be detected when the Rrp6p subunit of the nuclear exosome is absent. Here we show that these processing and degradation intermediates are polyadenylated, and that their polyadenylation is dependent on the activity of Trf4p and Trf5p, two variant poly(A) polymerases. Polyadenylation of cleavage intermediates was inhibited when Trf4p was absent, and reduced to various extents in the absence of Trf5p, suggesting that these two poly(A) polymerases play functionally distinct roles in the polyadenylation of these RNA species. Finally, in the absence of Trf4p, we observed 3'-extended forms of the U4 snRNA that are similar to those observed in the absence of Rrp6p. These results suggest that polyadenylation of RNA processing intermediates plays a functional role in RNA processing pathways and is not limited to RNA surveillance functions.
引用
收藏
页码:26 / 32
页数:7
相关论文
共 23 条
[1]   RNase III cleaves eukaryotic preribosomal RNA at a U3 snoRNP-dependent site [J].
AbouElela, S ;
Igel, H ;
Ares, M .
CELL, 1996, 85 (01) :115-124
[2]   Functions of the exosome in rRNA, snoRNA and snRNA synthesis [J].
Allmang, C ;
Kufel, J ;
Chanfreau, G ;
Mitchell, P ;
Petfalski, E ;
Tollervey, D .
EMBO JOURNAL, 1999, 18 (19) :5399-5410
[3]   A SIMPLE AND EFFICIENT METHOD FOR DIRECT GENE DELETION IN SACCHAROMYCES-CEREVISIAE [J].
BAUDIN, A ;
OZIERKALOGEROPOULOS, O ;
DENOUEL, A ;
LACROUTE, F ;
CULLIN, C .
NUCLEIC ACIDS RESEARCH, 1993, 21 (14) :3329-3330
[4]   Identification of a regulated pathway for nuclear pre-mRNA turnover [J].
Bousquet-Antonelli, C ;
Presutti, C ;
Tollervey, D .
CELL, 2000, 102 (06) :765-775
[5]   Alternative 3'-end processing of U5 snRNA by RNase III [J].
Chanfreau, G ;
AbouElela, S ;
Ares, M ;
Guthrie, C .
GENES & DEVELOPMENT, 1997, 11 (20) :2741-2751
[6]   Yeast RNase III as a key processing enzyme in small nucleolar RNAs metabolism [J].
Chanfreau, G ;
Legrain, P ;
Jacquier, A .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 284 (04) :975-988
[7]   Processing of a dicistronic small nucleolar RNA precursor by the RNA endonuclease Rnt1 [J].
Chanfreau, G ;
Rotondo, G ;
Legrain, P ;
Jacquier, A .
EMBO JOURNAL, 1998, 17 (13) :3726-3737
[8]   RNAse III-mediated degradation of unspliced pre-mRNAs and lariat introns [J].
Danin-Kreiselman, M ;
Lee, CY ;
Chanfreau, G .
MOLECULAR CELL, 2003, 11 (05) :1279-1289
[9]   Depletion of yeast RNase III blocks correct U2 3′ end formation and results in polyadenylated but functional U2 snRNA [J].
Elela, SA ;
Ares, M .
EMBO JOURNAL, 1998, 17 (13) :3738-3746
[10]   Trf4 and trf5 proteins of Saccharomyces cerevisiae exhibit poly(A) RNA polymerase activity but no DNA polymerase activity [J].
Haracska, L ;
Johnson, RE ;
Prakash, L ;
Prakash, S .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (22) :10183-10189