Regulation of NAB2 mRNA 3′-end formation requires the core exosome and the Trf4p component of the TRAMP complex

被引:20
作者
Roth, Kelly M. [1 ]
Byam, Joel [1 ]
Fang, Feng [1 ]
Butler, J. Scott [1 ]
机构
[1] Univ Rochester, Dept Microbiol & Immunol, Sch Med & Dent, Med Ctr, Rochester, NY 14642 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
RNA processing; TRAMP complex; exosome; mRNA 3 '-end formation; TAIL LENGTH CONTROL; YEAST NUCLEAR EXOSOME; 3' END FORMATION; HUMAN PM-SCL; SACCHAROMYCES-CEREVISIAE; QUALITY-CONTROL; POLY(A) POLYMERASE; TRANSCRIPTION TERMINATION; RIBOSOMAL-RNA; POLYADENYLATION FACTOR;
D O I
10.1261/rna.709609
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 functions in a variety of pathways catalyzing formation of mature RNA 3'-ends or the destruction of aberrant RNA transcripts. The RNA 3'-end formation activity of the exosome appeared restricted to small noncoding RNAs. However, the nuclear exosome controls the level of the mRNA encoding the poly( A)- binding protein Nab2p in a manner requiring an A(26) sequence in the mRNA 39 untranslated regions (UTR), and the activities of Nab2p and the exosome-associated exoribonuclease Rrp6p. Here we show that the A26 sequence inhibits normal 3'-end processing of NAB2 mRNA in vivo and in vitro, and makes formation of the mature 3'-end dependent on trimming of the transcript by the core exosome and the Trf4p component of the TRAMP complex from a downstream site. The detection of mature, polyadenylated transcripts ending at, or within, the A26 sequence indicates that exosome trimming sometimes gives way to polyadenylation of the mRNA. Alternatively, Rrp6p and the TRAMP-associated Mtr4p degrade these transcripts thereby limiting the amount of Nab2p in the cell. These findings suggest that NAB2 mRNA 3'-end formation requires the exosome and TRAMP complex, and that competition between polyadenylation and Rrp6p-dependent degradation controls the level of this mRNA.
引用
收藏
页码:1045 / 1058
页数:14
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