Localization of nuclear retained mRNAs in Saccharomyces cerevisiae

被引:61
作者
Thomsen, R
Libri, D
Boulay, J
Rosbash, M
Jensen, TH
机构
[1] Aarhus Univ, Dept Mol Biol, DK-8000 Aarhus C, Denmark
[2] CNRS, Ctr Genet Mol, F-91190 Gif Sur Yvette, France
[3] Brandeis Univ, Dept Biol, Howard Hughes Med Inst, Waltham, MA 02454 USA
关键词
nuclear mRNA retention; transcription-site foci; mRNA release; nuclear bodies;
D O I
10.1261/rna.5170303
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
In the yeast Saccharomyces cerevisiae, a common conditional phenotype associated with deletion or mutation of genes encoding mRNA export factors is the rapid accumulation of mRNAs in intranuclear foci, suggested to be near transcription sites. The nuclear RNA exosome has been implicated in retaining RNAs in these foci; on deletion of the exosome component Rrp6p, the RNA is released. To determine the exact nuclear location of retained as well as released mRNAs, we have used mRNA export mutant strains to analyze the spatial relationship between newly synthesized heat shock mRNA, the chromosomal site of transcription, and known S. cerevisiae nuclear structures such as the nucleolus and the nucleolar body. Our results show that retained SSA4 RNA localizes to an area in close proximity to the SSA4 locus. On deletion of Rrp6p and release from the genomic locus, heat shock mRNAs produced in the rat7-1 strain colocalize predominantly with nucleolar antigens. Bulk poly(A)(+) RNA, on the other hand, is localized primarily to the nuclear rim. Interestingly, the RNA binding nucleocytoplasmic shuttle protein Npl3p shows strong colocalization with bulk poly(A)(+) RNA, regardless of its nuclear location. Taken together, our data show that retention occurs close to the gene and indicate distinct nuclear fates of different mRNAs.
引用
收藏
页码:1049 / 1057
页数:9
相关论文
共 23 条
[1]   The yin and yang of the exosome [J].
Butler, JS .
TRENDS IN CELL BIOLOGY, 2002, 12 (02) :90-96
[2]   Classics in enzymology: The kinetics of the enzyme-substrate compound of peroxidase (Reprinted from Journal of Biological Chemistry, vol 151, pg 553-573, 1943) [J].
Chance, B .
ADVANCES IN ENZYMOLOGY, VOL 73, 1999, 73 :1-+
[3]   The yeast HPR1 gene has a functional role in transcriptional elongation that uncovers a novel source of genome instability [J].
Chávez, S ;
Aguilera, A .
GENES & DEVELOPMENT, 1997, 11 (24) :3459-3470
[4]   An ESP1/PDS1 complex regulates loss of sister chromatid cohesion at the metaphase to anaphase transition in yeast [J].
Ciosk, R ;
Zachariae, W ;
Michaelis, C ;
Shevchenko, A ;
Mann, M ;
Nasmyth, K .
CELL, 1998, 93 (06) :1067-1076
[5]   A YEAST RNA-BINDING PROTEIN SHUTTLES BETWEEN THE NUCLEUS AND THE CYTOPLASM [J].
FLACH, J ;
BOSSIE, M ;
VOGEL, J ;
CORBETT, A ;
JINKS, T ;
WILLINS, DA ;
SILVER, PA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :8399-8407
[6]   Quality control of mRNA 3′-end processing is linked to the nuclear exosome [J].
Hilleren, P ;
McCarthy, T ;
Rosbash, M ;
Parker, R ;
Jensen, TH .
NATURE, 2001, 413 (6855) :538-542
[7]   The DECD box putative ATPase Sub2p is an early mRNA export factor [J].
Jensen, TH ;
Boulay, J ;
Rosbash, M ;
Libri, D .
CURRENT BIOLOGY, 2001, 11 (21) :1711-1715
[8]   A block to mRNA nuclear export in S. cerevisiae leads to hyperadenylation of transcripts that accumulate at the site of transcription [J].
Jensen, TH ;
Patricio, K ;
McCarthy, T ;
Rosbash, M .
MOLECULAR CELL, 2001, 7 (04) :887-898
[9]   Uncoupling of the hnRNP Npl3p from mRNAs during the stress-induced block in mRNA export [J].
Krebber, H ;
Taura, T ;
Lee, MS ;
Silver, PA .
GENES & DEVELOPMENT, 1999, 13 (15) :1994-2004
[10]   A protein that shuttles between the nucleus and the cytoplasm is an important mediator of RNA export [J].
Lee, MS ;
Henry, M ;
Silver, PA .
GENES & DEVELOPMENT, 1996, 10 (10) :1233-1246