Futile cycle of transcription initiation and termination modulates the response to nucleotide shortage in S-cerevisiae

被引:80
作者
Thiebaut, Marilyne [2 ]
Colin, Jessie [2 ]
Neil, Helen [3 ]
Jacquier, Alain [3 ]
Seraphin, Bertrand [1 ,4 ]
Lacroute, Francois [1 ,4 ]
Libri, Domenico [2 ]
机构
[1] CNRS, Ctr Genet Mol, UPR2167, Equipe Labellisee La Ligue, F-91190 Gif Sur Yvette, France
[2] Aarhus Univ, Ctr mRNP Biogenesis & Metab, DK-8000 Aarhus C, Denmark
[3] Inst Pasteur, Unite Genet Interact Macromol, CNRS, URA2171, F-75015 Paris, France
[4] Univ Paris 06, F-75005 Paris, France
基金
新加坡国家研究基金会;
关键词
D O I
10.1016/j.molcel.2008.08.010
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
Hidden transcription in eukaryotes carries a large potential of regulatory functions that are only recently beginning to emerge. Cryptic unstable transcripts (CUTs) are generated by RNA polymerase II (Pol II) and rapidly degraded after transcription in wildtype yeast cells. Whether CUTs or the act of transcription without RNA production have a function is presently unclear. We describe here a nonconventional mechanism of transcriptional regulation that relies on the selection of alternative transcription start sites to generate CUTs or mRNAs. Transcription from TATA box proximal start sites generates unstable transcripts and downregulates expression of the URA2 gene under repressing conditions. Uracil deprivation activates selection of distal start sites, leading to the production of stable mRNAs. We describe the elements that govern degradation of the CUT and activation of mRNA production by downstream transcription initiation. Importantly, we show that a similar mechanism applies to other genes in the nucleotides biogenesis pathway.
引用
收藏
页码:671 / 682
页数:12
相关论文
共 41 条
[31]   THE YEAST SUA7 GENE ENCODES A HOMOLOG OF HUMAN TRANSCRIPTION FACTOR TFIIB AND IS REQUIRED FOR NORMAL START SITE SELECTION INVIVO [J].
PINTO, I ;
WARE, DE ;
HAMPSEY, M .
CELL, 1992, 68 (05) :977-988
[32]  
PINTO I, 1994, J BIOL CHEM, V269, P30569
[33]   CORRELATION BETWEEN RESTRICTION MAP, GENETIC-MAP AND CATALYTIC FUNCTIONS IN THE GENE-COMPLEX URA2 [J].
POTIER, S ;
SOUCIET, JL ;
LACROUTE, F .
MOLECULAR & GENERAL GENETICS, 1987, 209 (02) :283-289
[34]   Genome-wide distribution of yeast RNA polymerase II and its control by Sen1 helicase [J].
Steinmetz, Eric J. ;
Warren, Christopher L. ;
Kuehner, Jason N. ;
Panbehi, Bahman ;
Ansari, Aseem Z. ;
Brow, David A. .
MOLECULAR CELL, 2006, 24 (05) :735-746
[35]   Transcription termination and nuclear degradation of cryptic unstable transcripts: A role for the Nrd1-Nab3 pathway in genome surveillance [J].
Thiebaut, Marilyne ;
Kisseleva-Romanova, Elena ;
Rougemaille, Mathieu ;
Boulay, Jocelyne ;
Libri, Domenico .
MOLECULAR CELL, 2006, 23 (06) :853-864
[36]   A new yeast poly(A) polymerase complex involved in RNA quality control [J].
Vanácová, S ;
Wolf, J ;
Martin, G ;
Blank, D ;
Dettwiler, S ;
Friedlein, A ;
Langen, H ;
Keith, G ;
Keller, W .
PLOS BIOLOGY, 2005, 3 (06) :986-997
[37]   Nrd1 interacts with the nuclear exosome for 3′ processing of RNA polymerase II transcripts [J].
Vasiljeva, L ;
Buratowski, S .
MOLECULAR CELL, 2006, 21 (02) :239-248
[38]   The Nrd1-Nab3-Sen1 termination complex interacts with the Ser5-phosphorylated RNA polymerase II C-terminal domain [J].
Vasiljeva, Lidia ;
Kim, Minkyu ;
Mutschler, Hannes ;
Buratowski, Stephen ;
Meinhart, Anton .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2008, 15 (08) :795-804
[39]  
VILLA T, 2008, BIOCH BIOPH IN PRESS
[40]   Cryptic Pol II transcripts are degraded by a nuclear quality control pathway involving a new poly(A) polymerase [J].
Wyers, F ;
Rougemaille, M ;
Badis, G ;
Rousselle, JC ;
Dufour, ME ;
Boulay, J ;
Régnault, B ;
Devaux, F ;
Namane, A ;
Séraphin, B ;
Libri, D ;
Jacquier, A .
CELL, 2005, 121 (05) :725-737