Perinuclear Mlp proteins downregulate gene expression in response to a defect in mRNA export

被引:112
作者
Vinciguerra, P [1 ]
Iglesias, N [1 ]
Camblong, J [1 ]
Zenklusen, D [1 ]
Stutz, F [1 ]
机构
[1] Univ Geneva, Dept Cell Biol, CH-1211 Geneva 4, Switzerland
关键词
Mlp proteins; mRNP biogenesis and export; Nab2p; transcription; Yra1p;
D O I
10.1038/sj.emboj.7600527
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 mRNA export adaptor Yra1p/ REF contributes to nascent mRNP assembly and recruitment of the export receptor Mex67p. yra1 mutants exhibit mRNA export defects and a decrease in LacZ reporter and certain endogenous transcripts. The loss of Mlp1p/ Mlp2p, two TPR- like proteins attached to nuclear pores, rescues LacZ mRNA levels and increases their appearance in the cytoplasm, without restoring bulk poly( A) + RNA export. Chromatin immunoprecipitation, FISH and pulse- chase experiments indicate that Mlps downregulate LacZ mRNA synthesis in a yra1 mutant strain. Microarray analyses reveal that Mlp2p also reduces a subset of cellular transcripts in the yra1 mutant. Finally, we show that Yra1p genetically interacts with the shuttling mRNA- binding protein Nab2p and that loss of Mlps rescues the growth defect of yra1 and nab2 but not other mRNA export mutants. We propose that Nab2p and Yra1p are required for proper mRNP docking to the Mlp platform. Defects in Yra1p prevent mRNPs from crossing the Mlp gate and this block negatively feeds back on the transcription of a subset of genes, suggesting that Mlps link mRNA transcription and export.
引用
收藏
页码:813 / 823
页数:11
相关论文
共 37 条
[1]   Functional analysis of Tpr: Identification of nuclear pore complex association and nuclear localization domains and a role in mRNA export [J].
Bangs, P ;
Burke, B ;
Powers, C ;
Craig, R ;
Purohit, A ;
Doxsey, S .
JOURNAL OF CELL BIOLOGY, 1998, 143 (07) :1801-1812
[2]   Identification of a regulated pathway for nuclear pre-mRNA turnover [J].
Bousquet-Antonelli, C ;
Presutti, C ;
Tollervey, D .
CELL, 2000, 102 (06) :765-775
[3]   A nuclear 3′-5′ exonuclease involved in mRNA degradation interacts with poly(A) polymerase and the hnRNA protein Npl3p [J].
Burkard, KTD ;
Butler, JS .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (02) :604-616
[4]   Genome-wide localization of the nuclear transport machinery couples transcriptional status and nuclear organization [J].
Casolari, JM ;
Brown, CR ;
Komili, S ;
West, J ;
Hieronymus, H ;
Silver, PA .
CELL, 2004, 117 (04) :427-439
[5]   A protein complex containing Tho2, Hpr1, Mft1 and a novel protein, Thp2, connects transcription elongation with mitotic recombination in Saccharomyces cerevisiae [J].
Chávez, S ;
Beilharz, T ;
Rondón, AG ;
Erdjument-Bromage, H ;
Tempst, P ;
Svejstrup, JQ ;
Lithgow, T ;
Aguilera, A .
EMBO JOURNAL, 2000, 19 (21) :5824-5834
[6]   Identification of protein p270/Tpr as a constitutive component of the nuclear pore complex-attached intranuclear filaments [J].
Cordes, VC ;
Reidenbach, S ;
Rackwitz, HR ;
Franke, WW .
JOURNAL OF CELL BIOLOGY, 1997, 136 (03) :515-529
[7]   Molecular segments of protein Tpr that confer nuclear targeting and association with the nuclear pore complex [J].
Cordes, VC ;
Hase, ME ;
Müller, L .
EXPERIMENTAL CELL RESEARCH, 1998, 245 (01) :43-56
[8]   Nuclear architecture and spatial positioning help establish transcriptional states of telomeres in yeast [J].
Feuerbach, F ;
Galy, V ;
Trelles-Sticken, E ;
Fromont-Racine, M ;
Jacquier, A ;
Gilson, E ;
Olivo-Marin, JC ;
Scherthan, H ;
Nehrbass, U .
NATURE CELL BIOLOGY, 2002, 4 (03) :214-221
[9]   Nuclear retention of unspliced mRNAs in yeast is mediated by perinuclear Mlp1 [J].
Galy, V ;
Gadal, O ;
Fromont-Racine, M ;
Romano, A ;
Jacquier, A ;
Nehrbass, U .
CELL, 2004, 116 (01) :63-73
[10]   Nuclear pore complexes in the organization of silent telomeric chromatin [J].
Galy, V ;
Olivo-Marin, JC ;
Scherthan, H ;
Doye, V ;
Rascalou, N ;
Nehrbass, U .
NATURE, 2000, 403 (6765) :108-112