Multifunctional regulatory proteins that control gene expression in both the nucleus and the cytoplasm

被引:87
作者
Wilkinson, MF
Shyu, AB
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Univ Texas, Sch Med, Dept Biochem & Mol Biol, Houston, TX 77030 USA
关键词
D O I
10.1002/bies.1113
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 multistep pathway of eukaryotic gene expression involves a series of highly regulated events in the nucleus and cytoplasm. In the nucleus, genes are transcribed into pre-messenger RNAs which undergo a series of nuclear processing steps. Mature mRNAs are then transported to the cytoplasm, where they are translated into protein and degraded at a rate dictated by transcript- and cell-type-specific cues. Until recently, these individual nuclear and cytoplasmic events were thought to be primarily regulated by different RNA- and DNA-binding proteins that are localized either only in the nucleus or only the cytoplasm. Here, we describe multifunctional proteins that control both nuclear and cytoplasmic steps of gene expression. One such class of multifunctional proteins (e.g., Bicoid and Y-box proteins) regulates both transcription and translation whereas another class (e.g., Sex-lethal) regulates both nuclear RNA processing and translation. Other events controlled by multifunctional proteins include assembly of spliceosome components, spliceosome recycling, RNA editing, cytoplasmic mRNA localization, and cytoplasmic RNA stability. The existence of multifunctional proteins may explain the paradoxical involvement of the nucleus in an RNA surveillance pathway (nonsense-mediated decay) that detects cytoplasmic signals (premature termination codons). We speculate that shuttling multifunctional proteins serve to efficiently link RNA metabolism in the cytoplasmic and nuclear compartments. (C) 2001 John Wiley & Sons, Inc.
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收藏
页码:775 / 787
页数:13
相关论文
共 86 条
[1]   An AU-rich sequence element (UUUN[A/U]U) downstream of the edited C in apolipoprotein B mRNA is a high-affinity binding site for Apobec-1:: Binding of Apobec-1 to this motif in the 3′ untranslated region of c-myc increases mRNA stability [J].
Anant, S ;
Davidson, NO .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (06) :1982-1992
[2]   A NOVEL GENE, TRANSLIN, ENCODES A RECOMBINATION HOTSPOT BINDING-PROTEIN ASSOCIATED WITH CHROMOSOMAL TRANSLOCATIONS [J].
AOKI, K ;
SUZUKI, K ;
SUGANO, T ;
TASAKA, T ;
NAKAHARA, K ;
KUGE, O ;
OMORI, A ;
KASAI, M .
NATURE GENETICS, 1995, 10 (02) :167-174
[3]   The role of exportin-t in selective nuclear export of mature tRNAs [J].
Arts, GJ ;
Kuersten, S ;
Romby, P ;
Ehresmann, B ;
Mattaj, IW .
EMBO JOURNAL, 1998, 17 (24) :7430-7441
[4]   Embryo deadenylation element-dependent deadenylation is enhanced by a cis element containing AUU repeats [J].
Audic, Y ;
Omilli, F ;
Osborne, HB .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (12) :6879-6884
[5]   The regulation of the Drosophila msl-2 gene reveals a function for Sex-lethal in translational control [J].
Bashaw, GJ ;
Baker, BS .
CELL, 1997, 89 (05) :789-798
[6]   MAMMALIAN NONSENSE CODONS CAN BE CIS EFFECTORS OF NUCLEAR MESSENGER-RNA HALF-LIFE [J].
BELGRADER, P ;
CHENG, J ;
ZHOU, XB ;
STEPHENSON, LS ;
MAQUAT, LE .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :8219-8228
[7]  
Biamonti G, 1998, CLIN EXP RHEUMATOL, V16, P317
[8]   Protein ligands to HuR modulate its interaction with target mRNAs in vivo [J].
Brennan, CM ;
Gallouzi, IE ;
Steitz, JA .
JOURNAL OF CELL BIOLOGY, 2000, 151 (01) :1-13
[9]   A specific subset of SR proteins shuttles continuously between the nucleus and the cytoplasm [J].
Cáceres, JF ;
Screaton, GR ;
Krainer, AR .
GENES & DEVELOPMENT, 1998, 12 (01) :55-66
[10]   A splicing-dependent regulatory mechanism that detects translation signals [J].
Carter, MS ;
Li, SL ;
Wilkinson, MF .
EMBO JOURNAL, 1996, 15 (21) :5965-5975