Growth-regulated expression and G0-specific turnover of the mRNA that encodes URH49, a mammalian DExH/D box protein that is highly related to the mRNA export protein UAP56

被引:61
作者
Pryor, A
Tung, L
Yang, Z
Kapadia, F
Chang, TH
Johnson, LF [1 ]
机构
[1] Ohio State Univ, Ohio State Biochem Program, Columbus, OH 43210 USA
[2] Ohio State Univ, Mol Cellular & Dev Biol Program, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Mol Genet, Columbus, OH 43210 USA
关键词
D O I
10.1093/nar/gkh347
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
URH49 is a mammalian protein that is 90% identical to the DExH/D box protein UAP56, an RNA helicase that is important for splicing and nuclear export of mRNA. Although Saccharomyces cerevisiae and Drosophila express only a single protein corresponding to UAP56, mRNAs encoding URH49 and UAP56 are both expressed in human and mouse cells. Both proteins interact with the mRNA export factor Aly and both are able to rescue the loss of Sub2p (the yeast homolog of UAP56), indicating that both proteins have similar functions. UAP56 mRNA is more abundant than URH49 mRNA in many tissues, although in testes URH49 mRNA is much more abundant. UAP56 and URH49 mRNAs are present at similar levels in proliferating cultured cells. However, when the cells enter quiescence, the URH49 mRNA level decreases 3-6-fold while the UAP56 mRNA level remains relatively constant. The amount of URH49 mRNA increases to the level found in proliferating cells within 5 h when quiescent cells are growth-stimulated or when protein synthesis is inhibited. URH49 mRNA is relatively unstable (T-1/2 = 4 h) in quiescent cells, but is stabilized immediately following growth stimulation or inhibition of protein synthesis. In contrast, there is much less change in the content or stability of UAP56 mRNA following growth stimulation. Our observations suggest that in mammalian cells, two UAP56-like RNA helicases are involved in splicing and nuclear export of mRNA. Differential expression of these helicases may lead to quantitative or qualitative changes in mRNA expression.
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页码:1857 / 1865
页数:9
相关论文
共 57 条
[11]  
Herold A, 2001, RNA, V7, P1768
[12]   Pre-mRNA splicing: Awash in a sea of proteins [J].
Jurica, MS ;
Moore, MJ .
MOLECULAR CELL, 2003, 12 (01) :5-14
[13]   HEL/UAP56 binds cotranscriptionally to the Balbiani ring pre-mRNA in an intron-independent manner and accompanies the BR mRNP to the nuclear pore [J].
Kiesler, E ;
Miralles, F ;
Visa, N .
CURRENT BIOLOGY, 2002, 12 (10) :859-862
[14]   Deletion of MUD2, the yeast homolog of U2AF65, can bypass the requirement for Sub2, an essential spliceosomal ATPase [J].
Kistler, AL ;
Guthrie, C .
GENES & DEVELOPMENT, 2001, 15 (01) :42-49
[15]   EXPRESSION OF A SET OF GROWTH-RELATED IMMEDIATE EARLY GENES IN BALB-C 3T3 CELLS - COORDINATE REGULATION WITH C-FOS OR C-MYC [J].
LAU, LF ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (05) :1182-1186
[16]   The spliceosome deposits multiple proteins 20-24 nucleotides upstream of mRNA exon-exon junctions [J].
Le Hir, H ;
Izaurralde, E ;
Maquat, LE ;
Moore, MJ .
EMBO JOURNAL, 2000, 19 (24) :6860-6869
[17]   The protein Mago provides a link between splicing and mRNA localization [J].
Le Hir, H ;
Gatfield, D ;
Braun, IC ;
Forler, D ;
Izaurralde, E .
EMBO REPORTS, 2001, 2 (12) :1119-1124
[18]   The exon-exon junction complex provides a binding platform for factors involved in mRNA export and nonsense-mediated mRNA decay [J].
Le Hir, H ;
Gatfield, D ;
Izaurralde, E ;
Moore, MJ .
EMBO JOURNAL, 2001, 20 (17) :4987-4997
[19]   HIGH-LEVEL EXPRESSION IN MALE GERM-CELLS OF MURINE P68 RNA HELICASE MESSENGER-RNA [J].
LEMAIRE, L ;
HEINLEIN, UAO .
LIFE SCIENCES, 1993, 52 (11) :917-926
[20]   THE PROTEIN ENCODED BY A MURINE MALE GERM CELL-SPECIFIC TRANSCRIPT IS A PUTATIVE ATP-DEPENDENT RNA HELICASE [J].
LEROY, P ;
ALZARI, P ;
SASSOON, D ;
WOLGEMUTH, D ;
FELLOUS, M .
CELL, 1989, 57 (04) :549-559