The quaking family of RNA-binding proteins Coordinators of the cell cycle and differentiation

被引:35
作者
Biedermann, Bjoern [1 ]
Hotz, Hans-Rudolf [1 ]
Ciosk, Rafal [1 ]
机构
[1] Friedrich Miescher Inst Biomed Res, Basel, Switzerland
关键词
quaking; GLD-1; HOW; STAR protein; RNA regulation; development; differentiation; cell cycle; cell fate specification; TUMOR-SUPPRESSOR GENE; MESSENGER-RNA; POSTTRANSCRIPTIONAL REGULATION; TRANSLATIONAL REPRESSION; CAENORHABDITIS-ELEGANS; SIGNAL-TRANSDUCTION; STAR PROTEIN; STEM-CELLS; ISOFORMS; GLD-1;
D O I
10.4161/cc.9.10.11533
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transcriptional and epigenetic control of gene expression is critical for cell fate specification, commitment and terminal differentiation during development. However, also regulatory RNAs and RNA-binding proteins have emerged as critical developmental regulators. They control various aspects of mRNA metabolism such as stability, translation and localization, and similar to some transcriptional regulators, such as PAX5 and MYC, can affect gene expression on a massive scale. Consistently, defects in many mRNA regulators have been implicated in a number of human disorders, including cancer. Quaking-related (QR) proteins are conserved RNA-binding proteins of the STAR (signal transduction and activation of RNA) family. QR proteins regulate expression of diverse mRNA targets by various mechanisms, play essential roles in a whole host of developmental decisions, and function as tumor suppressors. This review discusses several best-studied members of the QR family, their developmental functions, molecular mechanisms, representative mRNA targets, and their intriguing ability to coordinately control the cell cycle and a wide range of differentiation pathways.
引用
收藏
页码:1929 / 1933
页数:5
相关论文
共 67 条
[1]  
Baehrecke EH, 1997, DEVELOPMENT, V124, P1323
[2]   Translational Repression of Cyclin E Prevents Precocious Mitosis and Embryonic Gene Activation during C. elegans Meiosis [J].
Biedermann, Bjoern ;
Wright, Jane ;
Senften, Mathias ;
Kalchhauser, Irene ;
Sarathy, Gautham ;
Lee, Min-Ho ;
Ciosk, Rafal .
DEVELOPMENTAL CELL, 2009, 17 (03) :355-364
[3]   let-7 microRNAs in development, stem cells and cancer [J].
Buessing, Ingo ;
Slack, Frank J. ;
Grosshans, Helge .
TRENDS IN MOLECULAR MEDICINE, 2008, 14 (09) :400-409
[4]   MicroRNA functions [J].
Bushati, Natascha ;
Cohen, Stephen M. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2007, 23 :175-205
[5]   Structure-function analysis of Qk1:: a lethal point mutation in mouse quaking prevents homodimerization [J].
Chen, TP ;
Richard, S .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (08) :4863-4871
[6]   The selective RNA-binding protein quaking I (QKI) is necessary and sufficient for promoting oligodendroglia differentiation [J].
Chen, Yuntao ;
Tian, Donghua ;
Ku, Li ;
Osterhout, Donna J. ;
Feng, Yue .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (32) :23553-23560
[7]   Contrasting effects of ENU induced embryonic lethal mutations of the quaking gene [J].
Cox, RD ;
Hugill, A ;
Shedlovsky, A ;
Noveroske, JK ;
Best, S ;
Justice, MJ ;
Lehrach, H ;
Dove, WF .
GENOMICS, 1999, 57 (03) :333-341
[8]   A conserved RNA-binding protein controls germline stem cells in Caenorhabditis elegans [J].
Crittenden, SL ;
Bernstein, DS ;
Bachorik, JL ;
Thompson, BE ;
Gallegos, M ;
Petcherski, AG ;
Moulder, G ;
Barstead, R ;
Wickens, M ;
Kimble, J .
NATURE, 2002, 417 (6889) :660-663
[9]   Two zinc finger proteins, OMA-1 and OMA-2, are redundantly required for oocyte maturation in C-elegans [J].
Detwiler, MR ;
Reuben, M ;
Li, XM ;
Rogers, R ;
Lin, RL .
DEVELOPMENTAL CELL, 2001, 1 (02) :187-199
[10]   Characterization of Sam68-like mammalian proteins SLM-1 and SLM-2: SLM-1 is a Src substrate during mitosis [J].
Di Fruscio, M ;
Chen, TP ;
Richard, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :2710-2715