Substrate selectivity of Exportin 5 and Dicer in the biogenesis of microRNAs

被引:124
作者
Lund, E. [1 ]
Dahlberg, J. E. [1 ]
机构
[1] Univ Wisconsin, Madison, WI 53706 USA
关键词
D O I
10.1101/sqb.2006.71.050
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
Each step in the biogenesis of microRNAs (miRNAs) depends on recognition of a correct substrate and efficient transport or processing of that RNA. Exportin5 (Exp5) and Dicer are proteins that mediate two key steps in this cascade, the nuclear export and cytoplasmic processing of microRNA precursor (pre-miRNAs). Xenopus laevis oocytes, eggs, and embryos constitute convenient experimental systems in which to study the substrate specificity of these proteins because specific RNAs or proteins can be injected directly into different subcellular compartments. We have used the Xenopus system and in vitro processing to define and compare the specificities of Exp5 and Dicer. Although both proteins act on many of the same substrates, we show flat they recognize different structure elements of these RNAs. Our studies also revealed several unexpected activities. For example, Exp5 can mediate export of unspliced pre-mRNAs and excised lariat introns if these RNAs contain an aptamer sequence that itself is an Exp5 export substrate. Finally, we demonstrate that maturation of Xenopus oocytes into eggs leads to a large increase in Dicer activity, suggesting that miRNA biogenesis is subject to developmental control.
引用
收藏
页码:59 / 66
页数:8
相关论文
共 40 条
[21]   Adenovirus VA1 noncoding RNA can inhibit small interfering RNA and microRNA biogenesis [J].
Lu, SH ;
Cullen, BR .
JOURNAL OF VIROLOGY, 2004, 78 (23) :12868-12876
[22]   Nuclear export of microRNA precursors [J].
Lund, E ;
Güttinger, S ;
Calado, A ;
Dahlberg, JE ;
Kutay, U .
SCIENCE, 2004, 303 (5654) :95-98
[23]   Structural basis for double-stranded RNA processing by dicer [J].
MacRae, IJ ;
Zhou, KH ;
Li, F ;
Repic, A ;
Brooks, AN ;
Cande, WZ ;
Adams, PD ;
Doudna, JA .
SCIENCE, 2006, 311 (5758) :195-198
[24]   A human, ATP-independent, RISC assembly machine fueled by pre-miRNA [J].
Maniataki, E ;
Mourelatos, Z .
GENES & DEVELOPMENT, 2005, 19 (24) :2979-2990
[25]   Translational control by CPEB: A means to the end [J].
Mendez, R ;
Richter, JD .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2001, 2 (07) :521-529
[26]   MiRNAs on the move: miRNA biogenesis and the RNAi machinery [J].
Murchison, EP ;
Hannon, GJ .
CURRENT OPINION IN CELL BIOLOGY, 2004, 16 (03) :223-229
[27]   A MAJOR DEVELOPMENTAL TRANSITION IN EARLY XENOPUS-EMBRYOS .1. CHARACTERIZATION AND TIMING OF CELLULAR-CHANGES AT THE MIDBLASTULA STAGE [J].
NEWPORT, J ;
KIRSCHNER, M .
CELL, 1982, 30 (03) :675-686
[28]   In situ fluorescence analysis demonstrates active siRNA exclusion from the nucleus by Exportin 5 [J].
Ohrt, T ;
Merkle, D ;
Birkenfeld, K ;
Echeverri, CJ ;
Schwille, P .
NUCLEIC ACIDS RESEARCH, 2006, 34 (05) :1369-1380
[29]   The constitutive transport element (CTE) of Mason-Pfizer monkey virus (MPMV) accesses a cellular mRNA export pathway [J].
Pasquinelli, AE ;
Ernst, RK ;
Lund, E ;
Grimm, C ;
Zapp, ML ;
Rekosh, D ;
Hammarskjöld, ML ;
Dahlberg, JE .
EMBO JOURNAL, 1997, 16 (24) :7500-7510
[30]   The matrix protein of vesicular stomatitis virus inhibits nucleocytoplasmic transport when it is in the nucleus and associated with nuclear pore complexes [J].
Petersen, JM ;
Her, LS ;
Varvel, V ;
Lund, E ;
Dahlberg, JE .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (22) :8590-8601