Splicing is required for rapid and efficient mRNA export in metazoans

被引:301
作者
Luo, MJ [1 ]
Reed, R [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.96.26.14937
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pre-mRNA splicing is among the last known nuclear events before export of mature mRNA to the cytoplasm, At present; it is not known whether splicing and mRNA export are biochemically coupled processes. In this study, we have injected pre-mRNAs containing a single intron or the same mRNAs lacking an intron (Delta i-mRNAs) into Xenopus oocyte nuclei. We find that the spliced mRNAs are exported much more rapidly and efficiently than the identical Delta i-mRNAs. Moreover, competition studies using excess Delta i-mRNA indicate that different factor(s) are involved in the inefficient export df Delta i-mRNA vs. the efficient export of spliced mRNA. Consistent with this conclusion, spliced mRNA and Delta i-mRNA, though identical in sequence, are assembled into different messenger ribonucleoprotein particles (mRNP) in vitro. Strikingly, the mRNA in the spliced mRNP, but not in the Delta i-mRNP, is exported rapidly and efficiently. We conclude that splicing generates a specific nucleoprotein complex that targets mRNA for export. Our results, revealing a link between splicing and efficient mRNA export, may explain the reports that an intron is required for efficient expression of many protein-coding genes in metazoans.
引用
收藏
页码:14937 / 14942
页数:6
相关论文
共 63 条
[41]   THE INTRON REQUIREMENT FOR IMMUNOGLOBULIN GENE-EXPRESSION IS DEPENDENT UPON THE PROMOTER [J].
NEUBERGER, MS ;
WILLIAMS, GT .
NUCLEIC ACIDS RESEARCH, 1988, 16 (14) :6713-6724
[42]   The importin-beta family member Crm1p bridges the interaction between Rev and the nuclear pore complex during nuclear export [J].
Neville, M ;
Stutz, F ;
Lee, L ;
Davis, LI ;
Rosbash, M .
CURRENT BIOLOGY, 1997, 7 (10) :767-775
[43]   Inhibition of mRNA export in vertebrate cells by nuclear export signal conjugates [J].
Pasquinelli, AE ;
Powers, MA ;
Lund, E ;
Forbes, D ;
Dahlberg, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14394-14399
[44]   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
[45]   RAE1 is a shuttling mRNA export factor that binds to a GLEBS-like NUP98 motif at the nuclear pore complex through multiple domains [J].
Pritchard, CEJ ;
Fornerod, M ;
Kasper, LH ;
van Deursen, JMA .
JOURNAL OF CELL BIOLOGY, 1999, 145 (02) :237-253
[46]   Expression of recombinant human ceruloplasmin - An absolute requirement for splicing signals in the expression cassette [J].
Rafiq, M ;
Suen, CKM ;
Choudhury, N ;
Joannou, CL ;
White, KN ;
Evans, RW .
FEBS LETTERS, 1997, 407 (02) :132-136
[48]   Initial splice-site recognition and pairing during pre-mRNA splicing [J].
Reed, R .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (02) :215-220
[49]   INTRON SEQUENCES INVOLVED IN LARIAT FORMATION DURING PRE-MESSENGER RNA SPLICING [J].
REED, R ;
MANIATIS, T .
CELL, 1985, 41 (01) :95-105
[50]   SIMIAN VIRUS-40 LATE TRANSCRIPTS LACKING EXCISABLE INTERVENING SEQUENCES ARE DEFECTIVE IN BOTH STABILITY IN THE NUCLEUS AND TRANSPORT TO THE CYTOPLASM [J].
RYU, WS ;
MERTZ, JE .
JOURNAL OF VIROLOGY, 1989, 63 (10) :4386-4394