Splicing of constitutive upstream introns is essential for the recognition of intra-exonic suboptimal splice sites in the thrombopoietin gene

被引:26
作者
Romano, M
Marcucci, R
Baralle, FE
机构
[1] Int Ctr Genet Engn & Biotechnol, I-34012 Trieste, Italy
[2] Univ Trieste, Dept Physiol & Pathol, I-34127 Trieste, Italy
关键词
D O I
10.1093/nar/29.4.886
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 human thrombopoietin (TPO) gene, which codes for the principal cytokine involved in platelet maturation, shows a peculiar alternative splicing of its last exon, where an intra-exonic 116 nt alternative intron is spliced out in: a fraction of its mRNA, To characterize the molecular mechanism underlying this alternative splicing, minigenes of TPO genomic constructs with variable exon-intron configurations or carrying exclusively the TPO cDNA were generated and transiently transfected in the Hep3B cell line. We have found that the final rate of the alternative intron splicing is determined by three elements: the presence of upstream constitutive introns, the suboptimal splice sites of the alternative intron and the length of the alternative intron itself, Our results indicate that the-recognition of suboptimal intra-exonic splice junctions in the TPO gene is influenced by the assembly of the spliceosome complex on constitutive introns and by a qualitative scanning of the sequence by-the transcriptional/splicing machinery complex primed by upstream splicing signals.
引用
收藏
页码:886 / 894
页数:9
相关论文
共 39 条
[1]   SPLICING OF BALBIANI RING-1 GENE PREMESSENGER RNA OCCURS SIMULTANEOUSLY WITH TRANSCRIPTION [J].
BAUREN, G ;
WIESLANDER, L .
CELL, 1994, 76 (01) :183-192
[2]   SPLICE SITE SELECTION, RATE OF SPLICING, AND ALTERNATIVE SPLICING ON NASCENT TRANSCRIPTS [J].
BEYER, AL ;
OSHEIM, YN .
GENES & DEVELOPMENT, 1988, 2 (06) :754-765
[4]   CLONING AND CHARACTERIZATION OF THE HUMAN MEGAKARYOCYTE GROWTH AND DEVELOPMENT FACTOR (MGDF) GENE [J].
CHANG, MS ;
MCNINCH, J ;
BASU, R ;
SHUTTER, J ;
HSU, RY ;
PERKINS, C ;
MAR, V ;
SUGGS, S ;
WELCHER, A ;
LI, L ;
LU, H ;
BARTLEY, T ;
HUNT, P ;
MARTIN, F ;
SAMAL, B ;
BOGENBERGER, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (02) :511-514
[5]   LARGE EXON SIZE DOES NOT LIMIT SPLICING IN-VIVO [J].
CHEN, IT ;
CHASIN, LA .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :2140-2146
[6]   Functional association between promoter structure and transcript alternative splicing [J].
Cramer, P ;
Pesce, CG ;
Baralle, FE ;
Kornblihtt, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11456-11460
[7]   MULTIPLE SPLICING SIGNALS CONTROL ALTERNATIVE INTRON RETENTION OF BOVINE GROWTH-HORMONE PRE-MESSENGER-RNA [J].
DIRKSEN, WP ;
SUN, QA ;
ROTTMAN, FM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (10) :5346-5352
[8]   SELECTION OF SPLICE SITES IN PRE-MESSENGER-RNAS WITH SHORT INTERNAL EXONS [J].
DOMINSKI, Z ;
KOLE, R .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :6075-6083
[9]   RNA SECONDARY STRUCTURE REPRESSION OF A MUSCLE-SPECIFIC EXON IN HELA-CELL NUCLEAR EXTRACTS [J].
DORVAL, BC ;
CARAFA, YD ;
SIRANDPUGNET, P ;
GALLEGO, M ;
BRODY, E ;
MARIE, J .
SCIENCE, 1991, 252 (5014) :1823-1828
[10]   A short sequence within two purine-rich enhancers determines 5′ splice site specificity [J].
Elrick, LL ;
Humphrey, MB ;
Cooper, TA ;
Berget, SM .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (01) :343-352