Effect of 5′UTR introns on gene expression in Arabidopsis thaliana

被引:180
作者
Chung, Betty Y. W.
Simons, Cas
Firth, Andrew E.
Brown, Chris M.
Hellens, Roger P. [1 ]
机构
[1] HortRes, Auckland, New Zealand
[2] Univ Otago, Dept Biochem, Dunedin, New Zealand
[3] Inst Mol Biosci, Brisbane, Qld, Australia
[4] Univ Coll Cork, Biosci Inst, Cork, Ireland
关键词
D O I
10.1186/1471-2164-7-120
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The majority of introns in gene transcripts are found within the coding sequences (CDSs). A small but significant fraction of introns are also found to reside within the untranslated regions (5 ' UTRs and 3 ' UTRs) of expressed sequences. Alignment of the whole genome and expressed sequence tags (ESTs) of the model plant Arabidopsis thaliana has identified introns residing in both coding and non-coding regions of the genome. Results: A bioinformatic analysis revealed some interesting observations: (1) the density of introns in 5 ' UTRs is similar to that in CDSs but much higher than that in 3 ' UTRs; (2) the 5 ' UTR introns are preferentially located close to the initiating ATG codon; (3) introns in the 5 ' UTRs are, on average, longer than introns in the CDSs and 3 ' UTRs; and (4) 5 ' UTR introns have a different nucleotide composition to that of CDS and 3 ' UTR introns. Furthermore, we show that the 5 ' UTR intron of the A. thaliana EF1 alpha-A3 gene affects the gene expression and the size of the 5 ' UTR intron influences the level of gene expression. Conclusion: Introns within the 5 ' UTR show specific features that distinguish them from introns that reside within the coding sequence and the 3 ' UTR. In the EF1 alpha-A3 gene, the presence of a long intron in the 5 ' UTR is sufficient to enhance gene expression in plants in a size dependent manner.
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页数:13
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共 52 条
[1]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[2]   Plant gene expression in the age of systems biology: integrating transcriptional and post-transcriptional events [J].
Belostotsky, DA ;
Rose, AB .
TRENDS IN PLANT SCIENCE, 2005, 10 (07) :347-353
[3]   GenBank: update [J].
Benson, DA ;
Karsch-Mizrachi, I ;
Lipman, DJ ;
Ostell, J ;
Wheeler, DL .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D23-D26
[4]   Splicing signals and factors in plant intron removal [J].
Brown, JWS ;
Simpson, CG ;
Thow, G ;
Clark, GP ;
Jennings, SN ;
Medina-Escobar, N ;
Haupt, S ;
Chapman, SC ;
Oparka, KJ .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2002, 30 :146-149
[5]  
BRUCE WB, 1990, PLANT CELL, V2, P1081, DOI 10.1105/tpc.2.11.1081
[6]   PREDICTION OF HUMAN MESSENGER-RNA DONOR AND ACCEPTOR SITES FROM THE DNA-SEQUENCE [J].
BRUNAK, S ;
ENGELBRECHT, J ;
KNUDSEN, S .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 220 (01) :49-65
[7]   INTRONS INCREASE GENE-EXPRESSION IN CULTURED MAIZE CELLS [J].
CALLIS, J ;
FROMM, M ;
WALBOT, V .
GENES & DEVELOPMENT, 1987, 1 (10) :1183-1200
[8]   Tissue-dependent enhancement of transgene expression by introns of replacement histone H3 genes of Arabidopsis [J].
Chaubet-Gigot, N ;
Kapros, T ;
Flenet, M ;
Kahn, K ;
Gigot, C ;
Waterborg, JH .
PLANT MOLECULAR BIOLOGY, 2001, 45 (01) :17-30
[9]   Floral dip:: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana [J].
Clough, SJ ;
Bent, AF .
PLANT JOURNAL, 1998, 16 (06) :735-743
[10]   WebLogo: A sequence logo generator [J].
Crooks, GE ;
Hon, G ;
Chandonia, JM ;
Brenner, SE .
GENOME RESEARCH, 2004, 14 (06) :1188-1190