The presence of multiple introns is essential for ERECTA expression in Arabidopsis

被引:44
作者
Karve, Rucha [1 ]
Liu, Wusheng [1 ]
Willet, Spencer G. [1 ]
Torii, Keiko U. [2 ]
Shpak, Elena D. [1 ]
机构
[1] Univ Tennessee, Dept Biochem Cellular & Mol Biol, Knoxville, TN 37996 USA
[2] Univ Washington, Dept Biol, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
gene expression; intron-mediated enhancement; splicing; intron; ERECTA; EXON-JUNCTION COMPLEX; INCREASE GENE-EXPRESSION; MESSENGER-RNA; MEDIATED ENHANCEMENT; TRANSCRIPTIONAL ELONGATION; POLY(A)-BINDING PROTEIN; TRANSLATION INITIATION; RECEPTOR KINASES; SPLICING FACTORS; NUCLEAR EXPORT;
D O I
10.1261/rna.2825811
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
Gene expression in eukaryotes is often enhanced by the presence of introns. Depending on the specific gene, this enhancement can be minor or very large and occurs at both the transcriptional and post-transcriptional levels. The Arabidopsis ERECTA gene contains 27 exons encoding a receptor-like kinase that promotes cell proliferation and inhibits cell differentiation in above-ground plant organs. The expression of ERECTA very strongly depends on the presence of introns. The intronless ERECTA gene does not rescue the phenotype of erecta mutant plants and produces about 500-900 times less protein compared with the identical construct containing introns. This result is somewhat surprising as the region upstream of the ERECTA coding sequence effectively promotes the expression of extraneous genes. Here, we demonstrate that introns are essential for ERECTA mRNA accumulation and, to a lesser extent, for mRNA utilization in translation. Since mRNA produced by intronless ERECTA is degraded at the 39 end, we speculate that introns increase mRNA accumulation through increasing its stability at least in part. No individual intron is absolutely necessary for ERECTA expression, but rather multiple introns in specific locations increase ERECTA expression in an additive manner. The ability of introns to promote ERECTA expression might be linked to the process of splicing and not to a particular intron sequence.
引用
收藏
页码:1907 / 1921
页数:15
相关论文
共 70 条
[1]   Widespread use of poly(A) tail length control to accentuate expression of the yeast transcriptome [J].
Beilharz, Traude H. ;
Preiss, Thomas .
RNA, 2007, 13 (07) :982-997
[2]   Biochemical characterisation of cap-poly(A) synergy in rabbit reticulocyte lysates:: the eIF4G-PABP interaction increases the functional affinity of eIF4E for the capped mRNA 5′-end [J].
Borman, AM ;
Michel, YM ;
Kean, KM .
NUCLEIC ACIDS RESEARCH, 2000, 28 (21) :4068-4075
[3]   Introns and their positions affect the translational activity of mRNA in plant cells [J].
Bourdon, V ;
Harvey, A ;
Lonsdale, DM .
EMBO REPORTS, 2001, 2 (05) :394-398
[4]   COMPARISON OF INTRON-DEPENDENT AND INTRON-INDEPENDENT GENE-EXPRESSION [J].
BUCHMAN, AR ;
BERG, P .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (10) :4395-4405
[5]   INTRONS INCREASE GENE-EXPRESSION IN CULTURED MAIZE CELLS [J].
CALLIS, J ;
FROMM, M ;
WALBOT, V .
GENES & DEVELOPMENT, 1987, 1 (10) :1183-1200
[6]   MAIZE SHRUNKEN-1 INTRON AND EXON REGIONS INCREASE GENE-EXPRESSION IN MAIZE PROTOPLASTS [J].
CLANCY, M ;
VASIL, V ;
HANNAH, LC ;
VASIL, IK .
PLANT SCIENCE, 1994, 98 (02) :151-161
[7]   Floral dip:: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana [J].
Clough, SJ ;
Bent, AF .
PLANT JOURNAL, 1998, 16 (06) :735-743
[8]   The leader intron of Arabidopsis thaliana genes encoding cytochrome c oxidase subunit 5c promotes high-level expression by increasing transcript abundance and translation efficiency [J].
Curi, GC ;
Chan, RL ;
Gonzalez, DH .
JOURNAL OF EXPERIMENTAL BOTANY, 2005, 56 (419) :2563-2571
[9]  
DEAN C, 1989, PLANT CELL, V1, P201, DOI 10.1105/tpc.1.2.201
[10]   THYMIDYLATE SYNTHASE GENE-EXPRESSION IS STIMULATED BY SOME (BUT NOT ALL) INTRONS [J].
DENG, TL ;
LI, Y ;
JOHNSON, LF .
NUCLEIC ACIDS RESEARCH, 1989, 17 (02) :645-658