Gametophytic selection in Arabidopsis thaliana supports the selective model of intron length reduction

被引:56
作者
Seoighe, C [1 ]
Gehring, C
Hurst, LD
机构
[1] Univ Cape Town, Inst Infect Dis & Mol Med, ZA-7700 Rondebosch, South Africa
[2] Univ Western Cape, Dept Biotechnol, ZA-7535 Bellville, South Africa
[3] Univ Bath, Dept Biol & Biochem, Bath BA2 7AY, Somerset, England
来源
PLOS GENETICS | 2005年 / 1卷 / 02期
关键词
D O I
10.1371/journal.pgen.0010013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Why do highly expressed genes have small introns? This is an important issue, not least because it provides a testing ground to compare selectionist and neutralist models of genome evolution. Some argue that small introns are selectively favoured to reduce the costs of transcription. Alternatively, large introns might permit complex regulation, not needed for highly expressed genes. This "genome design" hypothesis evokes a regionalized model of control of expression and hence can explain why intron size covaries with intergene distance, a feature also consistent with the hypothesis that highly expressed genes cluster in genomic regions with high deletion rates. As some genes are expressed in the haploid stage and hence subject to especially strong purifying selection, the evolution of genes in Arabidopsis provides a novel testing ground to discriminate between these possibilities. Importantly, controlling for expression level, genes that are expressed in pollen have shorter introns than genes that are expressed in the sporophyte. That genes flanking pollen-expressed genes have average-sized introns and intergene distances argues against regional mutational biases and genomic design. These observations thus support the view that selection for efficiency contributes to the reduction in intron length and provide the first report of a molecular signature of strong gametophytic selection.
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收藏
页码:154 / 158
页数:5
相关论文
共 30 条
[21]   Transcript profiling in the chl1-5 mutant of Arabidopsis reveals a role of the nitrate transporter NRT1.1 in the regulation of another nitrate transporter, NRT2.1 [J].
Muños, S ;
Cazettes, C ;
Fizames, C ;
Gaymard, F ;
Tillard, P ;
Lepetit, M ;
Lejay, L ;
Gojon, A .
PLANT CELL, 2004, 16 (09) :2433-2447
[22]   Patterns and rates of indel evolution in processed pseudogenes from humans and murids [J].
Ophir, R ;
Graur, D .
GENE, 1997, 205 (1-2) :191-202
[23]   Maximizing the efficacy of SAGE analysis identifies novel transcripts in arabidopsis1[w] [J].
Robinson, SJ ;
Cram, DJ ;
Lewis, CT ;
Parkin, IAP .
PLANT PHYSIOLOGY, 2004, 136 (02) :3223-3233
[24]  
SAITOU N, 1994, MOL BIOL EVOL, V11, P504
[25]   A gene expression map of Arabidopsis thaliana development [J].
Schmid, M ;
Davison, TS ;
Henz, SR ;
Pape, UJ ;
Demar, M ;
Vingron, M ;
Scholkopf, B ;
Weigel, D ;
Lohmann, JU .
NATURE GENETICS, 2005, 37 (05) :501-506
[26]  
UCKER DS, 1984, J BIOL CHEM, V259, P7416
[27]   The signature of selection mediated by expression on human genes [J].
Urrutia, AO ;
Hurst, LD .
GENOME RESEARCH, 2003, 13 (10) :2260-2264
[28]   The human transcriptome map reveals extremes in gene density, intron length, GC content, and repeat pattern for domains of highly and weakly expressed genes [J].
Versteeg, R ;
van Schaik, BDC ;
van Batenburg, MF ;
Roos, M ;
Monajemi, R ;
Caron, H ;
Bussemaker, HJ ;
van Kampen, AHC .
GENOME RESEARCH, 2003, 13 (09) :1998-2004
[29]   Compactness of human housekeeping genes: selection for economy or genomic design? [J].
Vinogradov, AE .
TRENDS IN GENETICS, 2004, 20 (05) :248-253
[30]   Unique features of the plant life cycle and their consequences [J].
Walbot, V ;
Evans, MMS .
NATURE REVIEWS GENETICS, 2003, 4 (05) :369-379