Exon structure conservation despite low sequence similarity:: a relic of dramatic events in evolution?

被引:89
作者
Betts, MJ
Guigó, R
Agarwal, P
Russell, RB
机构
[1] GlaxoSmithKline Inc, Bioinformat, Harlow CM19 5AW, Essex, England
[2] IMIM UPF, Res Grp Biomed Informat, Barcelona 08003, Spain
[3] GlaxoSmithKline Inc, Bioinformat, King Of Prussia, PA 19406 USA
[4] European Mol Biol Lab, D-69012 Heidelberg, Germany
关键词
evolution; exon; immune system; intron; protein structure;
D O I
10.1093/emboj/20.19.5354
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 evolutionary significance of introns remains a mystery. The current availability of several complete eukaryotic genomes permits new studies to probe the possible function of these peculiar genomic features. Here we investigate the degree to which gene structure (intron position, phase and length) is conserved between homologous protein domains. We find that for certain extracellular-signalling and nuclear domains, gene structures are similar even when protein sequence similarity is low or not significant and sequences can only be aligned with a knowledge of protein tertiary structure. In contrast, other domains, including most intracellular signalling modules, show little gene structure conservation. Intriguingly, many domains with conserved gene structures, such as cytokines, are involved in similar biological processes, such as the immune response. This suggests that gene structure conservation may be a record of key events in evolution, such as the origin of the vertebrate immune system or the duplication of nuclear receptors in nematodes. The results suggest ways to detect new and potentially very remote homologues, and to construct phylogenies for proteins with limited sequence similarity.
引用
收藏
页码:5354 / 5360
页数:7
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