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硬骨鱼类孵化酶基因的内含子丢失进化。

Intron-loss evolution of hatching enzyme genes in Teleostei.

机构信息

Atmosphere and Ocean Research Institute, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8564, Japan.

出版信息

BMC Evol Biol. 2010 Aug 27;10:260. doi: 10.1186/1471-2148-10-260.

Abstract

BACKGROUND

Hatching enzyme, belonging to the astacin metallo-protease family, digests egg envelope at embryo hatching. Orthologous genes of the enzyme are found in all vertebrate genomes. Recently, we found that exon-intron structures of the genes were conserved among tetrapods, while the genes of teleosts frequently lost their introns. Occurrence of such intron losses in teleostean hatching enzyme genes is an uncommon evolutionary event, as most eukaryotic genes are generally known to be interrupted by introns and the intron insertion sites are conserved from species to species. Here, we report on extensive studies of the exon-intron structures of teleostean hatching enzyme genes for insight into how and why introns were lost during evolution.

RESULTS

We investigated the evolutionary pathway of intron-losses in hatching enzyme genes of 27 species of Teleostei. Hatching enzyme genes of basal teleosts are of only one type, which conserves the 9-exon-8-intron structure of an assumed ancestor. On the other hand, otocephalans and euteleosts possess two types of hatching enzyme genes, suggesting a gene duplication event in the common ancestor of otocephalans and euteleosts. The duplicated genes were classified into two clades, clades I and II, based on phylogenetic analysis. In otocephalans and euteleosts, clade I genes developed a phylogeny-specific structure, such as an 8-exon-7-intron, 5-exon-4-intron, 4-exon-3-intron or intron-less structure. In contrast to the clade I genes, the structures of clade II genes were relatively stable in their configuration, and were similar to that of the ancestral genes. Expression analyses revealed that hatching enzyme genes were high-expression genes, when compared to that of housekeeping genes. When expression levels were compared between clade I and II genes, clade I genes tends to be expressed more highly than clade II genes.

CONCLUSIONS

Hatching enzyme genes evolved to lose their introns, and the intron-loss events occurred at the specific points of teleostean phylogeny. We propose that the high-expression hatching enzyme genes frequently lost their introns during the evolution of teleosts, while the low-expression genes maintained the exon-intron structure of the ancestral gene.

摘要

背景

孵化酶属于天冬氨酸金属蛋白酶家族,可在胚胎孵化时分解卵壳。该酶的同源基因存在于所有脊椎动物的基因组中。最近,我们发现四足动物的基因外显子-内含子结构是保守的,而鱼类的基因经常失去内含子。在鱼类孵化酶基因中发生这种内含子丢失是一种不常见的进化事件,因为大多数真核基因通常被认为是由内含子打断的,并且物种间的内含子插入位点是保守的。在这里,我们报告了对鱼类孵化酶基因的外显子-内含子结构的广泛研究,以深入了解内含子在进化过程中是如何以及为何丢失的。

结果

我们研究了 27 种硬骨鱼孵化酶基因的内含子丢失的进化途径。基础硬骨鱼的孵化酶基因只有一种类型,保留了假定祖先的 9 外显子-8 内含子结构。另一方面,鳐形目和真骨鱼类拥有两种类型的孵化酶基因,这表明鳐形目和真骨鱼类的共同祖先发生了基因复制事件。基于系统发育分析,将复制的基因分为两个分支,分支 I 和分支 II。在鳐形目和真骨鱼类中,分支 I 基因形成了一种特定于系统发育的结构,例如 8 外显子-7 内含子、5 外显子-4 内含子、4 外显子-3 内含子或无内含子结构。与分支 I 基因相比,分支 II 基因的结构在其配置上相对稳定,并且与祖先基因相似。表达分析表明,孵化酶基因与管家基因相比是高表达基因。当比较分支 I 和 II 基因的表达水平时,分支 I 基因的表达水平往往高于分支 II 基因。

结论

孵化酶基因进化失去了内含子,内含子丢失事件发生在硬骨鱼系统发育的特定点上。我们提出,在硬骨鱼的进化过程中,高表达的孵化酶基因经常失去内含子,而低表达的基因则保持了祖先基因的外显子-内含子结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7582/2939575/02b77f920465/1471-2148-10-260-1.jpg

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