虹鳟(Oncorhynchus mykiss)卵黄原蛋白位点的基因组分析揭示了基因扩增和反转录子活性的复杂历史。

V Trichet, N Buisine, N Mouchel, P Morán, A M Pendás, J P Le Pennec, J Wolff
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引用次数: 70

摘要

卵黄原蛋白(Vitellogenins, Vtg)是大多数卵生生物的主要卵黄蛋白。它们是由少数基因编码的——根据物种的不同,在1到4个基因之间。然而,虹鳟鱼基因组中Vtg区域的特征显示出不同寻常的特征,该位点包含20个完整基因和10个假基因。尽管在序列水平上,Vtg基因表现出高度的相似性,但由于插入、删除和重排事件,它们彼此不同。荧光原位杂交(FISH)、脉冲场凝胶电泳(PFGE)和Southern分析表明,所有基因拷贝都包含在一个1500 -kb的区域内,大多数基因形成串联阵列,由一个保守的4.5 kb的基因间区隔开。大型重复碎片的存在表明该区域遭受了几次扩增事件。Vtg内含子9中的反转录子元件(称为19)的存在似乎是导致10个假基因中至少9个沉默的原因。另外两个不完全反转录转座子(一个LTR型和一个line型)和来自hiv样逆转录病毒的序列被插入到非常靠近转录起始位点的保守基因间区。它们在vtg5 '侧的所有区域都存在,这表明它们可能在该位点的基因扩增中起作用。
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Genomic analysis of the vitellogenin locus in rainbow trout (Oncorhynchus mykiss) reveals a complex history of gene amplification and retroposon activity.

Vitellogenins (Vtg) are the major yolk proteins in most oviparous organisms. They are encoded by a small number of genes--between one and four depending on the species. Characterization of the Vtg region in the genome of the rainbow trout reveals unusual features, however, in that this locus contains twenty complete genes and ten pseudogenes per haploid genome. The Vtg genes differ from each other by insertion, deletion and rearrangement events, although, at the sequence level, they show a high degree of similarity. Fluorescent in situ hybridization (FISH), pulsed-field gel electrophoresis (PFGE) and Southern analysis indicate that all gene copies are contained in a single 1,500-kb region, and that most of the genes form tandem arrays separated by a conserved 4.5-kb intergenic region. The presence of large reiterated fragments indicates that this region has been subjected to several amplification events. The presence of a retroposon element (called 19) in Vtg intron 9 appears to be responsible for the silencing of at least nine of the ten pseudogenes. Two other incomplete retrotransposons (one LTR- and one LINE-type) and sequences derived from a HIV-like retrovirus are inserted into the conserved intergenic region, very close to the transcription start site. Their presence in all Vtg 5'-flanking regions suggests a possible role in gene amplification at this locus.

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