Quezada-Díaz Jorge Ernesto, Muliyil Taniya, Río Javier, Betrán Esther
Department of Biology, University of Texas at Arlington, Box 19498, Arlington, TX 76019, USA.
Genetica. 2010 Oct;138(9-10):925-37. doi: 10.1007/s10709-010-9474-8. Epub 2010 Aug 8.
Gene duplication is a major force driving genome evolution, and examples of this mode of evolution and of the functions of duplicated genes are needed to reveal general patterns. Here, our study focuses on a particular retrogene (i.e., CG9573) that originated about 5-13 million years ago that we have named Drcd-1 related. It originated in Drosophila through retroposition of the parental gene Required for cell differentiation 1 of Drosophila (Drcd-1; CG14213), which is a known transcription cofactor. Drcd-1r is only present in D. melanogaster, D. simulans, D. sechellia, and D. mauritiana. Drcd-1r is an X to autosome retroposition event. Many retrogenes are X to autosome copies and it has been shown that positive selection underlies this bias. We sought to understand Drcd-1r mode of evolution and function to contribute to the understanding of the selective pressures acting on X to autosome retrogenes. Drcd-1r overlaps with another gene, it is within the 3' UTR of the gene CG13102 and is encoded in the opposite orientation. We have studied the characteristics of the transcripts and quantified expression of CG13102 and Drcd-1r in wild-type flies. We found that Drcd-1r is transcribed specifically in testes. We also studied the molecular evolution of Drcd-1r and Drcd-1 and found that the parental gene has evolved under very strong purifying selection but the retrogene has evolved very rapidly (Ka/Ks ~1) under both positive and purifying selection, as revealed using divergence and polymorphism data. These results indicate that Drcd-1r has a novel function in the Drosophila testes. To further explore Drcd-1r function we used a strain containing a P element inserted in the region where CG13102 and Drcd-1r are located that shows recessive male sterility. Analysis of this strain reveals the difficulties that can be encountered in studying the functions of genes with overlapping transcripts. Avenues for studying of the function of this gene are proposed.
基因复制是推动基因组进化的主要力量,需要这种进化模式以及复制基因功能的实例来揭示一般模式。在这里,我们的研究聚焦于一个约在500万至1300万年前起源的特定反转录基因(即CG9573),我们将其命名为Drcd-1相关基因。它通过果蝇细胞分化所需的亲本基因1(Drcd-1;CG14213)的反转录插入起源于果蝇,Drcd-1是一种已知的转录辅因子。Drcd-1r仅存在于黑腹果蝇、拟果蝇、塞舌尔果蝇和毛里求斯果蝇中。Drcd-1r是从X染色体到常染色体的反转录事件。许多反转录基因都是从X染色体到常染色体的拷贝,并且已经表明正选择是这种偏向的基础。我们试图了解Drcd-1r的进化模式和功能,以有助于理解作用于从X染色体到常染色体的反转录基因的选择压力。Drcd-1r与另一个基因重叠,它位于基因CG13102的3'非翻译区内,并且以相反的方向编码。我们研究了转录本的特征,并对野生型果蝇中CG13102和Drcd-1r的表达进行了定量。我们发现Drcd-1r仅在睾丸中特异性转录。我们还研究了Drcd-1r和Drcd-1的分子进化,发现亲本基因在非常强的纯化选择下进化,但反转录基因在正选择和纯化选择下都进化得非常快(Ka/Ks约为1),这是通过分歧和多态性数据揭示的。这些结果表明Drcd-1r在果蝇睾丸中具有新功能。为了进一步探索Drcd-1r的功能,我们使用了一个含有插入在CG13102和Drcd-1r所在区域的P因子的品系,该品系表现出隐性雄性不育。对该品系的分析揭示了在研究具有重叠转录本的基因功能时可能遇到的困难。提出了研究该基因功能的途径。