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首页> 外文期刊>BMC Genomics >The serine/threonine kinase 33 is present and expressed in palaeognath birds but has become a unitary pseudogene in neognaths about 100 million years ago
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The serine/threonine kinase 33 is present and expressed in palaeognath birds but has become a unitary pseudogene in neognaths about 100 million years ago

机译:丝氨酸/苏氨酸激酶33存在于古gna鸟中并在其中表达,但在大约一亿年前的新生neo中已成为单一的假基因

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Background Serine/threonine kinase 33 (STK33) has been shown to be conserved across all major vertebrate classes including reptiles, mammals, amphibians and fish, suggesting its importance within vertebrates. It has been shown to phosphorylate vimentin and might play a role in spermatogenesis and organ ontogenesis. In this study we analyzed the genomic locus and expression of stk33 in the class Aves, using a combination of large scale next generation sequencing data analysis and traditional PCR. Results Within the subclass Palaeognathae we analyzed the white-throated tinamou (Tinamus guttatus), the African ostrich (Struthio camelus) and the emu (Dromaius novaehollandiae). For the African ostrich we were able to generate a 62,778?bp long genomic contig and an mRNA sequence that encodes a protein showing highly significant similarity to STK33 proteins from other vertebrates. The emu has been shown to encode and transcribe a functional STK33 as well. For the white-throated tinamou we were able to identify 13 exons by sequence comparison encoding a protein similar to STK33 as well. In contrast, in all 28 neognath birds analyzed, we could not find evidence for the existence of a functional copy of stk33 or its expression. In the genomes of these 28 bird species, we found only remnants of the stk33 locus carrying several large genomic deletions, leading to the loss of multiple exons. The remaining exons have acquired various indels and premature stop codons. Conclusions We were able to elucidate and describe the genomic structure and the transcription of a functional stk33 gene within the subclass Palaeognathae, but we could only find degenerate remnants of stk33 in all neognath birds analyzed. This led us to the conclusion that stk33 became a unitary pseudogene in the evolutionary history of the class Aves at the paleognath-neognath branch point during the late cretaceous period about 100 million years ago. We hypothesize that the pseudogenization of stk33 might have become fixed in neognaths due to either genetic redundancy or a non-orthologous gene displacement and present potential candidate genes for such an incident.
机译:背景技术丝氨酸/苏氨酸激酶33(STK33)在所有主要的脊椎动物种类(包括爬行动物,哺乳动物,两栖动物和鱼类)中均被保守,这表明其在脊椎动物中的重要性。已经显示它可以使波形蛋白磷酸化,并可能在精子发生和器官本体发生中起作用。在这项研究中,我们结合了大规模下一代测序数据分析和传统PCR技术,分析了Aves类中stk33的基因组基因座和表达。结果我们在古颚类亚类中分析了白喉的Tinamou(Tinamus guttatus),非洲鸵鸟(Struthio camelus)和and(Dromaius novaehollandiae)。对于非洲鸵鸟,我们能够产生一个62,778?bp长的基因组重叠群和一个mRNA序列,该序列编码一种蛋白质,该蛋白质与来自其他脊椎动物的STK33蛋白质显示出非常重要的相似性。 mu已被证明还能编码和转录功能性STK33。对于白喉的犬科动物,我们还能够通过序列比较识别出一种编码与STK33类似的蛋白质的外显子。相反,在所有28只被分析的新生鸟中,我们找不到stk33功能性拷贝或其表达的存在的证据。在这28种鸟类的基因组中,我们仅发现stk33基因座的残基带有几个大的基因组缺失,从而导致多个外显子的丢失。其余的外显子已经获得了各种插入缺失和过早的终止密码子。结论我们能够阐明和描述古猿亚目内一个功能性stk33基因的基因组结构和转录,但是我们只能在所有被分析的新生鸟类中找到stk33的简并残基。这导致我们得出这样的结论:在大约1亿年前的白垩纪晚期,stk33在古白垩纪-新白垩纪分支点的Aves类进化史中成为一个单一的假基因。我们假设,由于遗传冗余或非直系同源基因置换,stk33的假基因可能已固定在新生中,并提出了此类事件的潜在候选基因。

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