Panaro Maria Antonietta, Calvello Rosa, Miniero Daniela Valeria, Mitolo Vincenzo, Cianciulli Antonia
Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Via Orabona, 4, 70126 Bari, Italy.
Methods Protoc. 2022 Jun 24;5(4):53. doi: 10.3390/mps5040053.
Intron evolution may be readily imaged through the combined use of the "dot plot" function of the NCBI BLAST, aligning two sequences at a time, and the Vertebrate "Multiz" alignment and conservation tool of the UCSC Genome Browser. With the NCBI BLAST, an ideal alignment of two highly conserved sequences generates a diagonal straight line in the plot from the lower left corner to the upper right corner. Gaps in this line correspond to non-conserved sections. In addition, the dot plot of the alignment of a sequence with the same sequence after the removal of the Transposable Elements (TEs) can be observed along the diagonal gaps that correspond to the sites of TE insertion. The UCSC Genome Browser can graph, along the entire sequence of a single gene, the level of overall conservation in vertebrates. This level can be compared with the conservation level of the gene in one or more selected vertebrate species. As an example, we show the graphic analysis of the intron conservation in two genes: the mitochondrial solute carrier 21 (SLC25A21) and the growth hormone receptor (GHR), whose coding sequences are conserved through vertebrates, while their introns show dramatic changes in nucleotide composition and even length. In the SLC25A21, a few short but significant nucleotide sequences are conserved in zebrafish, Xenopus and humans, and the rate of conservation steadily increases from chicken/human to mouse/human alignments. In the GHR, a less conserved gene, the earlier indication of intron conservation is a small signal in chicken/human alignment. The UCSC tool may simultaneously display the conservation level of a gene in different vertebrates, with reference to the level of overall conservation in Vertebrates. It is shown that, at least in SLC25A21, the sites of higher conservation are not always coincident in chicken and zebrafish nor are the sites of higher vertebrate conservation.
通过结合使用NCBI BLAST的“点阵图”功能(一次比对两个序列)以及UCSC基因组浏览器的脊椎动物“多重比对”和保守性工具,可以很容易地描绘内含子的进化情况。使用NCBI BLAST时,两个高度保守序列的理想比对会在图中产生一条从左下角到右上角的对角直线。这条线上的间隙对应于非保守区域。此外,沿着与转座元件(TEs)插入位点相对应的对角间隙,可以观察到一个序列去除TEs后与相同序列比对的点阵图。UCSC基因组浏览器可以绘制单个基因的整个序列上脊椎动物的整体保守水平。这个水平可以与一个或多个选定脊椎动物物种中该基因的保守水平进行比较。例如,我们展示了两个基因内含子保守性的图形分析:线粒体溶质载体21(SLC25A21)和生长激素受体(GHR),它们的编码序列在脊椎动物中是保守的,而它们的内含子在核苷酸组成甚至长度上都有显著变化。在SLC25A21中,一些短但重要的核苷酸序列在斑马鱼、非洲爪蟾和人类中是保守的,保守率从鸡/人与小鼠/人的比对中稳步增加。在GHR这个保守性较低的基因中,内含子保守性的早期迹象是鸡/人比对中的一个小信号。UCSC工具可以同时显示一个基因在不同脊椎动物中的保守水平,并参考脊椎动物的整体保守水平。结果表明,至少在SLC25A21中,鸡和斑马鱼中较高保守位点并不总是一致的,脊椎动物中较高保守位点也不一致。