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首页> 外文期刊>Evolutionary Bioinformatics >Evolutionary Analysis of Makorin Ring Finger Protein 3 Reveals Positive Selection in Mammals
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Evolutionary Analysis of Makorin Ring Finger Protein 3 Reveals Positive Selection in Mammals

机译:Makorin Ring Finger蛋白3的进化分析显示哺乳动物的阳性选择

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Makorin ring finger proteins (MKRNs) are part the of ubiquitin-proteasome system; a complex system important for cell functions. Ubiquitin fate through proteolytic, non-proteolytic pathways varies, depending on covalent linkage between ubiquitin and protein substrates. Makorin ring finger protein 3 is an integral part of covalent linkage of ubiquitin to protein substrates. Similar to others imprinted genes, MKRN3 also evolve under positive selection; however, which codons are specifically selected in MKRN3 during evolution are needed to be explored. Different maximum-likelihood (ML) codon-based methodologies were used to ascertain positive selection signatures in 22 mammalian sequences of MKRN3 to probe an individual codon for positive selection signatures. By applying the HyPhy software package implemented in the Data Monkey Web Server and CODEML implemented in PAML, evolutionary analysis based on two Ml frameworks were conducted. The analysis was executed by comparing M1a against M2a, M7 against M8, and PAML models and 2?Lnl (LRT) was resulted by likelihood logs. M1a contributed ω1 (dN/dS) with LRT value (?Lnl) 12.01, and positive selection was found in M2a with ω3=2.23603. To further improve selection test, M8 was compared to M7 with 2?Lnl (LRT) 30.17, and M8 showed positive selection with ω=1.55759. The data were fit to M8 than M7, which suggests that M8 was the most significant model of selection. M8 was judged encouraging for this analysis and used to establish a positive selection of MKRN3 proteins. We found Gly312 as a positively selected amino acid in a zinc finger motif/Really Interesting New Gene (RING) finger motif; the former ones’ region is involved in RNA binding and the later ones in ubiquitin ligase activity of the protein, vital for protein function. Selection analyses of MKRNs might advance the developments in unique approaches that could lead to genetic progress over the selection of superior individuals with the breeding values higher for certain traits as ancestries to get the next generation.
机译:Makorin戒指手指蛋白(MKRNS)是泛素 - 蛋白酶体系的一部分;一个复杂的系统对于细胞功能很重要。通过蛋白水解,非蛋白水解途径的泛素命运,取决于泛素和蛋白质底物之间的共价键。 Makorin环手指蛋白3是泛素与蛋白质底物的共价连接的一个组成部分。与其他印迹基因类似,MKRN3也在阳性选择下进化;然而,需要在进化期间在MKRN3中专门选择该密码子。不同的最大可能性(ML)基于密码子的方法用于确定MKRN3的22例哺乳动物序列中的阳性选择签名,以探测各个密码子以进行正选择签名。通过应用在PAML中实现的数据猴子Web服务器和Codeml中实现的剪钥软件包,进行了基于两个ML框架的进化分析。通过将M1A与M2a,M7对M8进行比较来执行分析,并通过似然日志导致PAML模型和2?LNL(LRT)。 M1a贡献ω1(dn / ds)与lrt值(Δln1)12.01,在M2a中发现阳性选择,ω3= 2.23603。为了进一步改善选择试验,将M8与2·LNL(LRT)30.17的M7进行比较,M8显示ω= 1.55759的阳性选择。数据适用于M8而不是M7,这表明M8是最重要的选择模型。 M8被判断为该分析令人鼓舞,并用于建立MKRN3蛋白的阳性选择。我们发现Gly312作为锌手指基序/真正有趣的新基因(环)手指基序的正选氨基酸;前者的区域涉及RNA结合和后来的蛋白质蛋白质连接酶活性,对蛋白质功能至关重要。 MKRNS的选择分析可能会提高独特方法的发展,这可能导致遗传进展在选择优越个体上,育种价值较高,因为某些特征作为祖先以获得下一代。

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