The Way To Grow To Become Great With PRDX4

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Версія від 09:19, 21 січня 2017, створена Cell0linda (обговореннявнесок) (Створена сторінка: Many complete genomes, including that of Homo sapiens [1, 2], have now been analyzed. On the one hand, our knowledge of genomic and genetic changes is not enoug...)

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Many complete genomes, including that of Homo sapiens [1, 2], have now been analyzed. On the one hand, our knowledge of genomic and genetic changes is not enough to clarify all phenotypic changes in organisms related to natural selection. On the other hand, we showed that vertebrates can be classified into terrestrial and aquatic groups in phylogenetic trees based on Ward��s clustering analysis using amino acid composition or nucleotide content predicted from complete mitochondrial genomes as traits [3, 4]. This result was consistent with that obtained from 16S RNA sequences [3, 4]. Cytochrome C [5], t-RNA [6, 7], 12S RNA [8, 9], 16S RNA [3, 4, 8-10] and 18S RNA genes [11] have been used to construct phylogenetic trees by various analytical methods based on amino acid or nucleotide sequence changes. Although these methods are applicable for single gene(s) or small genome fragments, they are not suitable PRDX4 for DNA Damage inhibitor whole genomes that consist of a huge number of genes. However, using normalization of amino acid compositions or nucleotide contents, we can use whole genomes to compare various organisms. Indeed, biological evolution has been investigated based on cellular amino acid composition obtained from cell hydrolysates [11], and amino acid composition [12] or nucleotide contents [14] predicted from whole genomes. The ratios of amino acids to the total amino acids, or those of nucleotides to the total nucleotides can characterize whole genomes [15], and these indices were used to construct phylogenetic trees [3, 4]. The basis of this concept is the homogenous structure of the genome, composed of small units encoding similar amino acid compositions [13, 14], despite each gene��s different nucleotide sequence. Chargaff��s parity rules [G = C, A = T and (A + G) = (T + C)] are inter and intra molecular rules, and the first and second parity rules represent double DNA strand see more [16] and single DNA strand [17] molecules, respectively. The first parity rule is understandable based on Watson and Crick��s DNA model [18], whereas the second parity rule is not understandable because of the structure of single strand DNA. However, this question was recently solved using a simple mathematical calculation [19]. Mitchell and Bridge showed that Chargaff��s second parity rule is applicable for inter species research using a large data set of whole genomes, and that inter species nucleotide relationships are expressed with linear regression lines [20]. We also showed that inter species nucleotide relationships were expressed with linear regression lines among not only whole genomes but also coding or non-coding regions [21]. In our previous study, we constructed phylogenetic trees based on amino acid composition or nucleotide content as traits, and we classified vertebrates into terrestrial and aquatic groups [3, 4].