The short-sequence designs of isochores from the human genome

被引:24
作者
Costantini, Maria [1 ]
Bernardi, Giorgio [1 ]
机构
[1] Staz Zool Anton Dohrn, Lab Mol Evolut, I-80121 Naples, Italy
关键词
amino acids; chromatin structure; codon usage; dinucleotides; trinucleotides;
D O I
10.1073/pnas.0803916105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human genome, a typical mammalian genome, is made up of long (approximate to 1-Mb, on average) regions, the isochores, that are fairly homogeneous in base composition and belong in five families characterized by different GC levels. An analysis of di- and tri-nucleotide densities in the isochores from the five families has shown large differences. These different "short-sequence designs:" (i) account for the fractionation of human DNA (and vertebrate DNA in general) when using sequence-specific ligands in density gradients, (ii) are very similar in whole isochores and in the corresponding intergenic sequences and introns, iii) are reflected in different codon usages, (iv) lead to amino acid differences that increase the thermal stability of the proteins encoded by genes located in increasingly GC-rich isochore families, and (v) correspond to different chromatin structures.
引用
收藏
页码:13971 / 13976
页数:6
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