How similar are amino acid mutations in human genetic diseases and evolution

被引:16
|
作者
Wu, Hao
Ma, Bin-Guang
Zhao, Ji-Tao
Zhang, Hong-Yu [1 ]
机构
[1] Shandong Univ Technol, Ctr Adv Study, Shandong Prov Res Ctr Bioinformat Engn & Tech, Zibo 255049, Peoples R China
[2] Suzhou Univ, Coll Chem & Chem Engn, Suzhou 215006, Peoples R China
关键词
genetic diseases; deleterious mutation; evolution; RESISTANCE; PATHOLOGY; SELECTION; DEAFNESS;
D O I
10.1016/j.bbrc.2007.07.141
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulating evidence indicates that some deleterious mutations responsible for genetic diseases may offer benefits for human to prevent other diseases. Therefore, human genetic diseases and evolution were tentatively regarded as the two sides of the same coin, which stimulated our interest to explore how similar are amino acid mutations in human genetic diseases and evolution. Through a large-scale analysis on amino acid mutation patterns of genetic diseases and evolution of Hominidae (Homo sapiens and Pan troglodytes), it was found that there exist significant correlations between two mutation patterns. Besides, there also exist some evident differences between both mutations, especially those associated with four amino acids C, G, R, and L. These findings are of significance to understanding the subtle connections between human genetic diseases and evolution. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:233 / 237
页数:5
相关论文
共 50 条
  • [41] CURRENT NEWS ON AMINO ACID DISEASES
    FARRIAUX, JP
    LILLE MEDICAL, 1971, 16 (02): : 342 - &
  • [42] PDGF receptor mutations in human diseases
    Guerit, Emilie
    Arts, Florence
    Dachy, Guillaume
    Boulouadnine, Boutaina
    Demoulin, Jean-Baptiste
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2021, 78 (08) : 3867 - 3881
  • [43] Human evolution, human brain diseases
    Diaconeasa, A. G.
    Spiru, L.
    Turcu, I.
    INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2010, 28 (08) : 705 - 705
  • [44] OLIGONUCLEOTIDE-AMINO ACID BINDING INTERACTIONS - APPROACH TO STUDY OF EVOLUTION OF GENETIC CODE
    SAXINGER, C
    SOGIN, M
    WOESE, C
    PONNAMPE.C
    FEDERATION PROCEEDINGS, 1972, 31 (02) : A902 - &
  • [45] Determining amino acid scores of the genetic code table: Complementarity, structure, function and evolution
    Stambuk, Nikola
    Konjevoda, Pasko
    BIOSYSTEMS, 2020, 187
  • [46] PDGF receptor mutations in human diseases
    Emilie Guérit
    Florence Arts
    Guillaume Dachy
    Boutaina Boulouadnine
    Jean-Baptiste Demoulin
    Cellular and Molecular Life Sciences, 2021, 78 : 3867 - 3881
  • [47] Human diseases associated with connexin mutations
    Srinivas, Miduturu
    Verselis, Vytas K.
    White, Thomas W.
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2018, 1860 (01): : 192 - 201
  • [48] Relationship between amino acid usage and amino acid evolution in primates
    Liu, Haoxuan
    Xie, Zhengqing
    Tan, Shengjun
    Zhang, Xiaohui
    Yang, Sihai
    GENE, 2015, 557 (02) : 182 - 187
  • [49] HOW DIFFERENT AMINO-ACID-SEQUENCES DETERMINE SIMILAR PROTEIN STRUCTURES - STRUCTURE AND EVOLUTIONARY DYNAMICS OF THE GLOBINS
    LESK, AM
    CHOTHIA, C
    JOURNAL OF MOLECULAR BIOLOGY, 1980, 136 (03) : 225 - &
  • [50] Zebrafish: A Powerful Model for Understanding the Functional Relevance of Noncoding Region Mutations in Human Genetic Diseases
    Mann, Anita
    Bhatia, Shipra
    BIOMEDICINES, 2019, 7 (03)