Tracing and exploring the evolutionary origin and systematic function of fish complement C9

被引:0
|
作者
Lisen Li
Yubang Shen
Xiaoyan Xu
Weining Yang
Jiale Li
机构
[1] Shanghai Ocean University,Key Laboratory of Freshwater Aquatic Genetic Resources, Ministry of Agriculture and Rural Affairs, College of Aquaculture and Life Science
[2] Shanghai Ocean University,Shanghai Engineering Research Center of Aquaculture
来源
关键词
Complement C9; Gene element; Immunity; Pathway analysis;
D O I
暂无
中图分类号
学科分类号
摘要
Complement C9, as a member of terminal complement component (TCC) protein, plays important roles in innate immunity. However, some complement components appear to show difference and evolutionary complexity between higher and lower vertebrates. Hence, it is essential to carry on a study of evolutionary origin and systematic function of C9 in fish and non-fish vertebrates. This study aims to explore the complement gene evolution and potential function in fish based on molecular and structural biology. Herein, we found complete divergence of C9 throughout the gene evolution. The optimal codons of C9 sequences tended to be closer to the genomes of lower vertebrates compared to higher vertebrates. Further, conserved amino acids in the C9 TMH1 region were identified, implying their potential functional association with MAC growth and pore formation. Transposons and simple repeats, as gene elements, exhibited a differential distribution in the genomic regions in different animal groups but were sparsely scattered around the sixth exon (TMH1 region). Notably, this demonstrated the regulatory complexity of the C9 gene in higher vertebrates. The negative selection pressures on fish and non-fish groups improved both the sequence conservation and similarity. Through gene/protein regulatory network and pathway analyses, the systematic function of C9 protein was showcased; thus, we could reveal the divergence of the systematic function of C9 across species from different evolutionary positions. In addition, more complicated functions of C9 in higher vertebrates could established by the altered spatial conformation of the protein. Collectively, the present study illustrates the C9 gene evolutionary process and the difference in its systematic function across multiple species. Such advances provide new insights for understanding the evolutionary and potential functions of complement C9.
引用
收藏
页码:665 / 676
页数:11
相关论文
共 50 条
  • [31] A BIOTIN-AVIDIN SANDWICH ELISA FOR QUANTIFICATION OF INTACT COMPLEMENT COMPONENT C9 - THE SERA FROM HEREDITARY C9 DEFICIENT INDIVIDUALS COMPLETELY LACK C9
    TAKATA, Y
    MORIYAMA, T
    FUKUMORI, Y
    YODEN, A
    SHIMA, M
    INAI, S
    JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 117 (01) : 107 - 113
  • [32] MONOCLONAL-ANTIBODIES AND THE STRUCTURE OF COMPLEMENT COMPONENT C9
    LUZIO, JP
    JACKSON, P
    CAMPBELL, AK
    MORGAN, BP
    STANLEY, KK
    BIOCHEMICAL SOCIETY TRANSACTIONS, 1985, 13 (01) : 105 - 106
  • [33] THE SEQUENCE AND TOPOLOGY OF HUMAN-COMPLEMENT COMPONENT C9
    STANLEY, KK
    KOCHER, HP
    LUZIO, JP
    JACKSON, P
    TSCHOPP, J
    EMBO JOURNAL, 1985, 4 (02): : 375 - 382
  • [34] Heterogeneity in the genetic basis of human complement C9 deficiency
    Witzel-Schlömp, K
    Hobart, MJ
    Fernie, BA
    Orren, A
    Würzner, R
    Rittner, C
    Kaufmann, T
    Schneider, PM
    IMMUNOGENETICS, 1998, 48 (02) : 144 - 147
  • [35] Heterogeneity in the genetic basis of human complement C9 deficiency
    Konstanze Witzel-Schlömp
    Michael J. Hobart
    Barbara A. Fernie
    Ann Orren
    Reinhard Würzner
    Christian Rittner
    Thomas Kaufmann
    P. M. Schneider
    Immunogenetics, 1998, 48 : 144 - 147
  • [36] A MECHANISM FOR THE INSERTION OF COMPLEMENT COMPONENT C9 INTO TARGET MEMBRANES
    STANLEY, KK
    PAGE, M
    CAMPBELL, AK
    LUZIO, JP
    MOLECULAR IMMUNOLOGY, 1986, 23 (05) : 451 - 458
  • [37] Deposition of complement C9 in primary sclerosing cholangitis (PSC).
    Shanahan, J
    Rosenberg, W
    Chapman, RW
    Fleming, KA
    GASTROENTEROLOGY, 1998, 114 (04) : A1340 - A1340
  • [38] MEMBRANOLYSIS BY ISOLATED C9 IN THE ABSENCE OF OTHER COMPLEMENT PROTEINS
    TSCHOPP, J
    PODACK, ER
    MULLEREBERHARD, HJ
    MOLECULAR IMMUNOLOGY, 1982, 19 (11) : 1407 - 1407
  • [39] Complement component C9 (C9) potentiates the protective effect of cefotaxime in neonatal rats septic with E-coli.
    Jung, E
    Walz, BM
    Drehs, MM
    Feldhoff, RC
    Lassiter, HA
    PEDIATRIC RESEARCH, 1996, 39 (04) : 1759 - 1759
  • [40] Expression of complement C4 and C9 genes by human astrocytes
    Walker, DG
    Kim, SU
    McGeer, PL
    BRAIN RESEARCH, 1998, 809 (01) : 31 - 38