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Effect of chimeric relaxin-like gonad-stimulating peptides on oocyte maturation and ovulation in the starfish Asterias rubens and Aphelasterias japonica
被引:9
|作者:
Mita, Masatoshi
[1
,2
]
Elphick, Maurice R.
[3
]
Katayama, Hidekazu
[4
]
机构:
[1] Showa Univ, Dept Biochem, Sch Med, Shinagawa Ku, Hatanodai 8-5-1, Tokyo 1428555, Japan
[2] Waseda Univ, Ctr Adv Biomed Sci, Shinjuku Ku, 2-2 Wakamatsu Cho, Tokyo 1628480, Japan
[3] Queen Mary Univ London, Sch Biol & Chem Sci, Mile End Rd, London E1 4NS, England
[4] Tokai Univ, Sch Engn, Dept Appl Biochem, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 2591292, Japan
关键词:
Relaxin-like gonad-stimulating peptide;
Starfish;
Gonadotropin;
Species-specificity;
Chimeric derivatives;
Receptor;
OVARIAN-FOLLICLE CELLS;
RECEPTOR-BINDING SITE;
ALPHA-S-PROTEINS;
1-METHYLADENINE PRODUCTION;
SWISS-MODEL;
SUBSTANCE;
INVOLVEMENT;
D O I:
10.1016/j.ygcen.2019.113351
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
A relaxin-like gonad-stimulating peptide (RGP), comprising two peptide chains (A- and B-chains) linked by two interchain bonds and one intrachain disulfide bond, acts as a gonadotropin in starfish. RGP orthologs have been identified in several starfish species, including Patiria pectinifera (PpeRGP), Asterias rubens (AruRGP) and Aphelasterias japonica (AjaRGP). To analyze species-specificity, this study examined the effects on oocyte maturation and ovulation in ovaries of A. rubens and A. japonica of nine RGP derivatives comprising different combinations of A- and B-chains from the three species. All nine RGP derivatives induced spawning in A. rubens and A. japonica ovaries. However, AruRGP, AjaRGP and their chimeric derivatives were more potent than peptides containing the A- or B-chain of PpeRGP. Three-dimensional models of the structures of the RGP derivatives revealed that residues in the B-chains, such as Asp(B6), Met(B10) and Phe(B13) in PpeRGP and Glu(B7), Met(B11), and Tyr(B14) in AruRGP and AjaRGP, respectively, are likely to be involved in receptor binding. Conversely, it is likely that Arg(A18) in the A-chain of AruRGP and AjaRGP impairs binding of these peptides to the PpeRGP receptor in P. pectinifera. In conclusion, this study provides new insights into the structural basis of RGP bioactivity and RGP receptor activation in starfish.
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