Molecular identification and expression analysis of natural resistance associated macrophage protein (Nramp) cDNA from Japanese flounder (Paralichthys olivaceus)

被引:13
|
作者
Chen, SL [1 ]
Wang, ZJ
Xu, MY
Gui, JF
机构
[1] Chinese Acad Fisheries Sci, Yellow Sea Fisheries Res Inst, Minist Agr, Key Lab Sustainable Utilizat Marine Fisheries Res, Qingdao 266071, Peoples R China
[2] Shanghai Fisheries Univ, E Inst Shanghai Univ, Aquaculture Div, Shanghai 200090, Peoples R China
[3] Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
[4] Chinese Acad Sci, Inst Hydrobiol, Wuhan Ctr Dev Biol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Peoples R China
关键词
Japanese flounder; Paralichthys olivaceus; Nramp; cDNA; expression;
D O I
10.1016/j.fsi.2005.05.011
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Natural resistance associated macrophage protein (Nramp) controls partially innate resistance to intracellular parasites. Its function is to enhance the ability of macrophages to kill pathogens. However, little is known about the structure and function of Nramp in lower vertebrates such as teleosts. We have recently isolated a cDNA encoding Nramp from Japanese flounder (Paratichthys olivaceus). The full-length cDNA of the Nramp is 3066 bp in length, including 224 bp 5' terminal UTR, 1662 bp encoding region and 1180 bp 3' terminal UTR. The 1662-nt open reading frame was found to code for a protein with 554 amino acid residues. Comparison of amino acid sequence indicated that Japanese flounder Nramp consists of 12 transmembrane (TM) domains. A consensus transport motif (CTM) containing 20 residues was observed between transmembrane domains 8 and 9. The deduced amino acid sequence of Japanese flounder had 77.30%, 82.71%, 82.67%, 79.64%, 80.72%, 90.97%, 91.16%, 60.14%, 71.48%, 61.69%, 72.37% identity with that of rainbow trout Nramp alpha and beta, channel catfish Nramp, fathead minnow Nramp, common carp Nramp, striped sea bass Nramp, red sea bream Nramp, mouse Nramp 1 and 2, human Nramp 1 and 2, respectively. RT-PCR indicated that Nramp transcripts were highly abundant in spleen, head kidney, abundant in intestine, liver and gill, and less abundant in heart. The level of Nramp mRNA in embryos gradually increases during embryogenesis from 4 h (8 cell stage) to 80 h (hatched stage) after fertilization. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:365 / 373
页数:9
相关论文
共 50 条
  • [1] Cloning and analysis of expression of Mx cDNA in Japanese flounder, Paralichthys olivaceus
    Lee, JY
    Hirono, I
    Aoki, T
    DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2000, 24 (04): : 407 - 415
  • [2] Molecular analysis of complement regulatory protein-like cDNA from the Japanese flounder Paralichthys olivaceus
    Katagiri, T
    Hirono, I
    Aoki, T
    FISHERIES SCIENCE, 1998, 64 (01) : 140 - 143
  • [3] Molecular cloning and sequence analysis of transferrin cDNA from Japanese flounder Paralichthys olivaceus
    Kim, YD
    Lee, JY
    Hong, YK
    Hikima, J
    Hirono, I
    Aoki, T
    FISHERIES SCIENCE, 1997, 63 (04) : 582 - 586
  • [4] Molecular cloning, characterization and expression analysis of natural resistance associated macrophage protein (Nramp) cDNA from turbot (Scophthalmus maximus)
    Chen, Song-Lin
    Zhang, Yu-Xi
    Xu, Jian-Yong
    Meng, Liang
    Sha, Zhen-Xia
    Ren, Guo-Cheng
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2007, 147 (01): : 29 - 37
  • [5] cDNA clone and expression analysis of α-Tropomyosin during Japanese flounder(Paralichthys olivaceus) metamorphosis
    Hong-Mei ZHANG
    Yan-Fang SU
    Zhi-Yi SHI
    Yuan-Shuai FU
    Zoological Research, 2014, 35 (04) : 307 - 312
  • [6] Identification and characterization of a fish natural resistance-associated macrophage protein (NRAMP) cDNA
    Saeij, JPJ
    Wiegertjes, GF
    Stet, RJM
    IMMUNOGENETICS, 1999, 50 (1-2) : 60 - 66
  • [7] Identification and characterization of a fish natural resistance-associated macrophage protein (NRAMP) cDNA
    Jeroen P. J. Saeij
    G. F. Wiegertjes
    René J. M. Stet
    Immunogenetics, 1999, 50 : 60 - 66
  • [8] Identification and expression analysis of IGFBP-1 gene from Japanese flounder (Paralichthys olivaceus)
    Zhai, Wanying
    Zhang, Junling
    Shi, Zhiyi
    Fu, Yuanshuai
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2012, 161 (04): : 413 - 420
  • [9] Characterization and expression of c-type lysozyme cDNA from Japanese flounder (Paralichthys olivaceus)
    Hikima, J
    Hirono, I
    Aoki, T
    MOLECULAR MARINE BIOLOGY AND BIOTECHNOLOGY, 1997, 6 (04) : 339 - 344
  • [10] Identification and expression analysis of suppressors of cytokine signaling (SOCS) of Japanese flounder Paralichthys olivaceus
    Thanasaksiri, Kittipong
    Hirono, Ikuo
    Kondo, Hidehiro
    FISH & SHELLFISH IMMUNOLOGY, 2016, 58 : 145 - 152