Identification, cloning and expression analysis of Catechol-O-methyltransferase (COMT) gene from shrimp, Penaeus monodon and its relevance to salinity stress

被引:17
作者
Rajesh, S. [1 ]
Kiruthika, J. [1 ]
Ponniah, A. G. [1 ]
Shekhar, M. S. [1 ]
机构
[1] Cent Inst Brackishwater Aquaculture 75, Genet & Biotechnol Unit, Madras 600028, Tamil Nadu, India
关键词
COMT; Penaeus monodon; Salinity stress; BRANCHIAL CARBONIC-ANHYDRASE; EURYHALINE GREEN CRAB; LITOPENAEUS-VANNAMEI; CARCINUS-MAENAS; WHITE SHRIMP; CDNA; TEMPERATURE; OSMOLALITY; INDUCTION; HEMOLYMPH;
D O I
10.1016/j.fsi.2012.01.015
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
O-methyltransferase (OMT), a protein present ubiquitously in wide range of organisms plays significant role in methylation of small macro molecules for various functional and regulatory purposes. In crustaceans, OMT has functional role in growth, reproduction, ovarian development and molting. In the present study, suppression subtractive hybridization (SSH) performed using gill tissues of low (3ppt) and high (55ppt) salinity stressed shrimp Penaeus monodon resulted in identification of differentially expressed genes involved in signal transduction pathways, metabolism, defense proteins, DNA repair and synthesis, apoptosis, cell cycle regulation along with unknown and hypothetical proteins. Catechol-O-methyltransferase (COMT) a type of OMT was identified by SSH as one of the differentially expressed genes of shrimp P. monodon subjected to low and high salinity stress. The full length cDNA of COMT was cloned from the gills of P. monodon which consisted an open reading frame of 666 bp, encoding 221 amino acids. The ORF revealed one each of N-glycosylation and O-glycosylation sites and nine phosphorylation sites. The deduced amino acid sequence of COMT exhibited high sequence identity (92%) with COMT class of protein from Fenneropenaeus chinensis. Real time PCR analysis of the shrimp samples exposed to low salinity conditions at 3ppt revealed significant increase in expression of COMT transcripts in the guts at 24 h, 48 h, 1 week and 2 weeks, gills at 24 h and in the muscle tissues at 48 h, with maximum expression of the COMT levels by 5 fold in guts (1 week), 1 fold in gills (24 h) and 1.5 fold in muscle (48 h) respectively. The increased expression level of COMT at different time intervals in different tissues suggests a possible role of this gene in salinity stress tolerance in shrimps under low salinity conditions. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:693 / 699
页数:7
相关论文
共 35 条
  • [1] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [2] Kinetics of rat brain and liver solubilized membrane-bound catechol-O-methyltransferase
    Bonifácio, MJ
    Vieira-Coelho, MA
    Borges, N
    Soares-da-Silva, P
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 384 (02) : 361 - 367
  • [3] Adaptation of the black tiger shrimp, Penaeus monodon, to different salinities through an excretory function of the antennal gland
    Buranajitpirom, Decha
    Asuvapongpatana, Somluk
    Weerachatyanukul, Wattana
    Wongprasert, Kanokpan
    Namwong, Wisa
    Poltana, Pisit
    Withyachumnarnkul, Boonsirm
    [J]. CELL AND TISSUE RESEARCH, 2010, 340 (03) : 481 - 489
  • [4] SURVIVAL, HEMOLYMPH OSMOLALITY AND TISSUE WATER OF PENAEUS-CHINENSIS JUVENILES ACCLIMATED TO DIFFERENT SALINITY AND TEMPERATURE LEVELS
    CHEN, JC
    LIN, MN
    TING, YY
    LIN, JN
    [J]. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 1995, 110 (03): : 253 - 258
  • [5] OSMOLALITY AND CHLORIDE CONCENTRATION IN THE HEMOLYMPH OF SUBADULT PENAEUS-CHINENSIS SUBJECTED TO DIFFERENT SALINITY LEVELS
    CHEN, JC
    LIN, JL
    [J]. AQUACULTURE, 1994, 125 (1-2) : 167 - 174
  • [6] Ontogeny of osmoregulatory structures and functions in the green crab Carcinus maenas (Crustacea, Decapoda)
    Cieluch, U
    Anger, K
    Aujoulat, F
    Buchholz, F
    Charmantier-Daures, M
    Charmantier, G
    [J]. JOURNAL OF EXPERIMENTAL BIOLOGY, 2004, 207 (02) : 325 - 336
  • [7] PARTIAL-PURIFICATION AND PROPERTIES OF CARMINOMYCIN 4-O-METHYLTRANSFERASE FROM STREPTOMYCES SP STRAIN C5
    CONNORS, NC
    STROHL, WR
    [J]. JOURNAL OF GENERAL MICROBIOLOGY, 1993, 139 : 1353 - 1362
  • [8] Morphological and biochemical changes in the muscle of the marine shrimp Litopenaeus vannamei during the molt cycle
    de Oliveira Cesar, Jose Renato
    Zhao, Baoping
    Malecha, Spencer
    Ako, Harry
    Yang, Jinzeng
    [J]. AQUACULTURE, 2006, 261 (02) : 688 - 694
  • [9] Comparative immunohistochemistry and cellular distribution of farnesoic acid O-methyltransferase in the shrimp and the crayfish
    Gunawardene, YINS
    Bendena, WG
    Tobe, SS
    Chan, SM
    [J]. PEPTIDES, 2003, 24 (10) : 1591 - 1597
  • [10] Function and cellular localization of farnesoic acid O-methyltransferase (FAMeT) in the shrimp, Metapenaeus ensis
    Gunawardene, YINS
    Tobe, SS
    Bendena, WG
    Chow, BKC
    Yagi, KJ
    Chan, SM
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (14): : 3587 - 3595