Isolation of SFRS3 gene and its differential expression during metamorphosis involving eye migration of Japanese flounder Paralichthys olivaceus

被引:27
作者
Bao, BL [1 ]
Yang, GM
Liu, ZJ
Li, SH
Wang, ZL
Ren, DM
机构
[1] Fudan Univ, State Key Lab Genet Engn, Inst Genet, Shanghai 200433, Peoples R China
[2] Shanghai Fisheries Univ, Coll Aquat Life Sci & Technol, Shanghai 200090, Peoples R China
[3] Auburn Univ, Dept Fisheries & Allied Aquacultures, Auburn, AL 36949 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2005年 / 1725卷 / 01期
关键词
SFRS3; fish; flounder; metamorphosis; eye; development;
D O I
10.1016/j.bbagen.2005.04.032
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
Both eyes of flatfishes are located on one side of the body due to asymmetrical eye migration. The molecular mechanisms underlying such asymmetry is poorly understood. As an initial step, we have adopted suppression subtractive hybridization for the identification of upregulated genes during metamorphosis involving eye migration in Japanese flounder, Paralichthys olicaceus. One of the upregulated genes was identified as the splicing factor arginine/serine rich-3 (SFRS3). Sequence analysis of SFRS3 revealed that it encodes a protein of 168 amino acids containing the typical eukaryotic RNA recognition motif (RRM) and an arginine/serine-rich region. The overall amino acid sequences of the Japanese flounder SFRS3 was highly conserved with that of other organisms. The expression of flounder SFRS3 gene increased sharply from the beginning of metamorphosis and reached a high level of expression at stage H of metamorphosis 43 days after hatching. The SFRS3 gene upregulation was mainly limited to the head region, particularly in the rapidly proliferative tissues, the lateral ethmoid and "skin thickness" on blind side, which are thought as two proliferative tissues to push the eye movement. In spite of the upregulated expression of SFRS3 during metamorphosis, its role in metamorphosis involving eye migration requires further studies. (c) 2005 Elsevier B.V. All rights reseved.
引用
收藏
页码:64 / 70
页数:7
相关论文
共 33 条
[1]  
Bisgrove BW, 2000, DEVELOPMENT, V127, P3567
[2]   EYE MIGRATION AND CRANIAL DEVELOPMENT DURING FLATFISH METAMORPHOSIS - A REAPPRAISAL (TELEOSTEI, PLEURONECTIFORMES) [J].
BREWSTER, B .
JOURNAL OF FISH BIOLOGY, 1987, 31 (06) :805-833
[3]  
Burdine RD, 2000, GENE DEV, V14, P763
[4]  
Campione M, 1999, DEVELOPMENT, V126, P1225
[5]   Mechanisms of left-right determination in vertebrates [J].
Capdevila, J ;
Vogan, KJ ;
Tabin, CJ ;
Belmonte, JCI .
CELL, 2000, 101 (01) :9-21
[6]   CHARACTERIZATION AND CLONING OF THE HUMAN SPLICING FACTOR 9G8 - A NOVEL 35 KDA FACTOR OF THE SERINE/ARGININE PROTEIN FAMILY [J].
CAVALOC, Y ;
POPIELARZ, M ;
FUCHS, JP ;
GATTONI, R ;
STEVENIN, J .
EMBO JOURNAL, 1994, 13 (11) :2639-2649
[7]   Suppression subtractive hybridization: A method for generating differentially regulated or tissue-specific cDNA probes and libraries [J].
Diatchenko, L ;
Lau, YFC ;
Campbell, AP ;
Chenchik, A ;
Moqadam, F ;
Huang, B ;
Lukyanov, S ;
Lukyanov, K ;
Gurskaya, N ;
Sverdlov, ED ;
Siebert, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :6025-6030
[8]   GENERAL SPLICING FACTORS SF2 AND SC35 HAVE EQUIVALENT ACTIVITIES INVITRO, AND BOTH AFFECT ALTERNATIVE 5' AND 3' SPLICE SITE SELECTION [J].
FU, XD ;
MAYEDA, A ;
MANIATIS, T ;
KRAINER, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (23) :11224-11228
[9]   A PROTEIN FACTOR, ASF, CONTROLS CELL-SPECIFIC ALTERNATIVE SPLICING OF SV40 EARLY PRE-MESSENGER-RNA INVITRO [J].
GE, H ;
MANLEY, JL .
CELL, 1990, 62 (01) :25-34
[10]   Links in the left/right axial pathway [J].
Harvey, RP .
CELL, 1998, 94 (03) :273-276