Cloning and characterization of the 14-3-3 protein gene from the halotolerant alga Dunaliella salina

被引:9
作者
Wang, Tianyun [1 ,2 ]
Xue, Lexun [1 ]
Ji, Xiang [1 ]
Li, Jie [1 ]
Wang, Yafeng [1 ]
Feng, Yingcai [1 ]
机构
[1] Zhengzhou Univ, Cell Biol Lab, Zhengzhou 450052, Henan, Peoples R China
[2] Xinxiang Med Univ, Dept Biochem & Mol Biol, Xinxiang 453003, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
14-3-3; Protein; Dunaliella salina; Molecular evolution; AMINO-ACID-SEQUENCE; CHLAMYDOMONAS-REINHARDTII; NUCLEOTIDE-SEQUENCE; SIGNALING PROTEINS; 14-3-3-PROTEINS; EXPRESSION; FAMILY; ORGANIZATION; CDNA;
D O I
10.1007/s11033-007-9168-1
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
Previous studies have demonstrated that 14-3-3 proteins exist in all the eukaryotic organisms studied; however, studies on the 14-3-3 proteins have not been involved in the halotolerant, unicellular green alga Dunaliella salina so far. In the present study, a cDNA encoding 14-3-3 protein of D. salina was cloned and sequenced by PCR and rapid amplification of cDNA end (RACE) technique based on homologous sequences of the 14-3-3 proteins found in other organisms. The cloned cDNA of 1485 bp in length had a 29.2 kDa of molecular weight and contained a 774 bp of open reading frame encoding a polypeptide of 258 amino acids. Like the other 14-3-3 proteins, the deduced amino acid sequences of the D. salina 14-3-3 protein also contained two putative phosphorylation sites within the N-terminal region (positions 62 and 67). Furthermore, an EF hand motif characteristic for Ca2+-binding sites was located within the C-terminal part of this polypeptide (positions 208-219). Analysis of bioinformatics revealed that the 14-3-3 protein of D. salina shared homology with that of other organisms. Real-time quantitative PCR demonstrated that expression of the 14-3-3 protein gene is cell cycle-dependent.
引用
收藏
页码:207 / 214
页数:8
相关论文
共 22 条
[1]   14-3-3-ALPHA AND 14-3-3-DELTA ARE THE PHOSPHORYLATED FORMS OF RAF-ACTIVATING 14-3-3-BETA AND 14-3-3-ZETA - IN-VIVO STOICHIOMETRIC PHOSPHORYLATION IN BRAIN AT A SER-PRO-GLU-LYS MOTIF [J].
AITKEN, A ;
HOWELL, S ;
JONES, D ;
MADRAZO, J ;
PATEL, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :5706-5709
[2]   14-3-3 proteins: A historic overview [J].
Aitken, Alastair .
SEMINARS IN CANCER BIOLOGY, 2006, 16 (03) :162-172
[3]  
AITKEN DW, 1992, NUCLEUS-CAMBRIDGE, V14, P3
[4]   NPS@:: Network Protein Sequence Analysis [J].
Combet, C ;
Blanchet, C ;
Geourjon, C ;
Deléage, G .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :147-150
[5]   Molecular organization and tissue-specific expression of an Arabidopsis 14-3-3 gene [J].
Daugherty, CJ ;
Rooney, MF ;
Miller, PW ;
Ferl, RJ .
PLANT CELL, 1996, 8 (08) :1239-1248
[6]   WIDESPREAD DISTRIBUTION OF THE 14-3-3 PROTEIN IN VERTEBRATE BRAINS AND BOVINE-TISSUES - CORRELATION WITH THE DISTRIBUTIONS OF CALCIUM-DEPENDENT PROTEIN-KINASES [J].
ICHIMURA, T ;
SUGANO, H ;
KUWANO, R ;
SUNAYA, T ;
OKUYAMA, T ;
ISOBE, T .
JOURNAL OF NEUROCHEMISTRY, 1991, 56 (04) :1449-1451
[7]   A CHLAMYDOMONAS HOMOLOG TO THE 14-3-3-PROTEINS - CDNA AND DEDUCED AMINO-ACID-SEQUENCE [J].
LIEBICH, I ;
VOIGT, J .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1995, 1263 (01) :79-85
[8]  
Moore B.W., 1967, Physiological and Biochemical Aspects of Nervous Integratin, P343
[9]   14-3-3 - MODULATORS OF SIGNALING PROTEINS [J].
MORRISON, D .
SCIENCE, 1994, 266 (5182) :56-57
[10]   Five new 14-3-3 isoforms from Nicotiana tabacum L.: Implications for the phylogeny of plant 14-3-3 proteins [J].
Piotrowski M. ;
Oecking C. .
Planta, 1997, 204 (1) :127-130