Cloning and characterization of a novel serine/threonine protein phosphatase type 5 from Trypanosoma brucei

被引:37
作者
Chaudhuri, M [1 ]
机构
[1] Meharry Med Coll, Dept Microbiol, Nashville, TN 37208 USA
关键词
Trypanosoma brucei; serine/threonine protein phosphatase type 5; TPR motifs; arachidonic acid;
D O I
10.1016/S0378-1119(01)00367-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Reversible protein phosphorylation is essential for the regulation of numerous cellular functions and differentiation. The haemo-flagellated parasitic protozoan Trypanosoma brucei, the causative agent for Africa trypanosomiasis undergoes various stages of cellular differentiation during its digenetic life cycle. A complete cDNA of a unique serine/threonine phosphatase: type five (TbPP5) was cloned and characterized from T. brucei. TbPPS contains an open reading frame of 1416 bp that encodes a protein of about 53 kDa and exists as a single copy gene in the T. brucei genome. The deduced amino acid sequence showed 45-48% overall identity and 60-65% similarity with protein phosphatase 5 's (PP5) from different species. Analysis of the primary sequence revealed that TbPPS contains three TPR motifs at the N-terminal region (amino acid residues 7-107) while the phosphatase catalytic domain occurs in the C-terminal region (amino acid residues 210-410). A TbPPS cDNA hybridized with a transcript of 2.5 kb which is present at similar levels in the procyclic and the bloodstream forms. However, the level of expression of the TbPPS protein (52 kDa) detected by an antibody developed against a recombinant protein produced in E. coli was about 2-fold higher in the procyclic than the bloodstream form. The TbPP5 transcript level gradually decreased in cells grown in the logarithmic phase to the stationary phase in culture. Moreover, 18 h serum starvation of the procyclic forms decreased the level of the specific transcript about 3-fold suggesting that this: protein may play a role during the active growth phase of the organism. The recombinant protein showed phosphatase activity which was stimulated about 2.6-fold by arachidonic acid with half-maximal activity at 75 muM Indirect immuno-fluoresence of permeabilized cells revealed that the protein is localized in the cytosol and the nucleus This is the first report for the identification of a type 5 serine/threonine protein phosphatase in an ancient eukaryote such as T. brucei. (C) 2001 Elsevier Science B.V. All rights reserved.
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页码:1 / 13
页数:13
相关论文
共 41 条
[1]   ISOLATION OF A MITOTIC-LIKE CYCLIN HOMOLOG FROM THE PROTOZOAN TRYPANOSOMA-BRUCEI [J].
AFFRANCHINO, JL ;
GONZALEZ, SA ;
PAYS, E .
GENE, 1993, 132 (01) :75-82
[2]  
Alschul S F, 1990, J Mol Biol, V215, P403
[3]   Purification, cloning, and characterization of an acidic ectoprotein phosphatase differentially expressed in the infectious bloodstream form of Trypanosoma brucei [J].
Bakalara, N ;
Santarelli, X ;
Davis, C ;
Baltz, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :8863-8871
[4]   Molecular mechanisms of the protein serine threonine phosphatases [J].
Barford, D .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (11) :407-412
[5]   Drosophila protein phosphatase 5 is encoded by a single gene that is most highly expressed during embryonic development [J].
Brown, L ;
Borthwick, EB ;
Cohen, PTW .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2000, 1492 (2-3) :470-476
[6]   HIGH-EFFICIENCY CLONAL GROWTH OF BLOOD-STREAM-FORM AND INSECT-FORM TRYPANOSOMA-BRUCEI ON AGAROSE PLATES [J].
CARRUTHERS, VB ;
CROSS, GAM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (18) :8818-8821
[7]   A NOVEL HUMAN PROTEIN SERINE/THREONINE PHOSPHATASE, WHICH POSSESSES 4 TETRATRICOPEPTIDE REPEAT MOTIFS AND LOCALIZES TO THE NUCLEUS [J].
CHEN, MX ;
MCPARTLIN, AE ;
BROWN, L ;
CHEN, YH ;
BARKER, HM ;
COHEN, PTW .
EMBO JOURNAL, 1994, 13 (18) :4278-4290
[8]   Activation of protein phosphatase 5 by limited proteolysis or the binding of polyunsaturated fatty acids to the TPR domain [J].
Chen, MX ;
Cohen, PTW .
FEBS LETTERS, 1997, 400 (01) :136-140
[9]   TARGETING OF A DISTINCTIVE PROTEIN-SERINE PHOSPHATASE TO THE PROTEIN KINASE-LIKE DOMAIN OF THE ATRIAL-NATRIURETIC-PEPTIDE RECEPTOR [J].
CHINKERS, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) :11075-11079
[10]   DEVELOPMENTAL REGULATION OF NUCLEAR GENE-EXPRESSION IN TRYPANOSOMA-BRUCEI [J].
CLAYTON, C .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, 1992, 43 :37-66