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
[21]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[22]   TETRATRICO PEPTIDE REPEAT INTERACTIONS - TO TPR OR NOT TO TPR [J].
LAMB, JR ;
TUGENDREICH, S ;
HIETER, P .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (07) :257-259
[23]   SEPARATION OF TRYPANOSOMES FROM BLOOD OF INFECTED RATS AND MICE BY ANION-EXCHANGERS [J].
LANHAM, SM .
NATURE, 1968, 218 (5148) :1273-&
[24]  
LIE S, 1995, BIOCHEM BIOPH RES CO, V212, P793
[25]  
MAYERS EW, 1998, COMPUT APPL BIOSCI, V4, P11
[26]   A FAMILY OF TRYPANOSOME CDC2-RELATED PROTEIN-KINASES [J].
MOTTRAM, JC ;
SMITH, G .
GENE, 1995, 162 (01) :147-152
[27]   Cyclic AMP signaling in trypanosomatids [J].
Naula, C ;
Seebeck, T .
PARASITOLOGY TODAY, 2000, 16 (01) :35-38
[28]   TRANSSPLICING - AN UPDATE [J].
NILSEN, TW .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 73 (1-2) :1-6
[29]   The serine/threonine phosphatase PP5 interacts with CDC16 and CDC27, two tetratricopeptide repeat-containing subunits of the anaphase-promoting complex [J].
Ollendorf, V ;
Donoghue, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32011-32018
[30]   Pathways involved in environmental sensing in trypanosomatids [J].
Parsons, M ;
Ruben, L .
PARASITOLOGY TODAY, 2000, 16 (02) :56-62