Sequence and phylogenetic analyses of the twin-arginine targeting (Tat) protein export system

被引:142
作者
Yen, MR
Tseng, YH
Nguyen, EH
Wu, LF
Saier, MH [1 ]
机构
[1] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
[2] Natl Chung Hsing Univ, Inst Mol Biol, Taichung 402, Taiwan
[3] Inst Biol Struct & Microbiol, UPR9043 CNRS, Chim Bacterienne Lab, F-13402 Marseille 20, France
关键词
twin-arginine targeting; protein secretion; evolution; phylogeny;
D O I
10.1007/s00203-002-0408-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Twin-arginine targeting (Tat) protein secretion systems consist of two protein types, members of the TatA and TatC families. Homologues of these proteins are found in many archaea, bacteria, chloroplasts and mitochondria. Every prokaryotic organism with a fully sequenced genome exhibits either neither family member, or between one and three paralogues of these two family members. The Arabidopsis thaliana genome encodes three of each. Although many mitochondrially encoded TatC homologues have been identified, corresponding TatA homologues have not been found in this organelle. Phylogenetic analyses reveal that most prokaryotic Tat systems consist of one TatC homologue and two sequence-divergent TatA homologues (TatA and TatB). When only one TatA homologue is present, TatB is missing, and when three TatA homologues are present, the third one arose by duplication of TatA, not TatB. Further, homologues most resembling TatB are more sequence-divergent than those more closely resembling TatA. In contrast to the TatA family, the TatC family shows phylogenetic clustering in strict accordance with organismal type. These results are discussed in terms of their probable structural, functional and evolutionary significance.
引用
收藏
页码:441 / 450
页数:10
相关论文
共 42 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Export of Thermus thermophilus alkaline phosphatase via the twin-arginine translocation pathway in Escherichia coli [J].
Angelini, S ;
Moreno, R ;
Gouffi, K ;
Santini, CL ;
Yamagishi, A ;
Berenguer, J ;
Wu, LF .
FEBS LETTERS, 2001, 506 (02) :103-107
[3]   The Tat protein export pathway [J].
Berks, BC ;
Sargent, F ;
Palmer, T .
MOLECULAR MICROBIOLOGY, 2000, 35 (02) :260-274
[4]   A novel protein transport system involved in the biogenesis of bacterial electron transfer chains [J].
Berks, BC ;
Sargent, F ;
De Leeuw, E ;
Hinsley, AP ;
Stanley, NR ;
Jack, RL ;
Buchanan, G ;
Palmer, T .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2000, 1459 (2-3) :325-330
[5]   A common export pathway for proteins binding complex redox cofactors? [J].
Berks, BC .
MOLECULAR MICROBIOLOGY, 1996, 22 (03) :393-404
[6]   Ralstonia eutropha TF93 is blocked in tat-mediated protein export [J].
Bernhard, M ;
Friedrich, B ;
Siddiqui, RA .
JOURNAL OF BACTERIOLOGY, 2000, 182 (03) :581-588
[7]   Specificity of signal peptide recognition in Tat-dependent bacterial protein translocation [J].
Blaudeck, N ;
Sprenger, GA ;
Freudl, R ;
Wiegert, T .
JOURNAL OF BACTERIOLOGY, 2001, 183 (02) :604-610
[8]   An essential component of a novel bacterial protein export system with homologues in plastids and mitochondria [J].
Bogsch, EG ;
Sargent, F ;
Stanley, NR ;
Berks, BC ;
Robinson, C ;
Palmer, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (29) :18003-18006
[9]   TatB and TatC form a functional and structural unit of the twin-arginine translocase from Escherichia coli [J].
Bolhuis, A ;
Mathers, JE ;
Thomas, JD ;
Barrett, CML ;
Robinson, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (23) :20213-20219
[10]   Potential receptor function of three homologous components, TatA, TatB and TatE, of the twin-arginine signal sequence-dependent metalloenzyme translocation pathway in Escherichia coli [J].
Chanal, A ;
Santini, CL ;
Wu, LF .
MOLECULAR MICROBIOLOGY, 1998, 30 (03) :674-676