The evolutionary history of Cys-tRNACys formation

被引:61
作者
O'Donoghue, P
Sethi, A
Woese, CR
Luthey-Schulten, ZA
机构
[1] Univ Illinois, Dept Microbiol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
关键词
aminoacyl-tRNA synthetase; cysteine; methanogenic archaea; O-phosphoserine; structure and sequence-based phylogeny;
D O I
10.1073/pnas.0509617102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The recent discovery of an alternate pathway for indirectly charging tRNA(cYs) has stimulated a re-examination of the evolutionary history of Cys-tRNA(cys) formation. In the first step of the pathway, O-phosphoseryl-tRNA synthetase charges tRNA(cy5) with O-phosphoserine (Sep), a precursor of the cognate amino acid. In the following step, Sep-tRNA:Cys-tRNA synthase (SepCysS) converts Sep to Cys in a tRNA-dependent reaction. The existence of such a pathway raises several evolutionary questions, including whether the indirect pathway is a recent evolutionary invention, as might be implied from its localization to the Euryarchaea, or, as evidence presented here indicates, whether this pathway is more ancient, perhaps already in existence at the time of the last universal common ancestral state. A comparative phylogenetic approach is used, combining evolutionary information from protein sequences and structures, that takes both the signature of horizontal gene transfer and the recurrence of the full canonical phylogenetic pattern into account, to document the complete evolutionary history of cysteine coding and understand the nature of this process in the last universal common ancestral state. Resulting from the historical study of tRNA(cys) aminoacylation and the integrative perspective of sequence, structure, and function are 3D models of 0-phosphoseryl-tRNA synthetase and SepCysS, which provide experimentally testable predictions regarding the identity and function of key active-site residues in these proteins. The model of SepCysS is used to suggest a sulfhydrylation reaction mechanism, which is predicted to occur at the interface of a SepCysS dimer.
引用
收藏
页码:19003 / 19008
页数:6
相关论文
共 51 条
[1]  
ADACHI J, 1996, COMPUT SCI MONOGR, V28, P1
[2]   SCOP database in 2004: refinements integrate structure and sequence family data [J].
Andreeva, A ;
Howorth, D ;
Brenner, SE ;
Hubbard, TJP ;
Chothia, C ;
Murzin, AG .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D226-D229
[3]   The universal protein resource (UniProt) [J].
Bairoch, A ;
Apweiler, R ;
Wu, CH ;
Barker, WC ;
Boeckmann, B ;
Ferro, S ;
Gasteiger, E ;
Huang, HZ ;
Lopez, R ;
Magrane, M ;
Martin, MJ ;
Natale, DA ;
O'Donovan, C ;
Redaschi, N ;
Yeh, LSL .
NUCLEIC ACIDS RESEARCH, 2005, 33 :D154-D159
[4]  
Bapteste Eric, 2005, Archaea, V1, P353, DOI 10.1155/2005/859728
[5]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[6]   An emerging phylogenetic core of Archaea: phylogenies of transcription and translation machineries converge following addition of new genome sequences [J].
Brochier, C ;
Forterre, P ;
Gribaldo, S .
BMC EVOLUTIONARY BIOLOGY, 2005, 5 (1)
[7]   Archaeal phylogeny based on proteins of the transcription and translation machineries:: tackling the Methanopyrus kandleri paradox -: art. no. R17 [J].
Brochier, C ;
Forterre, P ;
Gribaldo, S .
GENOME BIOLOGY, 2004, 5 (03)
[8]   Complete genome sequence of the methanogenic archaeon, Methanococcus jannaschii [J].
Bult, CJ ;
White, O ;
Olsen, GJ ;
Zhou, LX ;
Fleischmann, RD ;
Sutton, GG ;
Blake, JA ;
FitzGerald, LM ;
Clayton, RA ;
Gocayne, JD ;
Kerlavage, AR ;
Dougherty, BA ;
Tomb, JF ;
Adams, MD ;
Reich, CI ;
Overbeek, R ;
Kirkness, EF ;
Weinstock, KG ;
Merrick, JM ;
Glodek, A ;
Scott, JL ;
Geoghagen, NSM ;
Weidman, JF ;
Fuhrmann, JL ;
Nguyen, D ;
Utterback, TR ;
Kelley, JM ;
Peterson, JD ;
Sadow, PW ;
Hanna, MC ;
Cotton, MD ;
Roberts, KM ;
Hurst, MA ;
Kaine, BP ;
Borodovsky, M ;
Klenk, HP ;
Fraser, CM ;
Smith, HO ;
Woese, CR ;
Venter, JC .
SCIENCE, 1996, 273 (5278) :1058-1073
[9]   Reconstitution of a new cysteine biosynthetic pathway in Mycobacterium tuberculosis [J].
Burns, KE ;
Baumgart, S ;
Dorrestein, PC ;
Zhai, HL ;
McLafferty, FW ;
Begley, TP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (33) :11602-11603
[10]   The ASTRAL Compendium in 2004 [J].
Chandonia, JM ;
Hon, G ;
Walker, NS ;
Lo Conte, L ;
Koehl, P ;
Levitt, M ;
Brenner, SE .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D189-D192