Comparative genomics and evolution of proteins involved in RNA metabolism

被引:414
作者
Anantharaman, V [1 ]
Koonin, EV [1 ]
Aravind, L [1 ]
机构
[1] Natl Lib Med, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA
关键词
D O I
10.1093/nar/30.7.1427
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
RNA metabolism, broadly defined as the compendium of all processes that involve RNA, including transcription, processing and modification of transcripts, translation, RNA degradation and its regulation, is the central and most evolutionarily conserved part of cell physiology. A comprehensive, genome-wide census of all enzymatic and non-enzymatic protein domains involved in RNA metabolism was conducted by using sequence profile analysis and structural comparisons. Proteins related to RNA metabolism comprise from 3 to 11% of the complete protein repertoire in bacteria, archaea and eukaryotes, with the greatest fraction seen in parasitic bacteria with small genomes. Approximately one-half of protein domains involved in RNA metabolism are present in most, if not all, species from all three primary kingdoms and are traceable to the last universal common ancestor (LUCA). The principal features of LUCA's RNA metabolism system were reconstructed by parsimony-based evolutionary analysis of all relevant groups of orthologous proteins. This reconstruction shows that LUCA possessed not only the basal translation system, but also the principal forms of RNA modification, such as methylation, pseudouridylation and thiouridylation, as well as simple mechanisms for polyadenylation and RNA degradation. Some of these ancient domains form paralogous groups whose evolution can be traced back in time beyond LUCA, towards low-specificity proteins, which probably functioned as cofactors for ribozymes within the RNA world framework. The main lineage-specific innovations of RNA metabolism systems were identified. The most notable phase of innovation in RNA metabolism coincides with the advent of eukaryotes and was brought about by the merge of the archaeal and bacterial systems via mitochondrial endosymbiosis, but also involved emergence of several new, eukaryote-specific RNA-binding domains. Subsequent, vast expansions of these domains mark the origin of alternative splicing in animals and probably in plants. In addition to the reconstruction of the evolutionary history of RNA metabolism, this analysis produced numerous functional predictions, e.g. of previously undetected enzymes of RNA modification.
引用
收藏
页码:1427 / 1464
页数:38
相关论文
共 285 条
[51]  
CAVALIERSMITH T, 1991, TRENDS GENET, V7, P145, DOI 10.1016/0168-9525(91)90377-3
[52]   Domains in gene silencing and cell differentiation proteins: the novel PAZ domain and redefinition of the Piwi domain [J].
Cerutti, L ;
Mian, N ;
Bateman, A .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (10) :481-482
[53]   Essential yeast protein with unexpected similarity to subunits of mammalian cleavage and polyadenylation specificity factor (CPSF) [J].
Chanfreau, G ;
Noble, SM ;
Guthrie, C .
SCIENCE, 1996, 274 (5292) :1511-1514
[54]   Crystal structure of ERA: A GTPase-dependent cell cycle regulator containing an RNA binding motif [J].
Chen, X ;
Court, DL ;
Ji, XH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8396-8401
[55]  
Chen XG, 2000, GENE DEV, V14, P777
[56]   PIN domains in nonsense-mediated mRNA decay and RNAi [J].
Clissold, PM ;
Ponting, CP .
CURRENT BIOLOGY, 2000, 10 (24) :R888-R890
[57]   Reconstitution of a minimal RNA degradosome demonstrates functional coordination between a 3′ exonuclease and a DEAD-box RNA helicase [J].
Coburn, GA ;
Miao, X ;
Briant, DJ ;
Mackie, GA .
GENES & DEVELOPMENT, 1999, 13 (19) :2594-2603
[58]   Posttranscriptional gene silencing in Neurospora by a RecQ DNA helicase [J].
Cogoni, C ;
Macino, G .
SCIENCE, 1999, 286 (5448) :2342-2344
[59]   Gene silencing in Neurospora crassa requires a protein homologous to RNA-dependent RNA polymerase [J].
Cogoni, C ;
Macino, G .
NATURE, 1999, 399 (6732) :166-169
[60]   Post-transcriptional gene silencing across kingdoms [J].
Cogoni, C ;
Macino, G .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2000, 10 (06) :638-643