Literature DB >> 7494636

Two types of aminoacyl-tRNA synthetases could be originally encoded by complementary strands of the same nucleic acid.

S N Rodin1, S Ohno.   

Abstract

The lack of even a marginal similarity between the two aminoacyl-tRNA synthetase (aaRS) classes suggests their independent origins (Eriani et al., 1990; Nagel and Doolittle, 1991). Yet, this independence is a puzzle inconsistent with the common origin of transfer RNAs, the coevolutionary theory of the genetic code (Wong, 1975, 1981) and other associated data and ideas. We present here the results of antiparallel 'class I versus class II' comparisons of aaRSs within their signature sequences. The two main HIGH- and KMSKS-containing motifs of class I appeared to be complementary to the class II motifs 2 and 1, respectively. The above sequence complementarity along with the mirror-image between crystal structures of complexes formed by the opposite aaRSs and their cognate tRNAs (Ruff et al., 1991), and the generally mirror ('head-to-tail') mapping of the basic functional sites in the sequences of aaRSs from the opposite two classes led us to conclude that these two synthetases emerged synchronously as complementary strands of the same primordial nucleic acid. This conclusion, combined with the hypothesis of tRNA concerted origin (Rodin et al., 1993a,b), may explain many intriguing features of aaRSs and favor the elucidation of the origin of the genetic code.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7494636     DOI: 10.1007/bf01582025

Source DB:  PubMed          Journal:  Orig Life Evol Biosph        ISSN: 0169-6149            Impact factor:   1.950


  42 in total

1.  Evolution of metabolic pathways by chance assembly of enzyme proteins generated from sense and antisense strands of pre-existing genes.

Authors:  S Fukuchi; J Otsuka
Journal:  J Theor Biol       Date:  1992-10-07       Impact factor: 2.691

2.  VOSTORG: a package of microcomputer programs for sequence analysis and construction of phylogenetic trees.

Authors:  A A Zharkikh; P S Morosov; T L Sitnikova; J S Krushkal
Journal:  Gene       Date:  1991-05-30       Impact factor: 3.688

3.  Speculations on the early course of evolution.

Authors:  J E Darnell; W F Doolittle
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

4.  Transfer RNAs with complementary anticodons: could they reflect early evolution of discriminative genetic code adaptors?

Authors:  S Rodin; S Ohno; A Rodin
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-15       Impact factor: 11.205

5.  Doublet frequencies in evolutionary distinct groups.

Authors:  R Nussinov
Journal:  Nucleic Acids Res       Date:  1984-02-10       Impact factor: 16.971

6.  Structural similarities in glutaminyl- and methionyl-tRNA synthetases suggest a common overall orientation of tRNA binding.

Authors:  J J Perona; M A Rould; T A Steitz; J L Risler; C Zelwer; S Brunie
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-01       Impact factor: 11.205

7.  Similarity between the corticotropin (ACTH) receptor and a peptide encoded by an RNA that is complementary to ACTH mRNA.

Authors:  K L Bost; E M Smith; J E Blalock
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

8.  Is there a relationship between DNA sequences encoding peptide ligands and their receptors?

Authors:  A Goldstein; D L Brutlag
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

9.  Region of a conserved sequence motif in a class II tRNA synthetase needed for transfer of an activated amino acid to an RNA substrate.

Authors:  J P Shi; K Musier-Forsyth; P Schimmel
Journal:  Biochemistry       Date:  1994-05-03       Impact factor: 3.162

10.  Universal rule for coding sequence construction: TA/CG deficiency-TG/CT excess.

Authors:  S Ohno
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

View more
  46 in total

1.  An asymmetric underlying rule in the assignment of codons: possible clue to a quick early evolution of the genetic code via successive binary choices.

Authors:  Marc Delarue
Journal:  RNA       Date:  2006-12-12       Impact factor: 4.942

2.  Evolution of the genetic code by incorporation of amino acids that improved or changed protein function.

Authors:  Brian R Francis
Journal:  J Mol Evol       Date:  2013-06-07       Impact factor: 2.395

Review 3.  Development of tRNA synthetases and connection to genetic code and disease.

Authors:  Paul Schimmel
Journal:  Protein Sci       Date:  2008-09-02       Impact factor: 6.725

4.  On primordial sense-antisense coding.

Authors:  Andrei S Rodin; Sergei N Rodin; Charles W Carter
Journal:  J Mol Evol       Date:  2009-12-03       Impact factor: 2.395

5.  Four primordial modes of tRNA-synthetase recognition, determined by the (G,C) operational code.

Authors:  S N Rodin; S Ohno
Journal:  Proc Natl Acad Sci U S A       Date:  1997-05-13       Impact factor: 11.205

6.  Functional Class I and II Amino Acid-activating Enzymes Can Be Coded by Opposite Strands of the Same Gene.

Authors:  Luis Martinez-Rodriguez; Ozgün Erdogan; Mariel Jimenez-Rodriguez; Katiria Gonzalez-Rivera; Tishan Williams; Li Li; Violetta Weinreb; Martha Collier; Srinivas Niranj Chandrasekaran; Xavier Ambroggio; Brian Kuhlman; Charles W Carter
Journal:  J Biol Chem       Date:  2015-06-18       Impact factor: 5.157

Review 7.  Urzymology: experimental access to a key transition in the appearance of enzymes.

Authors:  Charles W Carter
Journal:  J Biol Chem       Date:  2014-09-10       Impact factor: 5.157

8.  The presence of codon-anticodon pairs in the acceptor stem of tRNAs.

Authors:  S Rodin; A Rodin; S Ohno
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-14       Impact factor: 11.205

9.  One ancestor for two codes viewed from the perspective of two complementary modes of tRNA aminoacylation.

Authors:  Andrei S Rodin; Eörs Szathmáry; Sergei N Rodin
Journal:  Biol Direct       Date:  2009-01-27       Impact factor: 4.540

10.  Undetected antisense tRNAs in mitochondrial genomes?

Authors:  Hervé Seligmann
Journal:  Biol Direct       Date:  2010-06-16       Impact factor: 4.540

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.