Serveur d'exploration MERS

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

A Model of Proto-Anti-Codon RNA Enzymes Requiring l -Amino Acid Homochirality

Identifieur interne : 002623 ( Main/Merge ); précédent : 002622; suivant : 002624

A Model of Proto-Anti-Codon RNA Enzymes Requiring l -Amino Acid Homochirality

Auteurs : Albert Erives [États-Unis]

Source :

RBID : ISTEX:40AC08D061A237AD2B4F8868FD55DA8B82A692AE

English descriptors

Abstract

Abstract: All living organisms encode the 20 natural amino acid units of polypeptides using a universal scheme of triplet nucleotide “codons”. Disparate features of this codon scheme are potentially informative of early molecular evolution: (i) the absence of any codons for d-amino acids; (ii) the odd combination of alternate codon patterns for some amino acids; (iii) the confinement of synonymous positions to a codon’s third nucleotide; (iv) the use of 20 specific amino acids rather than a number closer to the full coding potential of 64; and (v) the evolutionary relationship of patterns in stop codons to amino acid codons. Here I propose a model for an ancestral proto-anti-codon RNA (pacRNA) auto-aminoacylation system and show that pacRNAs would naturally manifest features of the codon table. I show that pacRNAs could implement all the steps for auto-aminoacylation: amino acid coordination, intermediate activation of the amino acid by the 5′-end of the pacRNA, and 3′-aminoacylation of the pacRNA. The anti-codon cradles of pacRNAs would have been able to recognize and coordinate only a small number of l-amino acids via hydrogen bonding. A need for proper spatial coordination would have limited the number of chargeable amino acids for all anti-codon sequences, in addition to making some anti-codon sequences unsuitable. Thus, the pacRNA model implies that the idiosyncrasies of the anti-codon table and l-amino acid homochirality co-evolved during a single evolutionary period. These results further imply that early life consisted of an aminoacylated RNA world with a richer enzymatic potential than ribonucleotides alone.

Url:
DOI: 10.1007/s00239-011-9453-4

Links toward previous steps (curation, corpus...)


Links to Exploration step

ISTEX:40AC08D061A237AD2B4F8868FD55DA8B82A692AE

Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">A Model of Proto-Anti-Codon RNA Enzymes Requiring l -Amino Acid Homochirality</title>
<author>
<name sortKey="Erives, Albert" sort="Erives, Albert" uniqKey="Erives A" first="Albert" last="Erives">Albert Erives</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:40AC08D061A237AD2B4F8868FD55DA8B82A692AE</idno>
<date when="2011" year="2011">2011</date>
<idno type="doi">10.1007/s00239-011-9453-4</idno>
<idno type="url">https://api.istex.fr/ark:/67375/VQC-N6QL1RQH-F/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000A33</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000A33</idno>
<idno type="wicri:Area/Istex/Curation">000A33</idno>
<idno type="wicri:Area/Istex/Checkpoint">000527</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000527</idno>
<idno type="wicri:doubleKey">0022-2844:2011:Erives A:a:model:of</idno>
<idno type="wicri:Area/Main/Merge">002623</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">A Model of Proto-Anti-Codon RNA Enzymes Requiring l -Amino Acid Homochirality</title>
<author>
<name sortKey="Erives, Albert" sort="Erives, Albert" uniqKey="Erives A" first="Albert" last="Erives">Albert Erives</name>
<affiliation wicri:level="1">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biological Sciences, Dartmouth College, 03755, Hanover, NH</wicri:regionArea>
<wicri:noRegion>NH</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<country wicri:rule="url">États-Unis</country>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Journal of Molecular Evolution</title>
<title level="j" type="abbrev">J Mol Evol</title>
<idno type="ISSN">0022-2844</idno>
<idno type="eISSN">1432-1432</idno>
<imprint>
<publisher>Springer-Verlag</publisher>
<pubPlace>New York</pubPlace>
<date type="published" when="2011-08-01">2011-08-01</date>
<biblScope unit="volume">73</biblScope>
<biblScope unit="issue">1-2</biblScope>
<biblScope unit="page" from="10">10</biblScope>
<biblScope unit="page" to="22">22</biblScope>
</imprint>
<idno type="ISSN">0022-2844</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0022-2844</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Homochirality</term>
<term>Molecular evolution</term>
<term>Proto-anti-codons</term>
<term>RNA world</term>
<term>Ribozymes</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: All living organisms encode the 20 natural amino acid units of polypeptides using a universal scheme of triplet nucleotide “codons”. Disparate features of this codon scheme are potentially informative of early molecular evolution: (i) the absence of any codons for d-amino acids; (ii) the odd combination of alternate codon patterns for some amino acids; (iii) the confinement of synonymous positions to a codon’s third nucleotide; (iv) the use of 20 specific amino acids rather than a number closer to the full coding potential of 64; and (v) the evolutionary relationship of patterns in stop codons to amino acid codons. Here I propose a model for an ancestral proto-anti-codon RNA (pacRNA) auto-aminoacylation system and show that pacRNAs would naturally manifest features of the codon table. I show that pacRNAs could implement all the steps for auto-aminoacylation: amino acid coordination, intermediate activation of the amino acid by the 5′-end of the pacRNA, and 3′-aminoacylation of the pacRNA. The anti-codon cradles of pacRNAs would have been able to recognize and coordinate only a small number of l-amino acids via hydrogen bonding. A need for proper spatial coordination would have limited the number of chargeable amino acids for all anti-codon sequences, in addition to making some anti-codon sequences unsuitable. Thus, the pacRNA model implies that the idiosyncrasies of the anti-codon table and l-amino acid homochirality co-evolved during a single evolutionary period. These results further imply that early life consisted of an aminoacylated RNA world with a richer enzymatic potential than ribonucleotides alone.</div>
</front>
</TEI>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002623 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 002623 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    MersV1
   |flux=    Main
   |étape=   Merge
   |type=    RBID
   |clé=     ISTEX:40AC08D061A237AD2B4F8868FD55DA8B82A692AE
   |texte=   A Model of Proto-Anti-Codon RNA Enzymes Requiring l -Amino Acid Homochirality
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Mon Apr 20 23:26:43 2020. Site generation: Sat Mar 27 09:06:09 2021