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Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences
During the origin of life, the biological information of nucleic acid polymers must have increased to encode functional molecules (the RNA world). Ribozymes tend to be compositionally unbiased, as is the vast majority of possible sequence space. However, ribonucleotides vary greatly in synthetic yie...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378899/ https://www.ncbi.nlm.nih.gov/pubmed/22319215 http://dx.doi.org/10.1093/nar/gks065 |
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author | Derr, Julien Manapat, Michael L. Rajamani, Sudha Leu, Kevin Xulvi-Brunet, Ramon Joseph, Isaac Nowak, Martin A. Chen, Irene A. |
author_facet | Derr, Julien Manapat, Michael L. Rajamani, Sudha Leu, Kevin Xulvi-Brunet, Ramon Joseph, Isaac Nowak, Martin A. Chen, Irene A. |
author_sort | Derr, Julien |
collection | PubMed |
description | During the origin of life, the biological information of nucleic acid polymers must have increased to encode functional molecules (the RNA world). Ribozymes tend to be compositionally unbiased, as is the vast majority of possible sequence space. However, ribonucleotides vary greatly in synthetic yield, reactivity and degradation rate, and their non-enzymatic polymerization results in compositionally biased sequences. While natural selection could lead to complex sequences, molecules with some activity are required to begin this process. Was the emergence of compositionally diverse sequences a matter of chance, or could prebiotically plausible reactions counter chemical biases to increase the probability of finding a ribozyme? Our in silico simulations using a two-letter alphabet show that template-directed ligation and high concatenation rates counter compositional bias and shift the pool toward longer sequences, permitting greater exploration of sequence space and stable folding. We verified experimentally that unbiased DNA sequences are more efficient templates for ligation, thus increasing the compositional diversity of the pool. Our work suggests that prebiotically plausible chemical mechanisms of nucleic acid polymerization and ligation could predispose toward a diverse pool of longer, potentially structured molecules. Such mechanisms could have set the stage for the appearance of functional activity very early in the emergence of life. |
format | Online Article Text |
id | pubmed-3378899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33788992012-06-20 Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences Derr, Julien Manapat, Michael L. Rajamani, Sudha Leu, Kevin Xulvi-Brunet, Ramon Joseph, Isaac Nowak, Martin A. Chen, Irene A. Nucleic Acids Res Synthetic Biology and Chemistry During the origin of life, the biological information of nucleic acid polymers must have increased to encode functional molecules (the RNA world). Ribozymes tend to be compositionally unbiased, as is the vast majority of possible sequence space. However, ribonucleotides vary greatly in synthetic yield, reactivity and degradation rate, and their non-enzymatic polymerization results in compositionally biased sequences. While natural selection could lead to complex sequences, molecules with some activity are required to begin this process. Was the emergence of compositionally diverse sequences a matter of chance, or could prebiotically plausible reactions counter chemical biases to increase the probability of finding a ribozyme? Our in silico simulations using a two-letter alphabet show that template-directed ligation and high concatenation rates counter compositional bias and shift the pool toward longer sequences, permitting greater exploration of sequence space and stable folding. We verified experimentally that unbiased DNA sequences are more efficient templates for ligation, thus increasing the compositional diversity of the pool. Our work suggests that prebiotically plausible chemical mechanisms of nucleic acid polymerization and ligation could predispose toward a diverse pool of longer, potentially structured molecules. Such mechanisms could have set the stage for the appearance of functional activity very early in the emergence of life. Oxford University Press 2012-05 2012-02-07 /pmc/articles/PMC3378899/ /pubmed/22319215 http://dx.doi.org/10.1093/nar/gks065 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Synthetic Biology and Chemistry Derr, Julien Manapat, Michael L. Rajamani, Sudha Leu, Kevin Xulvi-Brunet, Ramon Joseph, Isaac Nowak, Martin A. Chen, Irene A. Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences |
title | Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences |
title_full | Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences |
title_fullStr | Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences |
title_full_unstemmed | Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences |
title_short | Prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences |
title_sort | prebiotically plausible mechanisms increase compositional diversity of nucleic acid sequences |
topic | Synthetic Biology and Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378899/ https://www.ncbi.nlm.nih.gov/pubmed/22319215 http://dx.doi.org/10.1093/nar/gks065 |
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