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The molecular roots of compositional inheritance
1Department of Molecular Genetics and The Crown Genome Center, The Weizmann Institute of Science, Rehovot, 76100, Israel.
Journal of Theoretical Biology
|December 12, 2001
Summary
Non-covalent molecular assemblies offer a primitive inheritance mechanism. High reproduction fidelity depends on lognormal catalytic rates and optimal assembly size, crucial for early life evolution.
Area of Science:
- Origin of Life Research
- Systems Chemistry
- Biophysics
Background:
- Non-covalent compositional assemblies present an alternative inheritance mechanism to biopolymers.
- These assemblies are central to
- Metabolism First
- origin of life scenarios and the Graded Autocatalysis Replication Domain (GARD) model.
Purpose of the Study:
- To analyze the quantitative molecular basis of inheritance in non-covalent assemblies.
- To define conditions favoring high reproduction fidelity in early pre-biotic systems.
Main Methods:
- Development of a novel heritability measure, eta(*)(s).
- Analysis of the dependence of reproduction fidelity on molecular recognition parameters and assembly size.
- Investigating the impact of different distributions (normal vs. lognormal) of catalytic rate acceleration coefficients.
Main Results:
- Reproduction fidelity (eta(*)(s)) is sensitive to molecular recognition parameters and assembly size.
- Normal distribution of catalytic rates leads to
- compositional error catastrophes
- , preventing information transfer.
- Lognormal distribution of catalytic rates, consistent with statistical formalisms, yields high reproduction fidelity.
- Optimal assembly size for maximal fidelity is approximately 3.5 N(G)/lambda.
Conclusions:
- The distribution of catalytic rates and assembly size are critical factors for pre-biotic inheritance.
- Lognormal distributions of catalytic rates are essential for high-fidelity information transfer in early life.
- These findings delineate physicochemical conditions conducive to the emergence of pre-biotic evolution.