Starboard Tack wrote:
I don't belief I said that Shapiro's work disproved a bottom up approach to OOL research. In fact, his work was directed at the only alternative to replication first for an origin - metabolism first - which is another bottom up proposal dependent on chemical evolution. As I believe William Schopf stated, if replication first can't work, and metabolism first can't work, then you're stuck with Intelligent Design (horror of horrors.) Unfortunately, neither proposal seems to be able to be made to work, although perhaps we will one day discover the chemical process that can't be made to happen under controlled conditions in the lab supervised by brilliant minds that can occur in a mud puddle. Can't wait.
Incidentally, if you look into Dr. Shapiro's work, you'll find it dependent on the existence of a cell membrane. Just as we know that the cell is no simple blob of protoplasm, we now know this simple entity doesn't look so simple anymore, and figuring out how it could come into existence on primordial earth so the rest of a metabolism first model can work is looking less likely the more we learn about how such membranes are sturtured and function.
Examining the various proposed models of abiogenesis is interesting stuff, but likely beyond the scope of this forum. Theres almost certainly a natural process by which the first replicating molecules appeared on earth. Perhaps we shouldnt get too bogged down over which hypothesis currently has more support?
That would be a metaphysical, not a scientific statement, equivalent to my saying "there's almost certainly no natural process by which the first replicating molecule appeared on earth." The difference would be that my metaphysical statement would have scientific backing, while yours appears to be wishful thinking, given the state of OOL research.
And remember the Crick paper? Here are some more which support exactly what I was saying.
http://www.ncbi.nlm.nih.gov/pubmed/15764708
J Theor Biol. 2005 Apr 21;233(4):527-32. Epub 2004 Dec 29.
The triplet genetic code had a doublet predecessor.
Patel A.
Source
Centre for High Energy Physics and Supercomputer Education and Research Centre, Indian Institute of Science, Bangalore 560012, India.
adpatelcts.iisc.ernet.in
Abstract
Information theoretic analysis of genetic languages indicates that the naturally occurring 20 amino acids and the triplet genetic code arose by duplication of 10 amino acids of class-II and a doublet genetic code having codons NNY and anticodons GNN. Evidence for this scenario is presented based on the properties of aminoacyl-tRNA synthetases, amino acids and nucleotide bases.
www.ncbi.nlm.nih.gov/pubmed/16059752?or ... rom=pubmed
Evolution of the genetic triplet code via two types of doublet codons.
Wu HL, Bagby S, van den Elsen JM.
Source
Department of Biology and Biochemistry, University of Bath, 4 South, Claverton Down, Bath BA2 7AY, UK.
Erratum in
J Mol Evol. 2006 Sep;63(3):426.
Abstract
Explaining the apparent non-random codon distribution and the nature and number of amino acids in the 'standard' genetic code remains a challenge, despite the various hypotheses so far proposed. In this paper we propose a simple new hypothesis for code evolution involving a progression from singlet to doublet to triplet codons with a reading mechanism that moves three bases each step. We suggest that triplet codons gradually evolved from two types of ambiguous doublet codons, those in which the first two bases of each three-base window were read ('prefix' codons) and those in which the last two bases of each window were read ('suffix' codons). This hypothesis explains multiple features of the genetic code such as the origin of the pattern of four-fold degenerate and two-fold degenerate triplet codons, the origin of its error minimising properties, and why there are only 20 amino acids.
www.ncbi.nlm.nih.gov/pubmed/15748913?or ... logdbfrom=
Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4442-7. Epub 2005 Mar 11.
A mechanism for the association of amino acids with their codons and the origin of the genetic code.
Copley SD, Smith E, Morowitz HJ.
Source
Cooperative Institute for Research in Environmental Sciences, Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
shelleycires.colorado.au
Abstract
The genetic code has certain regularities that have resisted mechanistic interpretation. These include strong correlations between the first base of codons and the precursor from which the encoded amino acid is synthesized and between the second base of codons and the hydrophobicity of the encoded amino acid. These regularities are even more striking in a projection of the modern code onto a simpler code consisting of doublet codons encoding a set of simple amino acids. These regularities can be explained if, before the emergence of macromolecules, simple amino acids were synthesized in covalent complexes of dinucleotides with alpha-keto acids originating from the reductive tricarboxylic acid cycle or reductive acetate pathway. The bases and phosphates of the dinucleotide are proposed to have enhanced the rates of synthetic reactions leading to amino acids in a small-molecule reaction network that preceded the RNA translation apparatus but created an association between amino acids and the first two bases of their codons that was retained when translation emerged later in evolution.
http://nar.oxfordjournals.org/cgi/conte ... 27/17/3389
Did DNA replication evolve twice independently?
Detlef D. Leipe, L. Aravind1 and Eugene V. Koonin
DNA replication is central to all extant cellular organisms. There are substantial functional similarities between the bacterial and the archaeal/eukaryotic replication machineries, including but not limited to defined origins, replication bidirectionality, RNA primers and leading and lagging strand synthesis. However, several core components of the bacterial replication machinery are unrelated or only distantly related to the functionally equivalent components of the archaeal/eukaryotic replication apparatus. This is in sharp contrast to the principal proteins involved in transcription and translation, which are highly conserved in all divisions of life. We performed detailed sequence comparisons of the proteins that fulfill indispensable functions in DNA replication and classified them into four main categories with respect to the conservation in bacteria and archaea/eukaryotes: (i) non-homologous, such as replicative polymerases and primases; (ii) containing homologous domains but apparently non-orthologous and conceivably independently recruited to function in replication, such as the principal replicative helicases or proofreading exonucleases; (iii) apparently orthologous but poorly conserved, such as the sliding clamp proteins or DNA ligases; (iv) orthologous and highly conserved, such as clamp-loader ATPases or 35 exonucleases (FLAP nucleases). The universal conservation of some components of the DNA replication machinery and enzymes for DNA precursor biosynthesis but not the principal DNA polymerases suggests that the last common ancestor (LCA) of all modern cellular life forms possessed DNA but did not replicate it the way extant cells do. We propose that the LCA had a genetic system that contained both RNA and DNA, with the latter being produced by reverse transcription. Consequently, the modern-type system for double-stranded DNA replication likely evolved independently in the bacterial and archaeal/eukaryotic lineages.