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rjedlicka rjedlicka
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Posts: 97
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12 years ago
and What are the factors that affect abnrmalities/mistaken identity during the central dogma?
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wrote...
12 years ago
RNA polymerase and RNA transcription fidelity
http://7thspace.com/headlines/343669/stepwise_mechanism_for_transcription_fidelity.html
RNA polymerase works with TFIIS to transcribe RNA true to the DNA sequences
http://www.pnas.org/content/93/24/13677.abstract

RNA intron removal & exon splicing has a means to determine incorrect intron lariats. The spliceosomal ATPase Prp16 assists with fidelity of splicing RNA.
http://www.ncbi.nlm.nih.gov/pubmed/8324826
http://molbio.bsd.uchicago.edu/Faculty_and_Research/01_Faculty_Alphabetically.php?faculty_id=157
http://www.nature.com/nsmb/journal/v13/n6/full/nsmb0606-472.html

Research is ongoing to determine the ribosomes editor/proofreading mechanism  for detecting incorrect tRNA insertions and aborting the protein in progress. Dr Green says, "in the event of miscoding, the ribosome cuts the bond and aborts the protein-in-progress"
http://www.sciencedaily.com/releases/2009/01/090107134529.htm
http://www.ncbi.nlm.nih.gov/pubmed/6348473

The central dogma is that the sequences are copied to RNA and translated to protein in a sequence specific manner in one direction only; DNA -> RNA -> protein. There is no mechanism to read the sequences of the amino acids, create an RNA from this reading and move this back into the nucleus to reverse transcribe into DNA.
http://en.wikipedia.org/wiki/Central_dogma_of_molecular_biology
Reverse transcription RNA -> DNA does exist in RNA viruses but due to the degeneracy of the code there is no way to read  amino acid residues and know which of the alternate codes to use to get the original sequence. Only  methionine and tryptophan have single codons the rest have multiple so this offers no way to check for errors in the RNA.
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