Talk:Genetic code

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Theories on the origin of the genetic code

Despite the variations that exist, the genetic codes used by all known forms of life on Earth are very similar. Since there are many possible genetic codes that are thought to have similar utility to the one used by Earth life, the theory of evolution suggests that the genetic code was established very early in the history of life and meta-analysis of transfer RNA suggest it was established soon after the formation of earth.

One can ask the question: is the genetic code completely random, just one set of codon-amino acid correspondences that happened to establish itself and be "frozen in" early in evolution, although functionally any of the many other possible transcription tables would have done just as well? Already a cursory look at the table shows patterns that suggest that this is not the case. For example, C in 2nd position of the codon yields amino acid residues that are small in size and moderate in

hydropathy; U in 2nd position encodes average size hydrophobic residues; A in 2nd position encodes average size hydrophilic residues; U in 1st position encodes residues that are not hydrophilic, see Image:Codon_Bias.jpg, adapted from http://www.complexity.org.au/ci/vol01/fullen01/html
] and (Yang et al. 1990. In Reaction Centers of Photosynthetic Bacteria. M.-E. Michel-Beyerle. (Ed.) (Springer-Verlag, Germany) 209-218).

There are three themes running through the many theories that seek to explain the evolution of the genetic code (and hence the origin of these patterns).

.

References

  1. ^ Knight, R.D.; Freeland S. J. and Landweber, L.F. (1999) The 3 Faces of the Genetic Code. Trends in the Biochemical Sciences 24(6), 241-247.
  2. ^ Knight, R.D. and Landweber, L.F. (1998). Rhyme or reason: RNA-arginine interactions and the genetic code. Chemistry & Biology 5(9), R215-R220. PDF version of manuscript
  3. ^ Brooks, Dawn J.; Fresco, Jacques R.; Lesk, Arthur M.; and Singh, Mona. (2002). Evolution of Amino Acid Frequencies in Proteins Over Deep Time: Inferred Order of Introduction of Amino Acids into the Genetic Code. Molecular Biology and Evolution 19, 1645-1655.
  4. ^ Amirnovin R. (1997) An analysis of the metabolic theory of the origin of the genetic code. Journal of Molecular Evolution 44(5), 473-6.
  5. ^ Ronneberg T.A.; Landweber L.F. and Freeland S.J. (2000) Testing a biosynthetic theory of the genetic code: Fact or artifact? Proceedings of the National Academy of Sciences, USA 97(25), 13690-13695.
  6. ^ Freeland S.J.; Wu T. and Keulmann N. (2003) The Case for an Error Minimizing Genetic Code. Orig Life Evol Biosph. 33(4-5), 457-77.

Codon table layout

Until several weeks ago the codon table in this article looked like this:

Former codon table

2nd base
U C A G
1st
base
U UUU (Phe/F) Phenylalanine

UUC (Phe/F) Phenylalanine

UCU (Ser/S) Serine

UCC (Ser/S) Serine

UAU (Tyr/Y) Tyrosine

UAC (Tyr/Y) Tyrosine

UGU (Cys/C) Cysteine

UGC (Cys/C) Cysteine

UUA (Leu/L) Leucine UCA (Ser/S) Serine UAA Ochre (Stop) UGA Opal (Stop)
UUG (Leu/L) Leucine UCG (Ser/S) Serine UAG Amber (Stop) UGG (Trp/W) Tryptophan
C CUU (Leu/L) Leucine

CUC (Leu/L) Leucine

CCU (Pro/P) Proline

CCC (Pro/P) Proline

CAU (His/H) Histidine

CAC (His/H) Histidine

CGU (Arg/R) Arginine

CGC (Arg/R) Arginine

CUA (Leu/L) Leucine

CUG (Leu/L) Leucine

CCA (Pro/P) Proline

CCG (Pro/P) Proline

CAA (Gln/Q) Glutamine

CAG (Gln/Q) Glutamine

CGA (Arg/R) Arginine

CGG (Arg/R) Arginine

A AUU (Ile/I) Isoleucine

AUC (Ile/I) Isoleucine

ACU (Thr/T) Threonine

ACC (Thr/T) Threonine

AAU (Asn/N) Asparagine

AAC (Asn/N) Asparagine

AGU (Ser/S) Serine

AGC (Ser/S) Serine

AUA (Ile/I) Isoleucine ACA (Thr/T) Threonine AAA (Lys/K) Lysine AGA (Arg/R) Arginine
AUG[A] (Met/M) Methionine
ACG (Thr/T) Threonine AAG (Lys/K) Lysine AGG (Arg/R) Arginine
G GUU (Val/V) Valine

GUC (Val/V) Valine

GCU (Ala/A) Alanine

GCC (Ala/A) Alanine

GAU (Asp/D) Aspartic acid

GAC (Asp/D) Aspartic acid

GGU (Gly/G) Glycine

GGC (Gly/G) Glycine

GUA (Val/V) Valine

GUG (Val/V) Valine

GCA (Ala/A) Alanine

GCG (Ala/A) Alanine

GAA (Glu/E) Glutamic acid

GAG (Glu/E) Glutamic acid

GGA (Gly/G) Glycine

GGG (Gly/G) Glycine

An IP changed it to the following:

Current codon table

2nd base
U C A G
1st
base
U
UUU (Phe/F)
Phenylalanine
UUC (Phe/F)
Phenylalanine
UUA (Leu/L)
Leucine
UUG (Leu/L)
Leucine
UCU (Ser/S)
Serine
UCC (Ser/S)
Serine
UCA (Ser/S)
Serine
UCG (Ser/S)
Serine
UAU (Tyr/Y)
Tyrosine
UAC (Tyr/Y)
Tyrosine
UAA Ochre
Stop
UAG Amber
Stop
UGU (Cys/C)
Cysteine
UGC (Cys/C)
Cysteine
UGA Opal
Stop
UGG (Trp/W)
Tryptophan
C
CUU (Leu/L)
Leucine
CUC (Leu/L)
Leucine
CUA (Leu/L)
Leucine
CUG (Leu/L)
Leucine
CCU (Pro/P)
Proline
CCC (Pro/P)
Proline
CCA (Pro/P)
Proline
CCG (Pro/P)
Proline
CAU (His/H)
Histidine
CAC (His/H)
Histidine
CAA (Gln/Q)
Glutamine
CAG (Gln/Q)
Glutamine
CGU (Arg/R)
Arginine
CGC (Arg/R)
Arginine
CGA (Arg/R)
Arginine
CGG (Arg/R)
Arginine
A
AUU (Ile/I)
Isoleucine
AUC (Ile/I)
Isoleucine
AUA (Ile/I)
Isoleucine
AUG [A] (Met/M)
Methionine
ACU (Thr/T)
Threonine
ACC (Thr/T)
Threonine
ACA (Thr/T)
Threonine
ACG (Thr/T)
Threonine
AAU (Asn/N)
Asparagine
AAC (Asn/N)
Asparagine
AAA (Lys/K)
Lysine
AAG (Lys/K)
Lysine
AGU (Ser/S)
Serine
AGC (Ser/S)
Serine
AGA (Arg/R)
Arginine
AGG (Arg/R)
Arginine
G
GUU (Val/V)
Valine
GUC (Val/V)
Valine
GUA (Val/V)
Valine
GUG (Val/V)
Valine
GCU (Ala/A)
Alanine
GCC (Ala/A)
Alanine
GCA (Ala/A)
Alanine
GCG (Ala/A)
Alanine
GAU (Asp/D)
Aspartic acid
GAC (Asp/D)
Aspartic acid
GAA (Glu/E)
Glutamic acid
GAG (Glu/E)
Glutamic acid
GGU (Gly/G)
Glycine
GGC (Gly/G)
Glycine
GGA (Gly/G)
Glycine
GGG (Gly/G)
Glycine

This was reverted a few times, until the IP (editing from 220.253.25.118) explained the change: "codons are not polar etc but amino acids are." In other words, the color scheme applies to the amino acids, not the codons, so the colored shading should not be applied to the codons themselves. I agree with this reasoning. The problems with this table are that (1) As noted above, it's very bulky, and (2) Consequently, it obscures the non-random nature of the genetic code – the tendency for single-base substitutions to result in codons with similar chemical properties. In the sandbox, 220.253.25.118 created a new table which I think combines the best features of both other tables: it does not apply color shading to the codons, it's compact, and the non-random nature of the code is readily apparent. I've applied minor tweaks to this table, and the result is below:

220.253.25.118's table, tweaked

  2nd base
U C A G
1st base U UUU (Phe/F) Phenylalanine UCU (Ser/S) Serine UAU (Tyr/Y) Tyrosine UGU (Cys/C) Cysteine
UUC (Phe/F) Phenylalanine UCC (Ser/S) Serine UAC (Tyr/Y) Tyrosine UGC (Cys/C) Cysteine
UUA (Leu/L) Leucine UCA (Ser/S) Serine UAA Ochre (Stop) UAG Opal (Stop)
UUG (Leu/L) Leucine UCG (Ser/S) Serine UAG Amber (Stop) UGG (Trp/W) Tryptophan
C CUU (Leu/L) Leucine CCU (Pro/P) Proline CAU (His/H) Histidine CGU (Arg/R) Arginine
CUC (Leu/L) Leucine CCC (Pro/P) Proline CAC (His/H) Histidine CGC (Arg/R) Arginine
CUA (Leu/L) Leucine CCA (Pro/P) Proline CAA (Gln/Q) Glutamine CGA (Arg/R) Arginine
CUG (Leu/L) Leucine CCG (Pro/P) Proline CAG (Gln/Q) Glutamine CGG (Arg/R) Arginine
A AUU (Ile/I) Isoleucine ACU (Thr/T) Threonine AAU (Asn/N) Asparagine AGU (Ser/S) Serine
AUC (Ile/I) Isoleucine ACC (Thr/T) Threonine AAC (Asn/N) Asparagine AGC (Ser/S) Serine
AUA (Ile/I) Isoleucine ACA (Thr/T) Threonine AAA (Lys/K) Lysine AGA (Arg/R) Arginine
AUG[A] (Met/M) Methionine ACG (Thr/T) Threonine AAG (Lys/K) Lysine AGG (Arg/R) Arginine
G GUU (Val/V) Valine GCU (Ala/A) Alanine GAU (Asp/D) Aspartic acid GGU (Gly/G) Glycine
GUC (Val/V) Valine GCC (Ala/A) Alanine GAC (Asp/D) Aspartic acid GGC (Gly/G) Glycine
GUA (Val/V) Valine GCA (Ala/A) Alanine GAA (Glu/E) Glutamic acid GGA (Gly/G) Glycine
GUG (Val/V) Valine GCG (Ala/A) Alanine GAG (Glu/E) Glutamic acid GGG (Gly/G) Glycine

I'm not sure why 220.253.25.118 didn't incorporate this into the article, but if there's no objection I'd like to replace the current table with this one. Adrian J. Hunter(talkcontribs) 11:21, 11 September 2010 (UTC)[reply]

Support. Looks like an improvement in the current (making trends more apparent and table less bulky) while still retaining the valid polarity concern of the IP. An alternative solution is to simply clearly state in the table legend or intro that the coloring refers to the amino acid polarity, not just "polarity". The IP-current and Adrian's improvements still make horizontal (second-base for constant first and third) trends harder to notice (though obviously no 2D table can alow all three base-positions' comparisons by adjacency). DMacks (talk) 15:55, 11 September 2010 (UTC)[reply]
I see what you mean about the second base trends, though those are weaker than for the other bases anyway (2nd base changes are never synonymous). For now I've changed the table to the third option as the first option uses horizontal lines inconsistently (eg look at the lines between leucines), but I wouldn't object to coloring of the codons if someone wants to implement it. Maybe one day someone will present the table as a 4x4x4 Borg cube that shows all trends equally :-) Adrian J. Hunter(talkcontribs) 11:59, 19 September 2010 (UTC)[reply]
Just so you have something to look forward to, that was added to the article a while ago and looks great! We also have developed time-travel. DMacks (talk) 12:25, 19 September 3010 (UTC)[reply]
Would be cool if there were a VR or at least user-rotatable-3D format supported. DMacks (talk) 12:25, 19 September 2010 (UTC)[reply]

DNA codon table, E. coli usage

yellow, nonpolar g-Yellow, Trp green-yellow, Tyr green, polar green-blue, His blue, basic red, acidic (stop codon)
  2nd base
T C A G
1st base T TTT 0.57 Phe / F TCT 0.11 Ser / S TAT 0.53 Tyr / Y TGT 0.42 Cys / C
TTC 0.43 Phe / F TCC 0.11 Ser / S TAC 0.47 Tyr / Y TGC 0.58 Cys / C
TTA 0.15 Leu / L TCA 0.15 Ser / S TAA 0.64 Ochre TGA 0.36 Opal
TTG 0.12 Leu / L TCG 0.16 Ser / S TAG 0.00 Amber TGG 1.00 Trp / W
C CTT 0.12 Leu / L CCT 0.17 Pro / P CAT 0.55 His / H CGT 0.36 Arg / R
CTC 0.10 Leu / L CCC 0.13 Pro / P CAC 0.45 His / H CGC 0.44 Arg / R
CTA 0.05 Leu / L CCA 0.14 Pro / P CAA 0.30 Gln / Q CGA 0.07 Arg / R
CTG 0.46 Leu / L CCG 0.55 Pro / P CAG 0.70 Gln / Q CGG 0.07 Arg / R
A ATT 0.58 Ile / I ACT 0.16 Thr / T AAT 0.47 Asn / N AGT 0.14 Ser / S
ATC 0.35 Ile / I ACC 0.47 Thr / T AAC 0.53 Asn / N AGC 0.33 Ser / S
ATA 0.07 Ile / I ACA 0.13 Thr / T AAA 0.73 Lys / K AGA 0.02 Arg / R
ATG[A] 1 Met / M ACG 0.24 Thr / T AAG 0.27 Lys / K AGG 0.03 Arg / R
G GTT 0.25 Val / V GCT 0.11 Ala / A GAT 0.65 Asp / D GGT 0.29 Gly / G
GTC 0.18 Val / V GCC 0.31 Ala / A GAC 0.35 Asp / D GGC 0.46 Gly / G
GTA 0.17 Val / V GCA 0.21 Ala / A GAA 0.70 Glu / E GGA 0.13 Gly / G
GTG 0.40 Val / V GCG 0.38 Ala / A GAG 0.30 Glu / E GGG 0.12 Gly / G
A The codon ATG both codes for methionine and serves as an initiation site: the first ATG in the coding region is where translation into protein begins.[1]

References

  1. PMID 19056476. {{cite journal}}: Unknown parameter |month= ignored (help
    )

Codon Cluster Analysis With Hydropathy

https://www.researchgate.net/publication/374973672_Codon_Cluster_Analysis_With_Hydropathy_Written_by_GPT-4_in_Python Doug youvan (talk) 19:38, 25 October 2023 (UTC)[reply]

"using copyrighted works from others" if you are not the copyright holder of this material, or "donating copyrighted materials"
if you are.)

For

guideline on non-free text for how to properly implement limited quotations of copyrighted text. Wikipedia takes copyright violations very seriously, and persistent violators will be blocked from editing. While we appreciate contributions, we must require all contributors to understand and comply with these policies. Thank you. DanCherek (talk) 17:00, 15 March 2024 (UTC)[reply
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