| home | Biological | until 1854 | Formalization 1854-1937 | Revolutions 1937-1951 | Electronic Age |
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Location: http://members.tripod.de/s_ulf/csh/pre.html
& http://www.cs.mun.ca/~ulf/csh/pre.html.
By Ulf Schünemann since 251198.
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| DNA is a double chain (twisted to a double helix) where at each link of the chain there can be one of four nucleotide bases: adenine (A), guanine (G), thymine (T), and cytosine (C). Each half of the double chain is a template of/for the other half, where nucleotides on each side match as follows: A:T, T:A, G:C, C:G. |
| This redudancy (duplication) of information allows some kinds of repairs, and allows safer replication: The two halfs are separated, and then each one is ``repaired'' to a double chain by reconstructing its complement. This way each of the new double chains is half new and half old. «This "semiconservative" replication is the key to the stable inheritance of genetic traits» [Britannica]. |
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«There are 64 possible codons, three of which do not code for amino acids
but indicate the end of a protein. The remaining 61 codons specify the 20 amino acids
that make up proteins. The AUG codon [of mRNA], in addition to coding for methionine,
is found at the beginning of every mRNA and indicates the start of a protein ...
[T]he genetic code is identical in almost all species, with the same codons specifying the same amino acids.»
[Britannica].
Amino acids #21 (selenocystein) and #22 (pyrrolysin) were discovered 1986 and 2002 resp. [Spiegel Online 24 May 2002] |
| information (amino acid) | start protein encoding (only in bacteria), and methionine ile... | thr... | asn... lysine |
ser... arg... | his... gln... | proline | leucin
phenyl- alanine | cys... trp... | tyr...
end of encoding | serin | glycin | valine | ala... | asp... glu... tRNA anticodon
| UAC
| UAA/G/U UG*
| UUA/G | UUU/C UCA/G | UCU/C
| - | GC* GUA/G | GUU/C GG*
| GA* | -
| AAU/C
| AAA/G ACA/G | ACC AUA/G
| - AG*
| CC*
| CA*
| CG*
| CUA/G | CUU/C mRNA codon
| AUG
| AUU/C/A AC*
| AAU/C | AAA/G AGU/C | AGA/G - | CG* CAU/C | CAA/G CC*
| CU* | - UUA/G
| UUU/C UGU/C | UGG UAU/C
| UGA, UAA/G UC*
| GG*
| GU*
| GC*
| GAU/C | GAA/G DNA codogen
| TAC
| TAA/G/T TG*
| TTA/G | TTT/C TCA/G | TCT/C - | GC* GTA/G | GTT/C GG*
| GA* | - AAT/C
| AAA/G ACA/G | ACC ATA/G
| ACT, ATT/C AG*
| CC*
| CA*
| CG*
| CTA/G | CTT/C | |||||
| The brain is a chemo-electrical computer. The human brain developed in the last 3-4 million years, tripling primate brain mass and volume. In human beings, the brain is, with 2% of the body weight (1100-1800gr), 9 times as heavy as normal for mammals, and it consumes a lot of energy: The brain's metabolism is 20 times higher than that of skeletal muscles, it uses 20% of the energy taken in by nutrition, 15% of the oxygen, and 40% of the blood sugar. On the other hand, much less resources are used up for digestion: intestine mass is much smaller (just 1/2 ?) than normal for mammals (900gr). |
Larger brain made a larger head,
increasing the change for complications at birth.
The limit of head size at birth to the width of the birth channel
required humans to be born in a less mature state than normal for mammals,
ensuing the need for more (parental) care for the baby.
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Larger brain (and language) improved social skills.
Typical clan size increased to 150 members
from chimpanzes' and pavians' 50 members.
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| home | Biological | until 1854 | Formalization 1854-1937 | Revolutions 1937-1951 | Electronic Age | references
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Location: http://members.tripod.de/s_ulf/csh/cshist1.html
& http://www.cs.mun.ca/~ulf/csh/cshist1.html.
By Ulf Schünemann since 251198.
Please mail any comments.
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