Software Catagories
Home
 
Genomics

DNA

Mendel

Heredity
Bioinformatics

Genetic Engineering

DNA Testing

Genetics

Genes

Geneticists

Genetic Testing

Molecular Biology

Punnett

Phenotype

Genetic Code

Recessive
Functional Genomics
Structural Genomics
Gene Letter
Biotech
Cloning Animals
Biotechnology
Genetic Twins
Site map

Audio Books

Language


Genetic Code Information Resources

Genetic Code

Genetic code refers to the means through which information within the genetic material is translated into proteins by cells. The genome of an organism (its encoded heredity sequence) is emblazoned on the DNA or RNA. The portion of the genome, referred to as genes, code for proteins that are made of triple nucleotide units called codons.

Each codon will code for particular amino acids. The nucleotide subunits are composed of deoxyribose, phosphate and one of the following four nitrogenous nucleotide bases: adenine (A), guanine (G), cytosine (C) and thymine (T). In RNA (viruses) uracil (U) replaces thymine and ribose substitutes deoxyribose. Therefore the ‘code’ of the sequence is shown by an arrangement of four letters; either A, G, C & T in DNA or A, G, C, U in RNA. The three-letter codon was proposed by George Gamov to represent the 20 different amino acids used by living organisms to encode proteins.

In the 1950s, scientists from across the globe were in competition with one another to unlock the method by which DNA is translated into proteins. By 1961, Marshall Nirenberg claimed to have unlocked the code, and for his achievements, he was awarded the Nobel Prize. One of Nirenberg’s main challenges was to discover how many bases would be in each codon.

Scientists knew there were the four nucleotide bases of adenine (A), guanine (G), cytosine (C) and thymine (T), and also knew there were twenty known amino acids. This led them to the conclusion that there must be at least three bases in each codon (4 x 4 x 4) providing 64 possibilities.

Nirenberg pioneered a technique for testing different amino acids on cell materials. He created the ‘cell-free system’, which required him to rupture the walls of the cell so that the cytoplasm within could be released. This cytoplasm was then placed into twenty different test tubes. The cytoplasm can synthesise protein outside of the cell, but only when the correct kind of RNA is added, which allowed him to control the experiment.

Each of the twenty test tubes were filled with a different amino acid and the cytoplasm from E. Coli bacteria cells were added to these acids. One of the twenty test tubes was radioactively tagged to enable the scientists to watch the reaction. On the 27th May 1961, Nirenberg combined the cytoplasm with a synthetic RNA called poly-U (made from uracil), with the radioactively tagged tube containing phenylalanine.

The control tubes were showing a level of 70 counts per milligram of protein, whereas the phenylalanine tube was showing 38,000 counts. This experiment showed that a repeating uracil chain of bases could force a protein chain of phenylalanine (the repeating amino acid).

Even after this breakthrough experiment, there were still several tasks to be completed before the code could truly said to have been solved. The researchers still had to establish which bases make up each codon and determine the sequence of these bases in the codons.

By 1965, Nirenberg had completed the code sequencing. The letters of DNA and RNA could now be expressed in the form of a four-letter code, with groups of three letters representing individual amino acids. If mutations exist within the DNA’s code, incorrect protein formation can result
.