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The equalities G = C and A = T suggested that these bases were paired, this pairing being the basis of the DNA structure that is now known to be correct. Conversely the inequalities G ≠ A etc. meant that DNA could not have a systematic repetition of a fundamental unit, as required by the tetranucleotide hypothesis.
The split gene theory is a theory of the origin of introns, long non-coding sequences in eukaryotic genes between the exons. [1] [2] [3] The theory holds that the randomness of primordial DNA sequences would only permit small (< 600bp) open reading frames (ORFs), and that important intron structures and regulatory sequences are derived from stop codons.
The details of how sequences of DNA instruct cells to make specific proteins was worked out by molecular biologists during the period from 1953 to 1965. Francis Crick played an integral role in both the theory and analysis of the experiments that led to an improved understanding of the genetic code. [6]
DNA sequencing is the process of determining the nucleotide sequence of a given DNA fragment. The sequence of the DNA of a living thing encodes the necessary information for that living thing to survive and reproduce. Therefore, determining the sequence is useful in fundamental research into why and how organisms live, as well as in applied ...
DNA structure and bases A-B-Z-DNA Side View. Tertiary structure refers to the locations of the atoms in three-dimensional space, taking into consideration geometrical and steric constraints. It is a higher order than the secondary structure, in which large-scale folding in a linear polymer occurs and the entire chain is folded into a specific 3 ...
Therefore in this book I will consider genes as DNA sequences encoding information for functional products, be it proteins or RNA molecules. With 'encoding information', I mean that the DNA sequence is used as a template for the production of an RNA molecule or a protein that performs some function. [5]
The structure of the DNA double helix (type B-DNA). The atoms in the structure are color-coded by element and the detailed structures of two base pairs are shown in the bottom right. DNA exists as a double-stranded structure, with both strands coiled together to form the characteristic double helix.
DNA that never existed before can be observed in the chromosomes, such as horizontal gene transfer of DNA or viral integration. If the chromosomes become different enough, evolution can form a new species. Substitutions that alter a single base pair are individually invisible and substitutions occur at a finite rate per site.