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Page "Molecular genetics" ¶ 16
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DNA and nucleotides
* Base pair, a pair of connected nucleotides on complementary DNA and RNA strands
Instead it generates the sequences of many thousands of small DNA fragments ( ranging from 35 to 900 nucleotides long, depending on the sequencing technology ).
Chemical analogs of nucleotides can take the place of proper nucleotides and establish non-canonical base-pairing, leading to errors ( mostly point mutations ) in DNA replication and DNA transcription.
Other chemicals, known as DNA intercalators, fit into the gap between adjacent bases on a single strand and induce frameshift mutations by " masquerading " as a base, causing the DNA replication machinery to skip or insert additional nucleotides at the intercalated site.
For case of single stranded DNA / RNA units of nucleotides are used, abbreviated nt ( or knt, Mnt, Gnt ), as they are not paired.
This is DNA which contains units named genes that can produce proteins through a code ( genetic code ) in which a series of triplets ( codons ) of four possible nucleotides are translated into one of twenty possible amino acids.
The DNA molecule may be circular or linear, and can be composed of 100, 000 to over 3, 750, 000, 000 nucleotides in a long chain.
DNA consists of two long polymers of simple units called nucleotides, with backbones made of sugars and phosphate groups joined by ester bonds.
DNA is a long polymer made from repeating units called nucleotides.
Although each individual repeating unit is very small, DNA polymers can be very large molecules containing millions of nucleotides.
Polymers comprising multiple linked nucleotides ( as in DNA ) are called a polynucleotide.
The DNA double helix is stabilized primarily by two forces: hydrogen bonds between nucleotides and base-stacking interactions among the aromatic nucleobases.
In addition to DNA polymerase, the enzyme that synthesizes the new DNA by adding nucleotides matched to the template strand, a number of other proteins are associated with the fork and assist in the initiation and continuation of DNA synthesis.
Each single strand of DNA is a chain of four types of nucleotides having the bases: adenine, cytosine, guanine, and thymine ( commonly noted as A, C, G & T ).
Chemical interaction of these nucleotides forms phosphodiester linkages, creating the phosphate-deoxyribose backbone of the DNA double helix with the bases pointing inward.
Directionality has consequences in DNA synthesis, because DNA polymerase can synthesize DNA in only one direction by adding nucleotides to the 3 ' end of a DNA strand.

DNA and are
The order is clearly circumscribed on the basis of DNA sequence analysis, but is difficult to define morphologically, since its members are structurally diverse.
Abzymes are usually artificial constructs, but are also found in normal humans ( anti-vasoactive intestinal peptide autoantibodies ) and in patients with autoimmune diseases such as systemic lupus erythematosus, where they can bind to and hydrolyze DNA.
Abzymes are potential tools in biotechnology, e. g., to perform specific actions on DNA.
It is now known that each of the A, B, and O alleles is actually a class of multiple alleles with different DNA sequences that produce proteins with identical properties: more than 70 alleles are known at the ABO locus.
Genetic fingerprinting and DNA microarray are very popular tools and research fields.
Nucleic acids are the molecules that make up DNA, an extremely important substance that all cellular organisms use to store their genetic information.
The most common nucleic acids are deoxyribonucleic acid ( DNA ) and ribonucleic acid ( RNA ).
Also, the nitrogenous bases possible in the two nucleic acids are different: adenine, cytosine, and guanine occur in both RNA and DNA, while thymine occurs only in DNA and uracil occurs in RNA.
All organisms have cells, the cell types are unique and their nuclei store most of the DNA.
These programs can compensate for mutations ( exchanged, deleted or inserted bases ) in the DNA sequence, to identify sequences that are related, but not identical.
Most current genome annotation systems work similarly, but the programs available for analysis of genomic DNA, such as the GeneMark program trained and used to find protein-coding genes in Haemophilus influenzae, are constantly changing and improving.
In molecular biology and genetics, the linking between two nitrogenous bases on opposite complementary DNA or certain types of RNA strands that are connected via hydrogen bonds is called a base pair ( often abbreviated bp ).
Paired DNA and RNA molecules are comparatively stable at room temperature but the two nucleotide strands will separate above a melting point that is determined by the length of the molecules, the extent of mispairing ( if any ), and the GC content.
Base stacking interactions in DNA and RNA are due to dispersion attraction, short-range exchange repulsion, and electrostatic interactions, which also contribute to stability.
Modern variants of the Batavian founding myth are made more credible by pointing out that the Batavians were only part of the ancestry of the Dutch people, together with the Frisians, Franks and Saxons, and by tracing patterns of DNA.
DNA analysis recently revealed that the identified subspecies of brown bears, both Eurasian and North American, are genetically quite homogeneous, and that their genetic phylogeography does not correspond to their traditional taxonomy.
Though there is some debate on the exact mechanism of conjugation it seems that the pili are not the structures through which DNA exchange occurs.
This has been shown in experiments where the pilus are allowed to make contact, but then are denatured with SDS and yet DNA transformation still proceeds.
In the first type, a researcher may design short pieces of DNA (" probes ") whose sequences are complementary to the mutated sequences.
Genetic engineering, recombinant DNA technology, genetic modification / manipulation ( GM ) and gene splicing are terms that apply to the direct manipulation of an organism's genes.

DNA and base
* Nucleobase, in genetics, the parts of DNA and RNA involved in forming base pairs
In the canonical Watson-Crick DNA base pairing, adenine ( A ) forms a base pair with thymine ( T ) and guanine ( G ) forms a base pair with cytosine ( C ).
The size of an individual gene or an organism's entire genome is often measured in base pairs because DNA is usually double-stranded.
A kilobase ( kb ) is a unit of measurement in molecular biology equal to 1000 base pairs of DNA or RNA.
This enzyme operates on a single strand of mRNA, generating its complementary DNA based on the pairing of RNA base pairs ( A, U, G and C ) to their DNA complements ( T, A, C and G respectively ).
# A poly-T oligonucleotide primer is hybridized onto the poly-A tail of the mature mRNA template, or random hexamer primers can be added which contain every possible 6 base single strand of DNA and can therefore hybridize anywhere on the RNA ( Reverse transcriptase requires this double-stranded segment as a primer to start its operation.
The atoms in the structure are colour coded by Chemical element | element and the detailed structure of two base pairs are shown in the bottom right. The structure of part of a DNA double helix
Indeed, this reversible and specific interaction between complementary base pairs is critical for all the functions of DNA in living organisms.
The energy for this process of DNA polymerization comes from two of the three total phosphates attached to each unincorporated base.
As the labelled DNA molecules are separated, the fluorescent label is excited by a UV source, and the identity of the base terminating the molecule is identified by the wavelength of the emitted light.
Intercalated ethidium is in a hydrophobic environment when it is between the base pairs of the DNA, protected from quenching by water which is excluded from the local environment of the intercalated ethidium.
Additionally, base pairs in chromosomes often undergo random mutations resulting in modified DNA ( and subsequently, new proteins and phenotypes ).
Whereas a genome sequence lists the order of every DNA base in a genome, a genome map identifies the landmarks.
Genome size is the total number of DNA base pairs in one copy of a haploid genome.
Agarose gel electrophoresis can be used for the separation of DNA fragments ranging from 50 base pair to several megabases ( millions of bases ) using specialized apparatus.
George Gamow proposed that the genetic code was composed of sequences of three DNA base pairs known as triplets or codons which represent one of the twenty amino acids.
Two of each of the core histones assemble to form one octameric nucleosome core particle, and 147 base pairs of DNA wrap around this core particle 1. 65 times in a left-handed super-helical turn.
This involves the wrapping of DNA around nucleosomes with approximately 50 base pairs of DNA separating each pair of nucleosomes ( also referred to as linker DNA ).

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