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Hello Jery,
DNA is a negatively charged polymer that is made up of nucleotide building blocks. Before we discuss where its negative charge comes from, let’s take a close-up view of the nucleotide monomers that make up DNA.
Four different nucleotides are covalently linked to build DNA molecules: adenine (A), guanine (G), cytosine (C), and thymine (T). Each nucleotide consists of a phosphate group, a deoxyribose sugar group, and a nitrogenous base. Nucleotides are covalently linked to one another via the formation of phosphodiester bonds between the sugar group of one nucleotide and the phosphate group of a second nucleotide.
As you likely know, most DNA is found in a double-stranded form with complementary base pairing between the two DNA strands: A pairs with T, and C pairs with G. The formation of phosphodiester bonds between adjacent nucleotides forms alternating sugar and phosphate groups, called the “sugar-phosphate backbone” of a DNA molecule. Furthermore, DNA forms a double helix. In a nutshell, the structure of DNA can be thought of as a twisted ladder with its complementary base pairs making up the rungs of the ladder and the sugar-phosphate backbone of each strand making up each side of the ladder.
So, where does DNA’s negative charge come from? The phosphate groups that make up the sugar-phosphate backbone are responsible. You might be interested to read that molecular biologists capitalize on this property of DNA to isolate DNA fragments of differing sizes. Because DNA is negatively charged, molecular biologists often use agarose gel electrophoresis to separate different sized DNA fragments when DNA samples are subjected to an electric field — due to their negative charge, all of the DNA fragments will migrate toward the positively charged electrode, but smaller DNA fragments will migrate at a faster pace than larger DNA fragments. This simple, yet powerful, technique allows researchers to isolate DNA fragments of different sizes.
Supercoiling is a term used to describe what happens when the two strands of a double-stranded, double helical DNA molecule are separated from each other, which occurs during DNA replication and transcription. One way to visualize supercoiling is to think about what happens when you twist a rubber band and then hold onto one end of it while trying to open it in the middle — the original coils will twist on top of each other to form a condensed, twisted ball. This is what supercoiling is like.
Prokaryotic and eukaryotic chromosomal DNA is organized in different ways. Due to the circular nature of most prokaryotic chromosomes, they are often highly supercoiled under normal growth conditions. In contrast, eukaryotic chromosomes are linear and packaged using histone proteins, which are not present in most prokaryotic cells. As a result, eukaryotic chromosomes are not nearly as supercoiled as prokaryotic chromosomes. Intriguingly, genomes can be negatively supercoiled, (i.e., the DNA is twisted in the opposite direction of the double helix) or positively supercoiled (i.e., the DNA is twisted in the same direction as the double helix). We encourage you to follow the links we’ve provided below to learn more about this fascinating process.
For more information about DNA and its nucleotide building blocks, check out these links:
http://www.nature.com/scitable/topicpage/dna-is-a-structure-that-encodes-biological-6493050
http://www.nature.com/scitable/topicpage/discovery-of-the-function-of-dna-resulted-6494318
http://www.nature.com/scitable/topicpage/Discovery-of-DNA-Structure-and-Function-Watson-397
http://nobelprize.org/educational_games/medicine/dna_double_helix/readmore.html
To learn more about DNA supercoiling and DNA packaging, follow these links:
http://www.nature.com/scitable/topicpage/genome-packaging-in-prokaryotes-the-circular-chromosome-9113
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=mboc4&part=A975&rendertype=figure&id=A1006
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=mcb&part=A802#A818
http://www.nature.com/scitable/topicpage/dna-packaging-nucleosomes-and-chromatin-310
To learn more about agarose gel electrophoresis, check out these links:
http://www.nature.com/scitable/content/gel-electrophoresis-can-be-used-to-separate-44970
http://learn.genetics.utah.edu/content/labs/gel/
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Nature Education
Sep 09, 2010 08:57AM