Deoxyribonucleic acid, better known as DNA, was first identified on a discarded surgical bandage almost 150 years ago. Increasingly sophisticated tools and techniques have allowed scientists to learn more about this chemical compound that includes all the instructions necessary for building a living organism. From among the dozens of fascinating things known about DNA, here are six items touching on the make up of DNA’s double helix, the vast amounts of DNA packed into every human’s cells, common DNA errors and a few ways DNA can repair itself.
1. DNA is in every living thing.
The chemical instructions for building a person—and every other creature on Earth—are contained in DNA. DNA is shaped like a corkscrew-twisted ladder, called a double helix. The two ladder rails are referred to as backbones, made of alternating groups of sugar and phosphate. The ladder’s rungs are made from four different building blocks called bases, arranged in pairs: adenine (A) paired with thymine (T), and cytosine (C) paired with guanine (G). Humans have about 3 billion base pairs in each cell. The order of the base pairs determines the exact instructions encoded in that part of the DNA molecule. Also, the sequence of DNA base pairs in one person is about 99.9 percent identical to that of everyone else.
2. Humans have a lot of DNA.
Humans begin as a single fertilized cell containing (with some rare exceptions) the full complement of DNA—the genome—arranged into 46 discrete chromosomes (23 pairs, with mom and dad each contributing half of each pair) in the cell’s nucleus. There are 6 feet of DNA coiled up tightly in that first cell. All the information in the DNA is replicated each time the cell divides. The amount of DNA packed into all of an adult’s cells is on the order of 100 trillion feet (about 19 billion miles)—so that if the DNA chain was stretched out, it would be long enough to reach back and forth between the Earth and the Sun more than 200 times.
3. Ooops! Mistakes will happen.
Like any biochemical process, DNA replication is inherently prone to error. Some of the most common flubs happen when the same base is replicated several times in a row. For example, if there are many Ts in succession, the enzyme that builds new DNA molecules may accidentally drop or add a base. This kind of error is called a frameshift, and if not properly repaired it can have serious consequences; for example, frameshifts are implicated in cystic fibrosis and Tay-Sachs disease. However, polymerase error is only one source of mutation. It’s hard to put a firm number on mutation rates, because they can vary by gene, by cell type, and by person.
4. Light can harm it, light can fix it.
Damage to DNA can be brought on by a variety of factors, including ionizing radiation, such as that in X-rays, chemicals in tobacco smoke and ultraviolet (UV) radiation from sunlight. UV light in particular can cause adjacent bases on the same side of the DNA chain to stick together in an off-kilter pairing called a dimer, causing a kink in the DNA chain and halting replication. Many creatures, ranging from single-celled bacteria and some types of yeast to a variety of plants and insects, can self-repair UV-caused dimers through a process called photoreactivation, also known as light repair. Photoreactivation uses energy from visible light to directly break apart the dimers. Humans and most other mammals, however, do not have the necessary enzymes to perform this sort of direct DNA repair. One mammal that does use photoreactivation in response to UV damage is the South American gray short-tailed opossum 
. (Bonus fact: This little opossum was the first marsupial to have its genome sequenced.)
5. Cut and paste to get it right.
Fortunately, all organisms have ways to fix DNA damage that do not require sunlight, collectively referred to as dark repair. One method, base excision repair, kicks in when a single strand of the DNA helix is damaged. It involves a series of enzymes that first identifies the damaged or incorrectly placed base or nucleotide and then snips out the wrong bit and pastes in the correct base or nucleotide.
A second kind of genomic repair method, nucleotide excision repair, uses a different set of enzymes to swap out long stretches of DNA. This repair process is particularly important to correct UV-caused damage. People with certain inherited mutations in nucleotide excision repair enzymes are highly susceptible to skin cancers from sun exposure.
A third repair mechanism corrects “mismatch errors” that occur when, for example, an A is matched with a C instead of the correct T. Mismatch repair is critical to correcting errors that arise when DNA is in the process of copying itself. Although scientists have not yet determined the full details of the human mismatch repair system, they estimate the process catches all but one out of every 1,000 or so mismatch errors.
In 2015, the Nobel Prize in chemistry was shared by NIGMS grantees Paul Modrich and Aziz Sancar, along with Tomas Lindahl, for their contributions toward understanding how these forms of DNA repair work.
6. There are many things we don’t know about DNA.
The DNA molecule was first isolated—from pus on discarded surgical bandages—in 1869 by the Swiss scientist Freidrich Miescher. Although researchers have learned a lot in the last 148 years about DNA’s structure and activity, much uncharted territory remains.
Take so-called junk DNA, which was estimated to account for 99 percent of DNA in the human genome. For years, this term was used to describe DNA that does not encode instructions for making proteins. Over the past several years, scientists have dropped the term as they’ve learned more about a big chunk of noncoding DNA that plays key roles in directing and regulating gene activity.
New technologies, including a suite of imaging tools collectively termed super-resolution microscopy, are allowing scientists to see cell contents and components (including DNA) at levels of resolution not available with light microscopy. The techniques are sure to bring new details about this foundational molecule into view. Still, there will always be further mysteries to probe.
No knowledgeable scientist ever thought that all noncoding DNA was junk. Please stop spreading this false history.
Today’s knowledgeable scientists have not dropped the term “junk DNA.” The consensus among those experts is that 90% of our genome is junk.
The average number of mutations per cell generation is less than one and not 100 as stated in the article.
Thanks for pointing out that our description of mutation rates and replication errors was unclear. Although the main form of DNA polymerase makes an uncorrected error slightly less often than once per cell per generation, polymerase error is only one source of mutation.
At the University of Southern California researchers team: “DNA repair: Do not call it junk” do not describe it as scrap
In a quest to develop Crysis technology; a new discovery about the mechanism of cell repair for its acid!
In a bid to develop CRISPR-Cas9, a team from the University of Southern California in the United States studied the cell’s reaction to damage to its DNA and how to repair it.
The process was carried out on mice, fruit flies and on a part of the DNA called heterochromatin, which is characterized by a highly circumvented band, encased in duplicate sequences of DNA, and was known for a short time as a “scrap”.
The researchers observed that the cell responded very quickly and strongly to a fracture that happened in this heterozygous DNA tape as if it had entered an emergency.
On the basis of previous research, it was known that the broken DNA is withdrawn to specific sites of the nucleus called nucleic pores, which are complex proteins in the membrane of the nucleus; but the mechanism of transport was not known which is discovered in this study
Where the researchers noticed that the cell formed the bridges of a specific protein called actin between the ends of the broken tape and nuclear pores and then comes another protein characterized by its ability to move and called Myosin, which pulls DNA broken along the thread of actin to reach the pores to begin the repair process.
The research has shown that the chromatin of the variant is subject to so-called ectopic recombination and where the repair is inconsistent, causing several problems,
However, this process of transport, which preceded the actual reform process, led to the reform being “safe” as described in the paper
The research demonstrated the pivotal role of actin and meosin in the process of DNA transformation and safe repair and that any defect in this system will lead to problems in the process of repair and cell imbalance
It is interesting that the news published by the university’s website on the research contains several sections, each of which started with a specific title. One of these titles, “Do not call it junk,” started with the fact that the duplicate sequences of DNA were called ” Bad “and” junk “in the last 20 years but since then have emerged important functions as well as diseases that may cause if the failure to correct correctly
From that we published a while ago about the gene “Scrap”, which turned out to be controlled by determining the sex of the fetus alone!