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[[Image:DNA splicing introns off to make proteins.jpg|thumb|right|alt=Diagram showing how DNA is translated into proteins by splicing off introns.|When DNA makes a protein, introns are spliced off during this process, so only the exons remain.]] | |||
An '''intron''' is the '''''int'''''ervening, non-coding sequence of [[nucleic acid]] that is between the '''''ex'''''pressed sequences ([[exon]]s) in a [[gene]]. It is removed from the primary [[RNA]] transcript by [[RNA splicing|splicing]] and is a common feature of [[eucaryote|eucaryotic]] genes. Introns are the spacer regions of DNA that separate the information-coding parts of a gene.<ref name=twsMAR02p>{{cite news | An '''intron''' is the '''''int'''''ervening, non-coding sequence of [[nucleic acid]] that is between the '''''ex'''''pressed sequences ([[exon]]s) in a [[gene]]. It is removed from the primary [[RNA]] transcript by [[RNA splicing|splicing]] and is a common feature of [[eucaryote|eucaryotic]] genes. Introns are the spacer regions of DNA that separate the information-coding parts of a gene.<ref name=twsMAR02p>{{cite news | ||
|author= Nicholas Wade | |author= Nicholas Wade |
Revision as of 09:23, 5 March 2010
Temporary file: Intron; (possible suggestions for new material March 5, 2010)
An intron is the intervening, non-coding sequence of nucleic acid that is between the expressed sequences (exons) in a gene. It is removed from the primary RNA transcript by splicing and is a common feature of eucaryotic genes. Introns are the spacer regions of DNA that separate the information-coding parts of a gene.[1]
Generally introns are found in the DNA of more advanced species. Scientists believe that the only living creatures on earth billions of years ago were bacteria which belonged to a group called prokaryotes.[2] But about two billion years ago, a group branched off from prokaryotes called eukaryotes which evolved into much more complex organisms including animals, plants, fungi, and some protozoans, and which had bigger and more complex DNA.[2] A New York Times science reporter explains:
‘ | The eukaryote genome is downright baroque. It is typically much bigger and carries many more genes. Eukaryotes can do more with their genes, too. They can switch genes on and off in complex patterns to control where and when they make proteins. And they can make many proteins from a single gene.[2] | ’ |
Why is the DNA more advanced? It's segmented. The DNA alternates between what are called exons and introns. This allows human cells to "edit out introns" when copying genes to build proteins, and lets cells make a wide variety of different proteins from the same gene.[2] It is believed that the exons were functionless stretches whose only purpose was to break up stretches of exons, but this view has been questioned.[2] Scientist Michael Lynch suspected the addition of introns into DNA was a harmful accident at first. When an intron was wedged into the middle of a gene, cells had to be able to recognize the boundaries and "skip over" the introns when making a protein.[2] Lynch hypothesized that this first led to defective proteins, but that the overall effect of interspersed introns was a phenomenon called genetic drift which ultimately helped evolution, since it created new opportunities for adaptations to be successful.[2]
There is no single mechanism for splicing an intron from the primary RNA transcript. Introns are classified into four groups based on the mechanism of splicing. In general splicing can be either autocatalytic or be catalyzed by a large complex of proteins know as the spliceosome. Splicing can also be viewed as a form of gene regulation since alternative splicing can result in different combinations of exons in the mature RNA transcript. In this way one gene can code for distinct open reading frames and hence has the potential to code for more than one protein.
The human DNA helix, if unraveled, would be about three feet long, and the sections of introns inside it have been referred to as "mostly chaotic" and an "indecipherable wilderness".[3]
Sometimes the DNA that codes for introns is classified as junk DNA but this is an oversimplification since introns can contain functional RNA or DNA sequences; these include transfer RNA (tRNA) or microRNA (miRNA) sequences. In the chromosome, DNA sequences that code for an intron can also include enhancers that are important for gene expression.
The true role of introns is unclear but one hypothesis is that introns allow gene shuffling to occur, resulting in the creation of new exon combinations and novel proteins. The presence of an intron can also enhance gene expression since the process of RNA splicing seems to facilitate the trafficking of the mRNA out of the eucaryotic nucleus.
Discoveries
After completing the human genome in 2001, scientists found 22,000 genes, but noticed there were more than 100,000 different proteins. If each gene could make only one protein, then how could there be so many different proteins? A Washington Post reporter explained:
‘ | When a gene is activated, it is first transcribed into an intermediate molecule called mRNA. The introns are clipped out and the exons spliced together, and the whole thing is then translated into the protein. Biologists used to think one gene produced one protein. Now it's clear that one gene can produce many different proteins. Under certain conditions, a cell clips out not only the intron fillers but also one or more of the exons. This is like taking a speech and removing many of the sentences. Done in different ways, it can produce many different messages.[4] | ’ |
Scientists think that about five percent of the human genome has a "message" of one sort or another, with a particular order of nucleotide letters (A, G, C, T) being of utmost importance in determining important aspects of a human's body chemistry. Any addition, deletion, or change can have a big effect, including death.[4] Still, there are large stretches of genes which had been thought to have been "junk DNA" but is turning out to have an important role. These conserved "non-coding elements" include insulators, micro-RNAs, exon-splicing enhancers, e'-untranslated hairpins and other molecules which are "emerging from the shadows."[4] They regulate the activity of genes that do make the proteins by turning them on and off, tweaking them, and coordinating the sequential action of their effects.[4] And how these processes operate are important not only for geneticists, but for scientists who study evolution, since "more of evolution's survival-of-the-fittest battles occurred in writing the instruction manual for running the genes than in designing the genes themselves," according to a Washington Post report in 2007.[4]
The naming of intron
The names intron and exon were described as "less catchy" but nevertheless "novel" names, and the naming was against a trend of using "dull and pedantic" impenetrable Latin names.[5] In 1977, three scientists at a cafeteria in Basel, Switzerland, discussed possible names. Dr. Walter Gilbert was credited for thinking up the name intron, while Dr. Melvin Cohn coined the term exon, although he was originally thinking of the large oil firm Exxon. Dr. Cohn explained:
‘ | I was actually thinking of 'exxon' with two x's like the oil company -- it was a joke -- I was making fun of Gilbert because I didn't think those were the best possible terms. They were too slangy and didn't best describe what was going on.[5] | ’ |
Nevertheless, Dr. Gilbert wrote down the terms on a napkin, and both terms appeared in a 1978 commentary in the journal Nature.[5]
Recent research involving introns
According to one source, scientists are exploring ways of using data from introns when doing DNA analysis regarding police investigations. While each intron seems chaotic, there are repetitive sequences of the genetic alphabet sometimes called "stutters" or "burps" which can be analyzed.[3] When multiple probes are used, it's possible to analyze introns in the DNA to identify its uniqueness and produce an identification "as reliable as a human fingerprint."[3]
Scientists discovered that two DNA units that switch off the lactase gene are in "the 9th and 13th introns of a neighboring gene whose role strangely has nothing to do with lactose metabolism."[1] Scientists are discovering that the spacer-regions in DNA called introns "play unexpected roles in gene control."[1]
Researchers are studying the relationship between introns and gender-related differences in colon cancer.[6]
There are suggestions that the composition of a specific intron, a three-SNP haplotype in the intron 1 of OCA2, is related to "human eye color variation", and scientists believe two major genes and several minor ones which account for the "tremendous variation in human eye color."[7]
There was speculation that introns inside the dysbindin gene may have a role in schizophrenia.[8]
References
- ↑ 1.0 1.1 1.2 Nicholas Wade. As Scientists Pinpoint the Genetic Reason for Lactose Intolerance, Unknowns Remain, The New York Times, January 14, 2002. Retrieved on 2010-03-02. “The authors of the new report say the two DNA units that switch off the lactase gene are in the 9th and 13th introns in a neighboring gene whose role strangely has nothing to do with lactose metabolism. Introns are the spacer regions of DNA that separate the information-coding parts of a gene. Because the cell cuts out and discards the introns when a gene is activated, these disposable pieces of DNA have long been ignored. Now it seems they play unexpected roles in gene control.”
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 Carl Zimmer. From Bacteria to Us: What Went Right When Humans Started to Evolve?, The New York Times, January 3, 2006. Retrieved on 2010-03-02. “Eukaryotes can do more with their genes, too. They can switch genes on and off in complex patterns to control where and when they make proteins. And they can make many proteins from a single gene. That is because eukaryote genes are segmented into what are called exons. Exons are interspersed with functionless stretches of DNA known as introns. Human cells edit out the introns when they copy a gene for use in building a protein. But a key ability is that they can also edit out exons, meaning that they can make different proteins from the same gene. This versatility means that eukaryotes can build different kinds of cells, tissues and organs, without which humans would look like bacteria.”
- ↑ 3.0 3.1 3.2 DNA Evidence, The New York Times, June 18, 2009. Retrieved on 2010-03-02. “DNA probe analysis grew out of basic genetic research, with far different aims. A kind of serendipitous gift to police science, it takes advantage of a peculiarity within the human genetic code. Along the three feet of the double helix in each complete DNA molecule there exists, in addition to the tens of thousands of protein-coding genes, a so-far indecipherable wilderness called the intron. The intron, although it seems mostly chaotic, nevertheless contains certain repetitive sequences of the genetic alphabet, which geneticists sometimes call "stutters" or "burps."”
- ↑ 4.0 4.1 4.2 4.3 4.4 David Brown. How Science Is Rewriting the Book on Genes, Washington Post, November 12, 2007. Retrieved on 2010-03-03.
- ↑ 5.0 5.1 5.2 Stephen S. Hall. Scientists Find Catchy Names Help Ideas Fly, The New York Times, October 20, 1992. Retrieved on 2010-03-02. “Novel though less catchy are the terms "intron" and "exon," used to distinguish different regions of the genetic material. It used to be thought that a stretch of DNA forming a gene was simply copied onto a strand of RNA, which directed synthesis of a protein.”
- ↑ Reuters Health. Gene effect on colon cancer differs by gender, Reuters, April 15, 2008. Retrieved on 2010-03-02. “The research team at the Keck School of Medicine in Los Angeles, headed by Dr. Heinz-Josef Lenz, studied two variant forms of EGFR. One of the variants involved a change at a spot called codon 497 and the other involved a change in an area known as intron 1.”
- ↑ April Holladay. Hazel is in the eye of the beholder; more on memory, USA Today, 2007-03-19. Retrieved on 2010-03-02. “D.L. Duffy, G.W. Montgomery, W. Chen, Z.Z. Zhao, L. Le, M.R. James, N.K. Hayward, N.G. Martin, R.A. Sturm. A three-SNP haplotype in the intron 1 of OCA2 explains most human eye color variation. American Journal of Human Genetics, 80: 241-252 (2007).”
- ↑ Nicholas Wade. Schizophrenia May Be Tied To 2 Genes, Research Finds, The New York Times, July 4, 2002. Retrieved on 2010-03-02. “Despite years of false leads, setbacks and unsustained claims, researchers hope they are now starting to close in on some of the genes that go awry in schizophrenia, a devastating mental disease that affects two million Americans... Dr. Straub found genetic variations in the dysbindin gene that were more common in the schizophrenic patients. Curiously, they are all in introns, the spacer regions of the DNA that lie between the working parts of the dysbindin gene. The Richmond team is not sure that any of the intron changes is the causative mutation of schizophrenia and is analyzing the working parts more closely.”