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who discovered transposable elements

by Rubie Morar Published 3 years ago Updated 2 years ago
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Barbara McClintock

What is the history of transposable elements?

The first TEs were discovered in maize (Zea mays) by Barbara McClintock in 1948, for which she was later awarded a Nobel Prize. She noticed chromosomal insertions, deletions, and translocations caused by these elements.

When were transposons first discovered?

Barbara McClintock at her laboratory desk, 1971. By the 1970s the great strides made in molecular biology led to the discovery of transposons in other organisms, starting with viruses and bacteria. We now know that transposons constitute more than 65% of our genomes and approximately 85% of the maize genome.

What are transposable elements in biology?

Transposable Genetic Elements Transposons are small pieces of DNA (500–1500 bp long) capable of moving themselves from one place to another within a genome. These mobile genetic elements were first recognized in maize (corn), but are now known to be present in essentially all organisms.

Can transposable elements (TEs) be used to study mouse genetics?

Transposable elements (TEs) have been used to study the genetics of a wide variety of species, including prokaryotes, plants, yeast, and Drosophila. The use of TEs to study mouse genetics has previously not been possible as mice do not have endogenous, highly active TEs like other organisms.

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How was transposon discovered?

Her studies of chromosome breakage in maize led her to discover a chromosome-breaking locus that could change its position within a chromosome. McClintock went on to discover other such mobile elements, now known as transposons.

Who discovered transposable genes?

scientist Barbara McClintockTransposons were first discovered in corn (maize) during the 1940s and '50s by American scientist Barbara McClintock, whose work won her the Nobel Prize for Physiology or Medicine in 1983. Since McClintock's discovery, three basic types of transposons have been identified.

Who discovered transposable elements in maize?

geneticist Barbara McClintockTransposable elements, or transposons, are DNA sequences that can move locations within a genome (“jumping genes”). Discovered in corn by Nobel-winning geneticist Barbara McClintock in the 1940s, they were long considered by many scientists to have little role in genetics.

What are the two types of transposable elements?

Transposons are mobile elements that can move about the plant (or animal) genome. There are two types of transposons, what may be termed true transposons such as the Ac/Ds and MuDR/Mu maize transposons (see Walbot, 2000; Bennetzen, 2005; Lisch, 2009 for reviews) and retrotransposons (see Chapter 2, Section I, F).

Who discovered chromosomes?

Walther FlemmingIt's generally recognized that chromosomes were first discovered by Walther Flemming in 1882.

Who discovered polytene chromosome?

BalbianiPolytene chromosomes were first discovered in the 1880s in insects (Balbiani 1881). One of the earliest published examples of polytene chromosomes is of Chironimus salivary gland chromosomes found in Walther Flemming's 1882 book, Zellsubstanz, Kern, und Zelltheilung (Flemming 1882).

Who discovered chromosomes in 1875?

"Walther Flemming: pioneer of mitosis research".

Why transposons are called jumping genes?

Transposons are a group of mobile genetic elements that are defined as a DNA sequence. Transposons can jump into different places of the genome; for this reason, they are called jumping genes.

What are transposons and its types?

Transposons themselves are of two types according to their mechanism, which can be either "copy and paste" (class I) or "cut and paste" (class II). Class I (Retrotransposons, aka retoposons): They copy themselves in two stages, first from DNA to RNA by transcription, then from RNA back to DNA by reverse transcription.

Where are transposons found?

DNA transposons have been found in both prokaryotic and eukaryotic organisms. They can make up a significant portion of an organism's genome, particularly in eukaryotes.

What means allele?

An allele is one of two or more versions of DNA sequence (a single base or a segment of bases) at a given genomic location. An individual inherits two alleles, one from each parent, for any given genomic location where such variation exists. If the two alleles are the same, the individual is homozygous for that allele.

What is the purpose of transposons?

Transposons are repetitive DNA sequences that have the capability to move (transpose) from one location to another in genome. Transposon movement can result in mutations, alter gene expression, induce chromosome rearrangements and, due to increase in copy numbers, enlarge genome sizes.

What did Creighton and McClintock discover?

By 1932, McClintock had published nine articles on maize chromosomes, including studies of the centromere and the nucleolus, and a landmark 1931 PNAS article in which she and graduate student Harriet Creighton demonstrated genetic crossing-over at the chromosomal level and showed that genetic recombination involved the ...

When did Barbara McClintock Discover genes?

1944Barbara McClintock discovers that genes can jump around on chromosomes, showing that the genome is more dynamic than previously thought.

Why transposons are called jumping genes?

Transposons are a group of mobile genetic elements that are defined as a DNA sequence. Transposons can jump into different places of the genome; for this reason, they are called jumping genes.

What is a transposable element?

Transposable elements (TE) or transposons can be defined as small, mobile DNA sequences that move around chromosomes with no regard for homology, and insertion of these elements may produce deletions, inversions, chromosomal fusions, and even more complicated rearrangements. Transposons are mobile genetic elements that often carry an antimicrobial ...

What are the characteristics of transposable elements?

Some salient features of transposable elements are: These are the DNA sequences that code for enzymes which result in self-duplication and insertion into a new DNA site. Transposons are involved in transposition events which include both recombination and replication, which usually generates two copies ...

What are transposons involved in?

Transposons are involved in transposition events which include both recombination and replication, which usually generates two copies of the original transposable elements. One of the copies remains at the parent site, whereas the other one reaches the target site on the host chromosome.

Why do transposons carry genes?

Because transposons carry the genes for initiation of RNA synthesis, some previously dormant genes might be activated. A transposable element doesn’t have a site for the origin of replication. As a result, it cannot replicate without the host chromosome as plasmids or phages.

What happens when a transposable gene is inserted into a functional gene?

A transposable gene, when inserted into a functional gene, might disable the gene. Multiple copies of the same sequence hinder the chromosome pairing during cell division resulting in chromosome duplication. Expression of harmful disease-causing proteins in the transposons affects the normal cellular function.

What is a short sequence in a transposon?

A short (less than ten b.p.) sequence is present on either side of a transposon. The insertion of transposon causes duplication of a singular target sequence, which then appear as direct repeats flanking the inserted transposable element. The flanking direct repeats are not considered part of the transposon.

How do transposable elements move from one bacterium to another?

These elements can insert randomly, move from plasmids to the chromosome, and vice versa, and can be moved from one bacterium to another by conjugation, transformation, or transduction. Transposable elements make up a significant fraction of the genome and are responsible for much of the mass of DNA in a eukaryotic cell.

When did TEs fade?

Except for their use as potential genetic tools, the interest in molecular analyses of TEs faded between 1990 and 2000, and the population approach was not really understood. Researchers were interested in the precise mechanisms by which TE activity and copy number are regulated, rather than in global processes such as those involved at the level of populations. Some forces do indeed select against TE insertions (due to the deleterious impact of insertions or of their effects through ectopic recombination), and drift, resulting from the small effective population size of the host, may be at work even for TEs that are strongly regulated at the molecular level. However, there was a great renewal of interest when sequenced genomes of organisms such as humans, mice, and plants became available. The large amount of TEs present in these organisms forced us to finally reconsider the assumption that the TEs were purely selfish and to envisage instead that they (or some of their insertions) may have evolved toward genomic functions (they are said to have been “domesticated”) ( McDonald 1983 ). This idea of a possible genomic function of some TE insertions was initially rejected, mostly because no fixed TE insertions had been identified in chromosomes. However, this was mainly due to the in situ hybridization technique used, which tended to detect large insertions rather than smaller ones, such as the solo LTRs of retrotransposons that were later shown to be associated with gene regulation. In addition to the accepted notion that specific TE domestication has led to the RAG genes of the immunoglobulin system, which are derived from DNA transposons and act like a transposase in the V (D)J recombination system ( Kapitonov and Jurka 2005 ), and the use of the TART and HeT elements as protectors of telomeres in Drosophila ( Pardue and Debaryshe 2003) instead of the classical sequences usually found in many organisms, or the acquisition of novel cellular functions by recruitment of TE-derived coding sections ( Miller et al. 1999 ), the TEs were also seen as responsible for gene regulation.

How did genetic factors influence evolution?

The idea that some genetic factors are able to move around chromosomes emerged more than 60 years ago when Barbara McClintock first suggested that such elements existed and had a major role in controlling gene expression and that they also have had a major influence in reshaping genomes in evolution. It was many years, however, before the accumulation of data and theories showed that this latter revolutionary idea was correct although, understandably, it fell far short of our present view of the significant influence of what are now known as “transposable elements” in evolution. In this article, I summarize the main events that influenced my thinking about transposable elements as a young scientist and the influence and role of these specific genomic elements in evolution over subsequent years. Today, we recognize that the findings about genomic changes affected by transposable elements have considerably altered our view of the ways in which genomes evolve and work.

When were transposons first discovered?

Transposons were first discovered in corn (maize) during the 1940s and ’50s by American scientist Barbara McClintock, whose work won her the Nobel Prize for Physiology or Medicine in 1983. Since McClintock’s discovery, three basic types of transposons have been identified.

Why are transposons considered junk DNA?

They have long been referred to as “junk” DNA because they appear to serve little or no purpose or as “selfish” DNA because they serve only to copy and amplify themselves within genomes. In rare cases, however, transposons are associated with genetic mutations or chromosomal rearrangements that cause disease in humans.

What is the first step in retrotransposition?

The first step in retrotransposition occurs when the transposable DNA is copied into RNA. The RNA segment then jumps to another location in the genome. However, in order to be inserted into the genome at the new site, the RNA must be copied back into DNA by an enzyme called reverse transcriptase.

How do class II elements move?

Class II elements are simply segments of DNA that move from one place to another via a “cut and paste” mechanism. Most, if not all, of these elements encode an enzyme called transposase, which acts to cleave the ends of the transposon, freeing it from its initial location in the genome. Transposase also cleaves target sites where the element is to be inserted. Once the transposon is ligated (bound) into its new position, gaps that are left in the DNA sequence are filled in through the synthesis of nucleotides. Class II transposons range in length from 1,000 to as many as 40,000 base pairs.

What is the function of retrotransposons?

Retrotransposons function by a “copy and paste” mechanism.

How many base pairs are in a class II transposon?

Class II transposons range in length from 1,000 to as many as 40,000 base pairs.

What is jumping gene?

Alternative Titles: jumping gene, transposable element. Transposon, class of genetic elements that can “jump” to different locations within a genome. Although these elements are frequently called “jumping genes,” they are always maintained in an integrated site in the genome. In addition, most transposons eventually become inactive ...

Types of Transposons

Today, scientists know that there are many different types of TEs, as well as a number of ways to categorize them. One of the more common divisions is between those TEs that require reverse transcription (i.e., the transcription of RNA into DNA) in order to transpose and those that do not.

What Jumping Genes Do (Besides Jump)

The fact that roughly half of the human genome is made up of TEs, with a significant portion of them being L1 and Alu retrotransposons, raises an important question: What do all these jumping genes do, besides jump? Much of what a transposon does depends on where it lands.

Transposons Are Not Always Destructive

Not all transposon jumping results in deleterious effects. In fact, transposons can drive the evolution of genomes by facilitating the translocation of genomic sequences, the shuffling of exons, and the repair of double-stranded breaks. Insertions and transposition can also alter gene regulatory regions and phenotypes.

References and Recommended Reading

Bailey, J. A., et al. Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis. Proceedings of the National Academy of Sciences 97, 6634–6639 (2000)

What are transposable elements?

Transposable elements (TEs) are selfish elements that proliferate in genomes and contribute significantly to the evolution of genome architecture. Over the past two decades, genome sequencing has revealed complex dynamics of TE proliferation across species. A key question in genome evolution is: What determines variation in TE proliferation across species? Population genetic models that assume most TE insertions are harmful and also at equilibrium can explain many patterns of TE activity across species and within genomes. However, as population sequencing becomes common, there is a need for additional models that consider the role of host TE regulation and mating system.

What is the function of transposable elements in a transposon?

Transposable elements of the composite transposon class have the capacity to generate adjacent deletions. In this section, I describe the use of this property to study the essentiality of genes (or groups of genes). In a subsequent section, I describe how composite transposon deletion generation can be used to generate nested families of protein deletions.

How many types of transposons are there?

Composite transposons can give rise to four types of transposons. Composite transposons such as Tn5 contain two identical or nearly identical insertion sequences (IS50L and IS50R in the case of Tn5) that bracket additional genes. Depending on which end recognition (ER) sequences are chosen by the transposase during synapsis, ...

What is transposon domestication?

Transposon Domestication. Some transposons have contributed to the creation of new genes, in a process described as ‘domestication’. This occurs when proteins or protein domains encoded by TEs become co-opted into functional host proteins.

What are transposons in DNA?

Transposable Genetic Elements. Transposons are small pieces of DNA (500–1500 bp long) capable of moving themselves from one place to another within a genome. These mobile genetic elements were first recognized in maize (corn), but are now known to be present in essentially all organisms.

Why do transposons have repetitive DNA sequences?

Transposons usually have repetitive DNA sequences at each end to facilitate their excision from the genome, and include a gene for the enzyme (transposase) that catalyzes excision. Once excised, transposons reenter the genome at random positions and usually do not disrupt the general architecture of the genome.

What is the P element in drosophila?

The P element of Drosophila encodes its own repressor; an alternative splice in the transposase transcript determines whether an active transposase or a repressor protein is synthesized. This alternative splice ensures that the transposon can jump in the germline, but remains silent in somatic cells.

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Transposable Elements Definition

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Transposable elements (TE) or transposons can be defined as small, mobile DNA sequences that move around chromosomes with no regard for homology, and insertion of these elements may produce deletions, inversions, chromosomal fusions, and even more complicated rearrangements. 1. Transposons are mobil…
See more on microbenotes.com

Characteristics of Transposable Elements

  • Some salient features of transposable elements are: 1. These are the DNA sequences that code for enzymes which result in self-duplication and insertion into a new DNA site. 2. Transposons are involved in transposition events which include both recombination and replication, which usually generates two copies of the original transposable elements. One of the copies remains at the pa…
See more on microbenotes.com

Types of Transposable Elements

  • Transposable elements are of the following two types: 1. The insertion sequences (IS) or simple transposons are shorter sequences (800 to 1500 bp) and do not code for proteins. 2. These sequences carry the genetic information necessary for their transposition (e., the gene for the enzyme transposase) 3. Insertion sequences have been identified in bacteriophages, in F factor …
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Examples of Transposable Elements

  1. Tn 3 transposon has 4957 bp and contains three genes such as tnp A, tnp R and
  2. Tnp Acodes for transposase having 1015 amino acids and required for transposition.
  3. Tnp Rcodes for a repressor (also called resolvase), containing 185 amino acids, which regulates the transposase.
  4. Blacodes for a β-lactamase enzyme which confers resistance to the antibiotic ampicillin.
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Applications of Transposable Elements

  1. Transposable elements can be used as a genetic tool for the analysis of gene expression and protein functioning.
  2. These are used in genetic engineering to insert or remove specific genetic sequences, and also to cause frameshift mutation.
  3. The Tc1/mariner-class of TEs Sleeping Beauty transposon system is being studied for use in …
  1. Transposable elements can be used as a genetic tool for the analysis of gene expression and protein functioning.
  2. These are used in genetic engineering to insert or remove specific genetic sequences, and also to cause frameshift mutation.
  3. The Tc1/mariner-class of TEs Sleeping Beauty transposon system is being studied for use in human gene therapy.

Negative Effects of Transposable Elements

  1. A transposable gene, when inserted into a functional gene, might disable the gene.
  2. Multiple copies of the same sequence hinder the chromosome pairing during cell division resulting in chromosome duplication.
  3. Expression of harmful disease-causing proteins in the transposons affects the normal cellular function.
See more on microbenotes.com

References

  1. Verma PS and Agarwal VK (2005). Cell Biology, Genetics, Molecular Biology, Evolution, and Ecology. Multicolored Edition.
  2. McGee, David & Coker, Christopher & Harro, Janette & Mobley, Harry. (2001). Bacterial Genetic Exchange. Doi: 10.1038/npg.els.0001416.
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Internet Sources

  1. 7% – http://www.yourarticlelibrary.com/biology/brief-notes-on-simple-transposons-complex-transposons-discussed/3852
  2. 3% – https://www.svpgcollege.org.in/transposable-genetic-elements-jumping-genes/
  3. 3% – https://studydocz.com/brief-notes-on-simple-transposons-complex-transposons-discussed-28119
  1. 7% – http://www.yourarticlelibrary.com/biology/brief-notes-on-simple-transposons-complex-transposons-discussed/3852
  2. 3% – https://www.svpgcollege.org.in/transposable-genetic-elements-jumping-genes/
  3. 3% – https://studydocz.com/brief-notes-on-simple-transposons-complex-transposons-discussed-28119
  4. 2% – https://wiki2.org/en/Transposable_element

Abstract

  • Anecdotal, Historical and Critical Commentaries on Genetics SINCE the radical suggestion by Barbara McClintock in the 1950s, based on her extensive genetic analyses in maize, that some genes might move along chromosomes, our knowledge of transposable elements (TEs) has vastly increased. TEs are no longer seen as “junk” and “selfish” pieces of DNA—t...
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Transposable Elements as Components of Genetic Diversity

  • In the 1970s, the field of population genetics was dominated by analysis of the genetic polymorphism of populations using allozymes, with the aim of deciphering population structuring (Lewontin 1974). The entire emphasis was on the role of point mutations in coding regions as the primary source of evolutionary change. Despite the observations of McClintock (1950) that in ma…
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Transposable Elements as Players in Evolution

  • Except for their use as potential genetic tools, the interest in molecular analyses of TEs faded between 1990 and 2000, and the population approach was not really understood. Researchers were interested in the precise mechanisms by which TE activity and copy number are regulated, rather than in global processes such as those involved at the level of populations. Some forces …
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Concluding Remarks

  • TEs were initially considered to be just junk DNA, with no influence on the genes and endowed solely with the capacity to invade genomes and populations because of their ability to transpose. They began to acquire their more exalted status once we recognized their influence on recombination rates and chromosomal rearrangements, their role as mutators and gene regulat…
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Acknowledgements

  • I thank my colleagues E. Lerat and C. Vieira for their helpful comments, A. S. Wilkins for his useful suggestions that greatly improved the text, and Monika Ghosh for her invaluable help with the English language during all these years.
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1.Transposable element - Wikipedia

Url:https://en.wikipedia.org/wiki/Transposable_element

31 hours ago Transposable elements were discovered by Barbara McClintock (1965) through an analysis of genetic instability in maize (corn). The instability involved chromosome breakage and was found to occur at sites where transposable elements were located.

2.Videos of Who Discovered Transposable elements

Url:/videos/search?q=who+discovered+transposable+elements&qpvt=who+discovered+transposable+elements&FORM=VDRE

13 hours ago Since McClintock’s discovery, three basic types of transposons have been identified. These include class II transposons, miniature inverted-repeat transposable elements (MITEs, or class III transposons), and retrotransposons (class I transposons).

3.The Mode of Discovery of Transposable Elements

Url:https://www.yourarticlelibrary.com/biology/the-mode-of-discovery-of-transposable-elements-biology-701-words/6455

26 hours ago Although biologists were initially skeptical of McClintock’s discovery, they now recognize that transposable elements make up a significant portion of most eukaryotic genomes.

4.Brief History of the Status of Transposable Elements: …

Url:https://academic.oup.com/genetics/article/186/4/1085/6063643

6 hours ago As previously mentioned, McClintock is best known for her discovery of transposable elements through experimentation with maize.

5.transposon | genetics | Britannica

Url:https://www.britannica.com/science/transposon

6 hours ago Abstract. Transposable elements (TEs) have been used to study the genetics of a wide variety of species, including prokaryotes, plants, yeast, and Drosophila. The use of TEs to study mouse genetics has previously not been possible as mice do not have endogenous, highly active TEs like other organisms.

6.Transposons | Learn Science at Scitable - Nature

Url:https://www.nature.com/scitable/topicpage/transposons-the-jumping-genes-518/

19 hours ago  · McClintock went on to discover other such mobile elements, now known as transposons. She also found that depending on where they inserted into a chromosome these mobile elements could reversibly alter the expression of other genes.

7.Barbara McClintock and the Discovery of Jumping …

Url:https://www.nature.com/scitable/topicpage/barbara-mcclintock-and-the-discovery-of-jumping-34083/

7 hours ago who discovered transposable elements and in what model system? ... yes; on plasmids; transposable elements on the main chromosome tend to be eliminated by selection or drift as a result of asexual reproduction. what is difference between class 1 and class 2 …

8.Transposable Element - an overview | ScienceDirect Topics

Url:https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/transposable-element

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9.Barbara McClintock and the discovery of jumping genes

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Url:https://quizlet.com/73277479/chapter-15-flash-cards/

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