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Encyclopedia > Retroposon

Retrotransposons are mobile genetic elements and are ubiquitous in the genomes of many eukaryotic organisms. They are particularly abundant in plants, where they are often a principal component of nuclear DNA. In maize 50-80%, and in wheat up to 90%, of the genome is made up of retrotransposons.


Biological activity

The retrotransposons replicative mode of transposition increases the copy numbers of elements rapidly and thereby greatly increasing plant genome size. Like DNA transposable elements, they can induce mutations by inserting near or within genes. Furthermore, retrotransposon induced mutations are relatively stable; because the sequence at the insertion site is retained as they transpose via replication mechanism.


Retrotransposons copy themselves to RNA and then, via reverse transcriptase, back to DNA. Transposition and survival of retrotransposons within the host genome are possibly regulated both by retrotransposon- and host-encoded factors, to avoid deleterious effects on host and retrotransposon as well, in a relationship that has existed for many millions of years between retrotransposons and their plant hosts. The understanding how retrotransposons and their hosts’ genomes have co-evolved mechanisms to regulate transposition, insertion specificities, and mutational outcomes in order to optimize each other's survival is just in the infancy.


Types of retrotransposons

Retrotransposons belong to class I type of mobile elements, consists of two sub-types, the long terminal repeat (LTR) and the non-LTR retrotransposons. The LTR retrotransposons have direct LTRs that range from ~100 bp to over 5 kb in size. LTR retrotransposons are further sub-classified into the Ty1-copia and the Ty3-gypsy groups based on both their degree of sequence similarity and the order of encoded gene products. Ty1-copia and Ty-3 gypsy groups of retrotransposons are commonly found in high copy number (up to a few million copies per haploid nucleus) in plants with large genomes. Ty1-copia retrotransposons are abundant in species ranging from single-cell algae to bryophytes, gymnosperms, and angiosperms. Ty3-gypsy retrotransposons are also widely distributed, including both gymnosperms and angiosperms. LTR retrotransposons make up approximatey 8% of the human genome.


The non-LTR retrotransposons, consists of two sub-types, long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs). They can also be found in high copy numbers (up to 250,000) in the plant species.

  • LINES (long interspersed elements) are long DNA sequences that represent reverse-transcribed RNA molecules originally transcribed by RNA polymerase II into mRNA (messenger RNA to be translated into protein on ribosomes). Also called pseudogenes, they do not contain introns or promoters, but can code for reverse transcriptase or integrase, enabling them to copy both themselves and other, noncoding LINES. Because LINES move by copying themselves (instead of moving, like transposons do), they enlarge the genome. The human genome, for example, contains about 500,000 LINES, which is roughly 21% of the genome. LINES are used to generate genetic fingerprints.
  • SINES (short interspersed elements) are short DNA sequences that represent reverse-transcribed RNA molecules originally transcribed by RNA polymerase III into tRNA, rRNA, and other small nuclear RNAs. SINEs do not encode a functioal reverse transcriptase protein and rely on other mobile elements for transposition. The most common SINES are called Alu sequences. Alu elements are about 300 base pairs long, do not contain any coding sequences, and can be recognized by the restriction enzyme AluI (thus the name). With about 1 million copies, they make up about 11% of the human genome. Both LINES and SINES are also called "selfish DNA" or "junk DNA", because they do not serve any known purpose. SINEs make up 13.5% od the human genome.

Several viruses, like HIV-1 or HTLV-1 behave like retroposons and contain both reverse transcriptase and integrase, the retroposon equivalent of transposase.


See also


  Results from FactBites:
 
Retroposon (272 words)
Retroposons, also called retrotransposons, are related to transposons.
Many retroposons have LTRs (long terminal repeats) at their ends that can contain over 1000 base pairs each.
Several viruses, like HIV-1 or HTLV[?]-1 behave like retroposons and contain both reverse transcriptase and integrase, the retroposon equivalent of transposase[?].
Plagiarized Errors and Molecular Genetics (16141 words)
The crucial observation relating the discovery of pseudogenes and retroposons to the theory of evolution is this: some pseudogenes and retroposons are shared between different species, as though they were copied from a pseudogene or retroposon in a common ancestor.
As is the case for most mutations, the overwhelming majority of retroposon insertions occur in the non-functional DNA between genes, and have no effect on the cell or organism; and it is this vast set of insertions, shared between species, that provide the basis for the present argument supporting evolution.
This is possible because specific classes of similar retroposons are thought to have populated the mammalian genome in waves, with certain families (and subfamilies, in the case of Alu and LINE sequences) being copied from a small number of source retroposons active at any particular period in our evolutionary history.
  More results at FactBites »


 

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