Abstract:Abstract.Gene movement by the newly-described Helitron family of transposable elements apparently has significantly impacted the evolution of this genome and has contributed to the lack of intra-specific gene collinearity between different maize inbred lines. The abundance of these elements and the extent of diversity among them remain largely undetermined. Several hypotheses have been proposed to explain their transposition and mechanism by which these elements prolifically capture and mobilize gene sequences… Show more
“…These termini have been used to search for other family members in the maize genome database (Gupta et al 2005;Lal et al 2008). Using similar methodologies, we discovered a 50bp region spanning positions 1161-1211 of a genomic clone (gi: 21842135) that was nearly identical to the 5 0 termini of the Helitron insertions in sh2-7527 and ba1-ref (Lal et al 2003;Gupta et al 2005).…”
Section: Maize Cyp72a27-zm Represents a Cytochrome P450 Monooxygenasementioning
confidence: 98%
“…The clones displaying both termini of either mutant insertion were further perused for Helitrons (Lal et al, 2008). The intervening sequence between the termini was considered a Helitron insertion.…”
The mass movement of gene sequences by Helitrons has significantly contributed to the lack of gene collinearity reported between different maize inbred lines. However, Helitron captured-genes reported to date represent truncated versions of their progenitor genes. In this report, we provide evidence that maize CYP72A27-Zm gene represents a cytochrome P450 monooxygenase (P450) gene recently captured by a Helitron and transposed into an Opie-2 retroposon. The four exons of the CYP72A27 gene contained within the element contain a putative open reading frame (ORF) for 428 amino acid residues. We provide evidence that Helitron captured CYP72A27-Zm is transcribed. To identify the progenitor gene and the evolutionary time of capture, we searched the plant genome database and discovered other closely related CYP72A27-Zm genes in maize and grasses. Our analysis indicates that CYP72A27-Zm represents an almost complete copy of maize CYP72A26-Zm gene captured by a Helitron about 3.1 million years ago (mya). The Helitron-captured gene then duplicated twice, approximately 1.5-1.6 mya giving rise to CYP72A36-Zm and CYP72A37-Zm. These data provide evidence that Helitrons can capture and mobilize intact genes that are transcribed and potentially encode biologically relevant proteins.
“…These termini have been used to search for other family members in the maize genome database (Gupta et al 2005;Lal et al 2008). Using similar methodologies, we discovered a 50bp region spanning positions 1161-1211 of a genomic clone (gi: 21842135) that was nearly identical to the 5 0 termini of the Helitron insertions in sh2-7527 and ba1-ref (Lal et al 2003;Gupta et al 2005).…”
Section: Maize Cyp72a27-zm Represents a Cytochrome P450 Monooxygenasementioning
confidence: 98%
“…The clones displaying both termini of either mutant insertion were further perused for Helitrons (Lal et al, 2008). The intervening sequence between the termini was considered a Helitron insertion.…”
The mass movement of gene sequences by Helitrons has significantly contributed to the lack of gene collinearity reported between different maize inbred lines. However, Helitron captured-genes reported to date represent truncated versions of their progenitor genes. In this report, we provide evidence that maize CYP72A27-Zm gene represents a cytochrome P450 monooxygenase (P450) gene recently captured by a Helitron and transposed into an Opie-2 retroposon. The four exons of the CYP72A27 gene contained within the element contain a putative open reading frame (ORF) for 428 amino acid residues. We provide evidence that Helitron captured CYP72A27-Zm is transcribed. To identify the progenitor gene and the evolutionary time of capture, we searched the plant genome database and discovered other closely related CYP72A27-Zm genes in maize and grasses. Our analysis indicates that CYP72A27-Zm represents an almost complete copy of maize CYP72A26-Zm gene captured by a Helitron about 3.1 million years ago (mya). The Helitron-captured gene then duplicated twice, approximately 1.5-1.6 mya giving rise to CYP72A36-Zm and CYP72A37-Zm. These data provide evidence that Helitrons can capture and mobilize intact genes that are transcribed and potentially encode biologically relevant proteins.
“…The first examples of de novo Helitron insertions were isolated from two maize mutants (46, 73). Helitrons contribute substantially to a lack of colinearity in locus alignments across maize inbred lines (72). Gene annotation differences at the bz locus between two inbred maize lines reflect fragments captured/transduced by two Helitron transposons (124) (Figure 3 h ).…”
Section: Distribution Of Recent Transposon Activitymentioning
Transposons are DNA sequences capable of moving in genomes. Early evidence showed their accumulation in many species and suggested their continued activity in at least isolated organisms. In the past decade, with the development of various genomic technologies, it has become abundantly clear that ongoing activity is the rule rather than the exception. Active transposons of various classes are observed throughout plants and animals, including humans. They continue to create new insertions, have an enormous variety of structural and functional impact on genes and genomes, and play important roles in genome evolution. Transposon activities have been identified and measured by employing various strategies. Here, we summarize evidence of current transposon activity in various plant and animal genomes.
“…The majority of the elements identified thus far represent nonautonomous Helitrons containing chimeric segments derived from multiple genes although the analysis of the complete sequencing of one single maize inbred line provides only biased information of the extent and diversity of gene capture, transposition, and amplification by Helitrons [112]. In addition to Helitron, the Mutator superfamily possesses non-autonomous elements, called Pack-MULES, that have the ability to capture segments of nuclear gene(s) which can be arranged in chimeras [113,114]. Further, molecular evidence has revealed that these novel chimeras can be both transcribed and translated, which suggest that this mechanism of gene fragment capture inside of non-autonomous elements can produce, and evolve into, novel protein coding sequences [113,114].…”
Section: Transposons and Genetic Colinearitymentioning
confidence: 99%
“…In addition to Helitron, the Mutator superfamily possesses non-autonomous elements, called Pack-MULES, that have the ability to capture segments of nuclear gene(s) which can be arranged in chimeras [113,114]. Further, molecular evidence has revealed that these novel chimeras can be both transcribed and translated, which suggest that this mechanism of gene fragment capture inside of non-autonomous elements can produce, and evolve into, novel protein coding sequences [113,114]. Much like the Helitron elements, Pack-MULE transposition and amplification can lead to deviations in intraspecific synteny, and recent research has shown that Pack-MULEs preferentially capture GC-rich genomic segments and displayed biased insertion into the 5 end of coding regions [115].…”
Section: Transposons and Genetic Colinearitymentioning
Zea mays (maize) has historically been used as a model species for genetics, development, physiology and more recently, genome structure. The maize genome is complex with striking intraspecific variation in gene order, repetitive DNA content, and allelic content exceeding the levels observed between primate species. Maize genome complexity is primarily driven by polyploidization and explosive amplification of LTR retrotransposons, with the counteracting effect of unequal and illegitimate crossover. Transposable elements have been shown to capture genic content, create chimeras, and amplify those sequences via transposition. New sequencing platforms and hybridization-based strategies have appeared over the past decade which are being applied to maize and providing the first genome-wide comprehensive view of structural variation and will provide the basis for investigating the interplay between repeats and genes as well as the amount of species level diversity within maize.
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