Difference between revisions of "Genomic inversion"
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===Definition=== | ===Definition=== | ||
− | A genomic inversion is when a region of a genome or chromosome gets flipped in place. These usually happen at genomic regions with nearly identical sequence, implying a mechanism similar to non-homologous recombination. | + | A genomic inversion is when a region of a genome or chromosome gets flipped in place. These usually happen at genomic regions with nearly identical sequence, implying a mechanism similar to [[non-homologous recombination]]. |
===Bacteria=== | ===Bacteria=== | ||
In bacterial genomes, inversion often occur at transposon or ribosomal gene sequences, and happen symmetrically around the [[origin of replication]]. The latter causes a characteristic pattern in [[syntenic dotplots]] called an [[x alignment]]. | In bacterial genomes, inversion often occur at transposon or ribosomal gene sequences, and happen symmetrically around the [[origin of replication]]. The latter causes a characteristic pattern in [[syntenic dotplots]] called an [[x alignment]]. |
Revision as of 11:28, 18 February 2010
Definition
A genomic inversion is when a region of a genome or chromosome gets flipped in place. These usually happen at genomic regions with nearly identical sequence, implying a mechanism similar to non-homologous recombination.
Bacteria
In bacterial genomes, inversion often occur at transposon or ribosomal gene sequences, and happen symmetrically around the origin of replication. The latter causes a characteristic pattern in syntenic dotplots called an x alignment.