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Line-1 Elements: Analysis by Fluorescence In-Situ Hybridization and Nucleotide Sequences

dc.contributor.authorWaters, Paul
dc.contributor.authorDobigny, Gauthier
dc.contributor.authorWaddell, Peter J
dc.contributor.authorRobinson, Terence J
dc.date.accessioned2015-12-10T22:57:00Z
dc.date.issued2008
dc.date.updated2015-12-10T07:57:55Z
dc.description.abstractLong-interspersed nuclear element-1 (LINE-1) is a non-terminal repeat transposon that constitutes a major component of the mammalian genome. LINE-1 has a dynamic evolutionary history characterized by the rise, fall, and replacement of subfamilies. The distribution of LINE-1 elements can be viewed from a chromosomal perspective using fluorescence in-situ hybridization (FISH), as well as at the sequence level. We have designed LINE-1 primers from regions conserved among mouse, rat, rabbit, and human L1, which were able to amplify part of ORF2 from all eutherian (placental) mammals tested thus far. The product generated can be used as a FISH painting probe to examine the genomic distribution of L1 in different species. It can also be cloned and sequenced for phylogenetic analysis. Although FISH patterns resulting from LINE-1 chromosome painting and bioinformatic analyses have shown that this element accumulates in AT-rich regions of the genomes of mouse and human, our PCR amplified LINE-1 probe suggests that this is not a universal phenomenon, and that the patterns displayed in laurasiatherian, afrotherian and xenarthran species are less prominent. The "banding" like distribution of LINE-1 observed in human and mouse, therefore, appears to reflect aspects of genome architecture unique to Euarchontoglires (Supraprimates), the superordinal clade to which they belong.By sequencing the cloned amplicons used for FISH experiments and supplementing these with L1 sequences obtained from public databases, analysis by parsimony, distance-based, maximum likelihood, and "hierarchical Bayesian" or "marginal likelihood" methods provides a powerful adjunct to the FISH data. Using this approach, relatively intact LINE-1 from most placental orders tend to reflect accepted eutherian evolutionary relationships. This suggests that there were often only closely related copies active near branch points in the tree, that inactive copies tended to become extinct quite readily, and that for many orders recently active copies belong to a single lineage of this LINE.
dc.identifier.isbn9781588297648
dc.identifier.urihttp://hdl.handle.net/1885/60467
dc.publisherHumana Press Inc.
dc.relation.ispartofMethods in Molecular Biology: Phylogenomics
dc.subjectKeywords: animal; article; chromosome banding pattern; DNA sequence; fluorescence in situ hybridization; genetics; human; lagomorph; long interspersed repeat; methodology; molecular cloning; nucleotide sequence; phylogeny; polymerase chain reaction; Animals; Base S
dc.titleLine-1 Elements: Analysis by Fluorescence In-Situ Hybridization and Nucleotide Sequences
dc.typeBook chapter
local.bibliographicCitation.lastpage237
local.bibliographicCitation.placeofpublicationUSA
local.bibliographicCitation.startpage227
local.contributor.affiliationWaters, Paul, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationDobigny, Gauthier, University of Stellenbosch
local.contributor.affiliationWaddell, Peter J, University of South Carolina
local.contributor.affiliationRobinson, Terence J, University of Stellenbosch
local.contributor.authoruidWaters, Paul, u4025262
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor060408 - Genomics
local.identifier.ariespublicationu9204316xPUB541
local.identifier.scopusID2-s2.0-48849116998
local.type.statusPublished Version

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