2000
DOI: 10.1101/gr.10.2.174
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Multiple LTR-Retrotransposon Families in the Asexual Yeast Candida albicans

Abstract: We have begun a characterization of the long terminal repeat (LTR) retrotransposons in the asexual yeast Candida albicans. A database of assembled C. albicans genomic sequence at Stanford University, which represents 14.9 Mb of the 16-Mb haploid genome, was screened and >350 distinct retrotransposon insertions were identified. The majority of these insertions represent previously unrecognized retrotransposons. The various elements were classified into 34 distinct families, each family being similar, in terms o… Show more

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Cited by 80 publications
(95 citation statements)
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“…Most of these elements appear truncated and/or rearranged, and the long terminal repeats (LTRs), typical of retroelements, often lie apart as "solo LTRs" 16,17 . Several non-LTR retrotransposons, similar to other fungal long interdispersed nuclear elements (LINEs)-like retroelements, were also identified.…”
Section: A R T I C L E Smentioning
confidence: 99%
“…Most of these elements appear truncated and/or rearranged, and the long terminal repeats (LTRs), typical of retroelements, often lie apart as "solo LTRs" 16,17 . Several non-LTR retrotransposons, similar to other fungal long interdispersed nuclear elements (LINEs)-like retroelements, were also identified.…”
Section: A R T I C L E Smentioning
confidence: 99%
“…In general, the C. elegans genome appears to have a relatively low tolerance for LTR retrotransposons (<1%). Whereas we have identified 124 full-length, fragmented, or solo LTR Cer elements in the sequenced (N2) C. elegans genome, >350 LTR retrotransposon elements have been described in the yeast Candida albicans (Goodwin and Poulter 2000) and >300 in Saccharomyces cerevisiae (Kim et al 1998), both species with genomes nearly an order of magnitude smaller than C. elegans (C. elegans Sequencing Consortium 1998).…”
Section: Discussion the C Elegans Genome Contains Relatively Few Fammentioning
confidence: 99%
“…Sequencing was performed using an ABI377 DNA sequencer at the University of Otago. Southern blots were performed as described previously (Goodwin & Poulter, 2000). Autoradiographs were scanned using a Bio-Rad GS-800 Calibrated Densitometer and Quantity One software.…”
Section: Methodsmentioning
confidence: 99%