A non-LTR retroelement extinction in Spermophilus tridecemlineatus

The typical mammalian genome is dominated by two types of transposable elements (TEs), the autonomous and non-autonomous non-LTR retrotransposons, i.e. LINEs and SINEs, and with few exceptions there is a sole active LINE family (L1). During an ongoing investigation of TEs in rodents we determined th...

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Veröffentlicht in:Gene 2012-05, Vol.500 (1), p.47-53
Hauptverfasser: Platt II, Roy N., Ray, David A.
Format: Artikel
Sprache:eng
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Zusammenfassung:The typical mammalian genome is dominated by two types of transposable elements (TEs), the autonomous and non-autonomous non-LTR retrotransposons, i.e. LINEs and SINEs, and with few exceptions there is a sole active LINE family (L1). During an ongoing investigation of TEs in rodents we determined that overall transposon activity has been steadily declining in Spermophilus tridecemlineatus. More specifically, the typically ubiquitous L1 activity of mammals has decreased drastically within the last 26MY. Indeed, only three L1 insertions with intact ORF1 sequences were readily identifiable and no intact ORF2 sequences were identified. The last L1 and SINE insertions date to ~5.3MYA and 4MYA, respectively. Based on our inability to computationally identify recently inserted L1 elements we suggest that S. tridecemlineatus is experiencing a quiescence or extinction of non-LTR retrotransposon activity. Such a finding represents only the fourth instance of a loss of non-LTR retrotransposon activity identified in mammals and, as such, represents an important additional data point to guide our understanding of LINE dynamics in eutherians. ► The genome of Spermophilus tridecemlineatus was queried for L1 and SINE activities. ► We were unable to identify any L1 insertions with intact ORFs 1 and 2. ► Genetic distance analysis suggest that a reduction in L1 activity began 19–26MYA ► We estimate that no LINE or SINE insertions have occurred within the last 4–5MY. ► L1 may have gone extinct in Spermophilus tridecemlineatus.
ISSN:0378-1119
1879-0038
DOI:10.1016/j.gene.2012.03.051