Zj. Tu et al., STRUCTURAL, GENOMIC, AND PHYLOGENETIC ANALYSIS OF LIAN, A NOVEL FAMILY OF NON-LTR RETROTRANSPOSONS IN THE YELLOW-FEVER MOSQUITO, AEDES-AEGYPTI, Molecular biology and evolution, 15(7), 1998, pp. 837-853
A retrotransposon named Lian-Aa1 was discovered in an intron of an AaH
R3-1 gene of the yellow fever mosquito, Aedes aegypti. This retrotrans
poson contained a long open reading frame with 1,219 amino acids that
included endonuclease, reverse transcriptase, and RNase II domains. It
was shown that in the Rock strain of Ae. aegypti, there were up to 1,
380 copies of Lian elements, equivalent to 0.8% of the entire genome.
Five additional copies of Lian elements were isolated, mapped by restr
iction digestion, and partially sequenced. The 5' and 3' ends of the L
ian family were determined by comparing the terminal sequences of the
six copies and were subsequently confirmed by the identification of pu
tative target duplications flanking Lian-Aa1 and Lian-Aa2. The Lian fa
mily is likely a novel family of non-long-terminal-repeat (non-LTR) re
trotransposons that terminate in a repeat of (CTGATAC)(2). On average,
the six copies of Lian elements showed only 0.6% sequence divergence
at the nucleotide level in both a 735-bp region at the 5' end and a 1,
124-bp coding region. Genomic Southern blots also revealed a very high
degree of similarity among hundreds of Lian elements, suggesting very
recent activity of Lian. Furthermore, all six analyzed Lian elements
were closely associated with one or more different families of repetit
ive elements. It is possible that these associations could reflect the
complex relationship between Linn elements and the rest of the Ae. ae
gypti genome. Phylogenetic analyses based on the reverse transcriptase
, domains of 36 non-LTR retrotransposons including Lian-Aa1 identified
five major subgroups that were supported by bootstrap replications. I
n contrast to the majority of non-LTR retrotransposons, Lian-Aa1 has a
n RNase H domain that is similar to a few other non-LTR retrotransposo
ns and some retroviruses, which is consistent with the previously prop
osed independent assortment of different domains during the evolution
of retroelements.