F. Chavanne et al., STRUCTURE AND EVOLUTION OF CYCLOPS - A NOVEL GIANT RETROTRANSPOSON OFTHE TY3 GYPSY FAMILY HIGHLY AMPLIFIED IN PEA AND OTHER LEGUME SPECIES/, Plant molecular biology, 37(2), 1998, pp. 363-375
We characterized a novel giant Gypsy-like retrotransposon, CE,clops, p
resent in about 5000 copies in the genome of Pisum sativum. The indivi
dual element Cyclops-2 measures 12 314 bp including long terminal repe
ats (LTRs) of 1504 bp and 1594 bp, respectively, showing 4.1% sequence
divergence between one another. Cyclops-2 carries a polypurine tract
(PPT) and an unusual primer binding site (PBS) complementary to tRNA-G
lu. The element is bounded by 5 bp target site duplications and harbor
s three successive internal regions with homology to retroviral genes
gag (424 codons) and pol (1382 codons) and an additional open reading
frame (423 codons) of unknown function indicating the element's potent
ial capacity for gene transduction. The pol region contains sequence m
otifs related to the enzymes protease, reverse transcriptase, RNAse H
and integrase in the same typical order (5'-PR-RT-RH-IN-3') known for
retroviruses and Gypsy-like retrotransposons. The reading frame of the
pol region is disrupted by several mutations suggesting that Cyclops-
2 does not encode functional enzymes. A phylogenetic analysis of the r
everse transcriptase domain confirms our differential genetic assessme
nt that Cyclops from pea is a novel element with no specific relations
hip to the previously described Gypsy-like elements from plants. Genom
ic Southern hybridizations show that Cyclops is abundant not only in p
ea but also in common bean, mung bean, broad bean, soybean and the pea
nut suggesting that Cyclops may be an useful genetic tool for analyzi
ng the genomes of agronomically important legumes.