The 441-bp DNA segment in a PCR-amplified fragment from Oryza sativa cv. IR
36 was found to have a sequence with features characteristic of LTRs of ret
roelements, which was named RIRE2 (Rice retroelement #2) and further analyz
ed. Cloning and sequencing analyses of the DNA segments connected to LTR-li
ke sequence showed that RIRE2 has a long internal region almost 10 kb long
that is flanked by LTR-like sequences. This internal region carries a prime
r binding site (PBS) and polypurine tract (PPT) which are necessary for cDN
A synthesis of retroelements. The PBS sequence is complementary to the 3' e
nd region of tRNA(Arg). The internal region has an rt gene homologous to th
at of gypsy-type retrotransposons, evidence that RIRE2 is indeed a retrotra
nsposon related to gypsy from Drosophila. RIRE2 has an extra sequence more
than 4 kb long in the region downstream of gag-pol. Phylogenetic analysis o
f the putative amino-acid sequences of the rt gene as well as the int gene
showed that RIRE2 is related to a group of gypsy-type retrotransposons of a
large size that include Grande1-4 of teosinte, Tat4-1 and Athila1-1 of Ara
bidopsis thaliana, and Cyclops-2 of pea, but distantly related to any other
group of gypsy-type retrotransposons, including RIRE3 and RIRE8 of rice. R
IRE2 and Grande1-4 had the highest homology in the gag-pol region, but the
nucleotide sequences of the LTR regions differed. Both elements had signifi
cant homology in the middle area of the extra regions downstream of gag-pol
, in which they had an open reading frame encoding a protein with no known
function on the opposite strand from that coding for gag-pol.