Abstract
Three families of retrotransposons of rice (Tos1, Tos2, and Tos3) were isolated by using a method based on the sequence conservation of the primer binding site for reverse transcription. This method should be generally applicable for cloning retrotransposon of other plants. One retrotransposon, Tos3-1, was studied in detail. Tos3-1 is 5.2 kb long, has structures common to retrotransposons, such as long terminal repeats (LTR), a primer binding site complementary to the initiator tRNA, a polypurine tract, and generates target sequence duplications flanking the inserted element. Southern blotting analysis showed that sequences homologous to Tos1, 2 and 3 are found in wild rice species as well as in cultivated rice species, but not in maize and tobacco. The copy number and genomic location of the families vary in different strains of one species of wild rice, suggesting that these elements may still be active. Retrotransposons were also screened for by amplification of the reverse transcriptase coding region using the polymerase chain reaction (PCR). At least two types of copia-like elements (Tos4 and Tos5) were found. The total copy number of retrotransposons in the rice genome was estimated to be about 1000. These results suggest that, as in Drosophila, retrotransposons are the major transposon class in rice.
MeSH Terms
Amino Acid Sequence
Base Sequence
Cloning, Molecular
DNA
DNA Transposable Elements
Molecular Sequence Data
Nucleic Acid Hybridization
Oryza/genetics
Polymerase Chain Reaction
RNA-Directed DNA Polymerase/genetics
Repetitive Sequences, Nucleic Acid
Restriction Mapping
Chemicals
DNA Transposable Elements
DNA
RNA-Directed DNA Polymerase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hirochika H
Department of Molecular Biology, National Institute of Agrobiological Resources, Ibaraki, Japan.
Fukuchi A
Kikuchi F
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