The complete sequence of ART-CB, a recently found chicken retrotranspo
son (A. V. Gudkov, E. A. Komarova, M. A. Nikiforov, and T. E. Zaitsevs
kaya, J. Virol. 66:1726-1736, 1992), was characterized. ART-CH has the
structure of a 3,300-bp-long provirus, including two 388-bp long term
inal repeats (LTRs) (U3, 245 bp; R region, 17 bp; and U5, 126 bp), a t
RNA(Trp)-binding site, and a polypurine tract, similar to avian leukos
is viruses. At least some of the approximately 50 genomic copies of AR
T-CH are transcribed into polyadenylated RNA, which is initiated and t
erminated at the expected sites within the LTRs. In contrast to the re
gulatory sequences involved in proviral expression and replication, th
e internal regions of ART-CH seem to be completely defective. Several
short regions of homology with avian leukosis virus genes, most of whi
ch encode gag-related sequences, were found among different reading fr
ames of ART-CH, which are not organized like regular retroviral genes.
Both sequence analysis and restriction fragment length polymorphism a
nalysis revealed a high degree of sequence (97% homology) and structur
al similarity among members of the ART-CII family, indicating their co
mmon origin and recent penetration into chicken DNA. ART-CK sequences
were detected in mouse cells infected with Rous sarcoma virus produced
by an ART-CH-expressing Rous sarcoma. These data are consistent with
the hypothesis that ART-CH belongs to a class of defective retrotransp
osons whose replication strategy requires the use of helper viruses. T
hey might originate from an avian leukosis virus-related retrovirus wh
ich completely lost its coding capacities as a result of multiple muta
tions and deletions. These features apparently group ART-CH with the V
L30 retrotransposons of rhodents.