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J Virol, March 1998, p. 2272-2279, Vol. 72, No. 3
Laboratory of Gene Technology and Safety,
Tsukuba Life Science Center, The Institute of Physical and Chemical
Research (RIKEN), Tsukuba, Ibaraki 305, Japan
Received 18 August 1997/Accepted 3 December 1997
We previously reported (N. Watanabe, M. Nishi, Y. Ikawa, and H. Amanuma, J. Virol. 65:132-137, 1991) that the mutant Friend spleen focus-forming virus (F-SFFVMS), which encodes a
mutant gp55 membrane glycoprotein with an ecotropic env
gp70 sequence, was nonpathogenic. Here we injected the
F-SFFVMS-Friend murine leukemia virus (F-MuLV) clone 57 complex into newborn DBA/2 mice. We obtained four groups of pathogenic
variant F-SFFV complexes, each showing a different degree of
pathogenicity in adult mice and a different gp55 profile. Of these,
group 1 variant F-SFFV was particularly interesting, because it was the
most frequently obtained and because it produced doublet bands of gp55
(59 and 57 kDa), neither of which reacted with the nonecotropic
gp70-specific monoclonal antibody, and because its DNA intermediate did
not hybridize with the nonecotropic env-specific probe.
Cloning and DNA sequence analysis of the env region of one
isolate of the group 1 variant F-SFFV revealed that this virus
consisted of two distinct F-SFFV genomes; one (clone 117) differed from
the other (clone 118) due to the presence of a 39-bp in-frame deletion. Reconstitution to full-length F-SFFV genomes and a pathogenicity assay
showed that each reconstituted F-SFFV was pathogenic, with clone 117 showing a higher degree of pathogenicity than clone 118. Both
reconstituted F-SFFVs caused activation of the mouse erythropoietin
receptor in the factor-independent cell proliferation assay, although
much less efficiently than the wild-type polycythemia-inducing isolate
F-SFFVp. Clone 118 produced a gp55 of 59 kDa, while clone 117 produced
one of 57 kDa. Clone 118 had a substitution by the F-MuLV clone 57 gp70
sequence, indicating that it was derived from the F-SFFVMS
env gene by a homologous recombination with the F-MuLV
clone 57 env gene. The site of the 39-bp deletion in clone
117 corresponded to the portion of the clone 118 sequence which was
unique to the ecotropic env genes. These results indicated the importance for the biological activity of gp55 of the sequences in
the gp70 differential region, which are contained in both polytropic and ecotropic env genes.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Sequence Flexibility in the Polytropic
env gp70-Derived Region of the Membrane Glycoprotein (gp55)
of Friend Spleen Focus-Forming Virus Affects Its Biological
Activity
*
Corresponding author. Mailing address: Laboratory of
Gene Technology and Safety, Tsukuba Life Science Center, The Institute of Physical and Chemical Research (RIKEN), 3-1-1 Koyadai, Tsukuba, Ibaraki 305, Japan. Phone: 81-298-36-9051. Fax: 81-298-36-9050. E-mail:
amanuma{at}rtc.riken.go.jp.
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