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ISOLATION AND CHARACTERIZATION OF A HIGHLY DIVERGENT HIV-2[GH-2] - GENERATION OF AN INFECTIOUS MOLECULAR CLONE AND FUNCTIONAL-ANALYSIS OF ITS REV-RESPONSIVE ELEMENT IN RESPONSE TO PRIMATE RETROVIRUS TRANSACTIVATORS (REV AND REX)
被引:9
作者:
KAWAMURA, M
KATAHIRA, J
FUKASAWA, M
SAKURAGI, JI
ISHIKAWA, KI
NAKAI, M
MINGLE, JAA
OSEIKWASI, M
NETTY, VBA
AKARI, H
HISHIDA, O
TOMONAGA, K
MIURA, T
HAYAMI, M
机构:
[1] KYOTO UNIV,IMMUNODEFICIENCY VIRUS RES CTR,SAKYO KU,KYOTO 606,JAPAN
[2] INST PUBL HLTH,YAMANASHI,JAPAN
[3] OSAKA MED COLL,TAKATSUKI,OSAKA 569,JAPAN
[4] UNIV GHANA,NOGUCHI MEM INST MED RES,ACCRA,GHANA
[5] ST JOSEPH HOSP,KOFORIDUA,GHANA
来源:
关键词:
D O I:
10.1016/0042-6822(92)90540-6
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
A highly divergent HIV-2 designated as HIV-2[GH-2] was obtained from an AIDS-related complex (ARC) patient in Ghana. A full-length molecular clone of this isolate was obtained and a biologically active clone was constructed. Its restriction pattern differed from that of prototype HIV-2[GH-1 ] in 25 of 35 restriction sites, but was strikingly similarto a previously characterized HIV-2 isolate from a Ghanaian (HIV-2ALT). The conserved integrase region (288-bp fragment) previously displayed 95% identity with that of ALT but 17-20% divergence from the HIV-2 prototype member, and a new distinct subgroup (HIV-2b) of HIV-2 consisting of GH-2 and ALT was postulated (Miura et al. 1991.) These isolates, however, were biologically distinguishable from each other by its replication capacity in a monocyte line, U937, in which GH-2 could not grow but ALT grew well. In addition, the nucleotide sequence of the LTR of this new isolate displays 21% divergence from that of prototype HIV-2[GH-1], but the core enhancer, Spl binding sites and TATA box were conserved. Although the 3' half of the env gene sequence which is deleted in HIV-2ALT clone showed 27% diversity from the prototype, functional differences in the rev-responsive element were not observed. © 1992.
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页码:850 / 853
页数:4
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