Last year we reported the molecular cloning of D4/CYN/CA and D5/HRE/OR. We now describe the deduced amino acid sequence encoded by the complete D5/RHE/OR genome, and the sequence of the D4/CYN/CA env glycoprotein. The D5/RHE/OR genome contains the prototypical type D genetic structure (5'LTR-gag-prt-pol-env-3'LTR) and encodes a truncated 8045 bp provirus. The 5' LTR is 329 bp in length and possesses typical retroviral determinants of integration, replication and expression, including the U3, R and U5 regions, candidate TATA box and CAT sequences, and the potential polyadenylation signal. Interestingly, unlike all other molecularly-cloned SRVs, the D5/RHE/OR polyadenylation signal is identical to the signal found in most eukaryotic genes and in other viruses. The D5/RHE/OR gag gene encodes a polyprotein of 660 amino acids. As in all SRVs, the gag polyprotein contains the processed gag molecules p10, pp24/pp18, p12, p27, p14 and p4. The D5/RHE/OR viral protease is 314 amino acids long and contains a common Asp-Thr-Gly motif; the prt gene overlaps the gag gene by 61 residues, and the pol gene by 8 residues. The D5/RHE/OR pol gene encodes a product of 864 amino acids, which is 3 residues shorter than the pol products of other SRVs. The D5/RHE/OR env polyprotein is 585 amino acid residues long (gp70 and gp20 molecules are 394 and 191 amino acid residues, respectively), and contains 12 Asn-X-Ser(Thr) glycosylation sites, 11 of which are found within gp70. The D4/CYN/CA envelope polyprotein is 582 amino acids long (gp70 and gp20 molecules are 390 and 192 residues, respectively). The D4/CYN/CA gp70 and gp20 molecules are 61.8-68.7% (range) and 84.9-87.5% (range), similar to corresponding env glycoproteins identified for all other SRV serogroups. The comparison of D4/CYN/CA and D5/RHE/OR sequences to all other molecularly-cloned SRVs has provided valuable insight concerning the evolutionary divergence of the type D simian retrovirus family.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000163-39
Application #
6277347
Study Section
Project Start
1998-05-01
Project End
1999-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
39
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Oregon Regional Primate Research Center
Department
Type
DUNS #
City
Beaverton
State
OR
Country
United States
Zip Code
97006
Okoye, Afam A; Hansen, Scott G; Vaidya, Mukta et al. (2018) Early antiretroviral therapy limits SIV reservoir establishment to delay or prevent post-treatment viral rebound. Nat Med 24:1430-1440
Jensen, Jeffrey T; Hanna, Carol; Mishler, Emily et al. (2018) Effect of menstrual cycle phase and hormonal treatments on evaluation of tubal patency in baboons. J Med Primatol 47:40-45
Toro, C A; Aylwin, C F; Lomniczi, A (2018) Hypothalamic epigenetics driving female puberty. J Neuroendocrinol 30:e12589
Bulgarelli, Daiane L; Ting, Alison Y; Gordon, Brenda J et al. (2018) Development of macaque secondary follicles exposed to neutral red prior to 3-dimensional culture. J Assist Reprod Genet 35:71-79
Prola-Netto, Joao; Woods, Mark; Roberts, Victoria H J et al. (2018) Gadolinium Chelate Safety in Pregnancy: Barely Detectable Gadolinium Levels in the Juvenile Nonhuman Primate after in Utero Exposure. Radiology 286:122-128
Moccetti, Federico; Brown, Eran; Xie, Aris et al. (2018) Myocardial Infarction Produces Sustained Proinflammatory Endothelial Activation in Remote Arteries. J Am Coll Cardiol 72:1015-1026
Blue, Steven W; Winchell, Andrea J; Kaucher, Amy V et al. (2018) Simultaneous quantitation of multiple contraceptive hormones in human serum by LC-MS/MS. Contraception 97:363-369
Jeon, Sookyoung; Li, Qiyao; Rubakhin, Stanislav S et al. (2018) 13C-lutein is differentially distributed in tissues of an adult female rhesus macaque following a single oral administration: a pilot study. Nutr Res :
Slayden, Ov Daniel; Friason, Francis Kathryn E; Bond, Kise Rosen et al. (2018) Hormonal regulation of oviductal glycoprotein 1 (OVGP1; MUC9) in the rhesus macaque cervix. J Med Primatol 47:362-370
Dissen, G A; Adachi, K; Lomniczi, A et al. (2017) Engineering a gene silencing viral construct that targets the cat hypothalamus to induce permanent sterility: An update. Reprod Domest Anim 52 Suppl 2:354-358

Showing the most recent 10 out of 492 publications