Characterization of long terminal repeat sequences of HTLV-III

Science ◽  
1985 ◽  
Vol 227 (4686) ◽  
pp. 538-540 ◽  
Author(s):  
B Starcich ◽  
L Ratner ◽  
S. Josephs ◽  
T Okamoto ◽  
R. Gallo ◽  
...  
2020 ◽  
Vol 36 (6) ◽  
pp. 533-538
Author(s):  
Sathiaseelan Manohar Nesakumar ◽  
Haribabu Hemalatha ◽  
KK Vidyavijayan ◽  
Karunakaran Lucia Precilla ◽  
Karunaianantham Ramesh ◽  
...  

2013 ◽  
Vol 29 (5) ◽  
pp. 837-841 ◽  
Author(s):  
Geraldo A. Ferraro ◽  
Joana P. Monteiro-Cunha ◽  
Flora M.C. Fernandes ◽  
Aline C.A. Mota-Miranda ◽  
Carlos Brites ◽  
...  

1987 ◽  
Vol 7 (4) ◽  
pp. 1559-1562
Author(s):  
J Silver ◽  
A Rabson ◽  
T Bryan ◽  
R Willey ◽  
M A Martin

Novel endogenous human retroviral sequences were cloned by low-stringency hybridization, using the pol gene of endogenous human retrovirus 51-1. One clone, lambda NP-2, contained gag, pol, env, and long terminal repeat sequences related to the corresponding portions of clone 51-1 and the closely related full-length endogenous human retrovirus 4-1. The sequence of the env gene of NP-2 was 73% homologous to that of 4-1. Genomic Southern blots of male and female DNAs showed that NP-2 is located on the Y chromosome and that the Y chromosome also contains one other sequence closely related to the env and 3' flanking regions of NP-2. Conservation of flanking DNA suggests that the second Y chromosome copy of the NP-2 env sequence arose by gene duplication rather than provirus insertion.


1987 ◽  
Vol 7 (4) ◽  
pp. 1559-1562 ◽  
Author(s):  
J Silver ◽  
A Rabson ◽  
T Bryan ◽  
R Willey ◽  
M A Martin

Novel endogenous human retroviral sequences were cloned by low-stringency hybridization, using the pol gene of endogenous human retrovirus 51-1. One clone, lambda NP-2, contained gag, pol, env, and long terminal repeat sequences related to the corresponding portions of clone 51-1 and the closely related full-length endogenous human retrovirus 4-1. The sequence of the env gene of NP-2 was 73% homologous to that of 4-1. Genomic Southern blots of male and female DNAs showed that NP-2 is located on the Y chromosome and that the Y chromosome also contains one other sequence closely related to the env and 3' flanking regions of NP-2. Conservation of flanking DNA suggests that the second Y chromosome copy of the NP-2 env sequence arose by gene duplication rather than provirus insertion.


Virus Genes ◽  
2017 ◽  
Vol 53 (3) ◽  
pp. 386-391 ◽  
Author(s):  
Yan-ping Zhang ◽  
Ke-yan Bao ◽  
Guo-rong Sun ◽  
Hong-chao Lv ◽  
Hong-yu Cui ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document