scholarly journals Faculty Opinions recommendation of The human leukemia virus HTLV-1 alters the structure and transcription of host chromatin in cis.

Author(s):  
Yutaka Tagaya
2018 ◽  
Author(s):  
Anat Melamed ◽  
Hiroko Yaguchi ◽  
Michi Miura ◽  
Aviva Witkover ◽  
Tomas W Fitzgerald ◽  
...  

eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Anat Melamed ◽  
Hiroko Yaguchi ◽  
Michi Miura ◽  
Aviva Witkover ◽  
Tomas W Fitzgerald ◽  
...  

Chromatin looping controls gene expression by regulating promoter-enhancer contacts, the spread of epigenetic modifications, and the segregation of the genome into transcriptionally active and inactive compartments. We studied the impact on the structure and expression of host chromatin by the human retrovirus HTLV-1. We show that HTLV-1 disrupts host chromatin structure by forming loops between the provirus and the host genome; certain loops depend on the critical chromatin architectural protein CTCF, which we recently discovered binds to the HTLV-1 provirus. We show that the provirus causes two distinct patterns of abnormal transcription of the host genome in cis: bidirectional transcription in the host genome immediately flanking the provirus, and clone-specific transcription in cis at non-contiguous loci up to >300 kb from the integration site. We conclude that HTLV-1 causes insertional mutagenesis up to the megabase range in the host genome in >104 persistently-maintained HTLV-1+ T-cell clones in vivo.


2018 ◽  
Author(s):  
Anat Melamed ◽  
Hiroko Yaguchi ◽  
Michi Miura ◽  
Aviva Witkover ◽  
Tomas W Fitzgerald ◽  
...  

AbstractChromatin looping controls gene expression by regulating promoter-enhancer contacts, the spread of epigenetic modifications, and the segregation of the genome into transcriptionally active and inactive compartments. We studied the impact on the structure and expression of host chromatin by the human retrovirus HTLV-1. We show that HTLV-1 disrupts host chromatin structure by forming loops between the provirus and the host genome; certain loops depend on the critical chromatin architectural protein CTCF, which we recently showed binds to the HTLV-1 provirus. Finally, we show that the provirus causes two distinct patterns of abnormal transcription of the host genome in cis: bidirectional transcription in the host genome immediately flanking the provirus, and clone-specific transcription in cis at non-contiguous loci up to >300 kb from the integration site. We conclude that HTLV-1 causes insertional mutagenesis up to the megabase range in the host genome in >104 persistently-maintained HTLV-1+ T-cell clones in vivo.


1993 ◽  
Vol 19 (2) ◽  
pp. 489-503
Author(s):  
K. Nishioka ◽  
T. Nakajima ◽  
T. Hasunuma ◽  
K. Sato

1964 ◽  
Vol 85 (11) ◽  
pp. 173
Author(s):  
Faye Marley

1980 ◽  
Vol 29 (2) ◽  
pp. 311-315
Author(s):  
D R Mayo ◽  
F Rapp

Mice infected with 2 x 10(3) plaque-forming units of mouse cytomegalovirus (MCMV) 3 days after receiving 300 to 400 spleen focus-forming units of Friend leukemia virus developed a more severe MCMV infection than did normal animals. Increased severity was demonstrated by the increased amounts of MCMV recoverable from the salivary glands of leukemic mice 1 to 5 weeks postinfection. In addition, the difference in the number of virus isolations from the kidneys, spleens, livers, and lungs of animals (74 to 120) coinfected with MCMV and Friend leukemia virus compared with animals (49 of 120) infected with MCMV alone was significant (P less than 0.01). Both the 50% lethal dose and 50% infectious dose of MCMV in leukemic mice were lower than in normal animals. MCMV and Friend leukemia virus appear to interact by suppressing the ability of infected spleen cells to respond to mitogen-induced stimulation. The observations of increased severity of MCMV infections in leukemic mice closely parallel the situation observed in human leukemia patients who are at an increased risk of disease due to human cytomegalovirus infections. This mouse model may be useful in assessing the effect of antiviral (cytomegalovirus) therapy.


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