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Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection

BACKGROUND: Human Endogenous Retroviruses type K HML-2 (HK2) are integrated into 117 or more areas of human chromosomal arms while two newly discovered HK2 proviruses, K111 and K222, spread extensively in pericentromeric regions, are the first retroviruses discovered in these areas of our genome. ME...

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Autores principales: Kaplan, Mark H., Kaminski, Mark, Estes, Judith M., Gitlin, Scott D., Zahn, Joseph, Elder, James T., Tejasvi, Trilokraj, Gensterblum, Elizabeth, Sawalha, Amr H., McGowan, Joseph Patrick, Dosik, Michael H., Direskeneli, Haner, Direskeneli, Guher Saruhan, Adebamowo, Sally N., Adebamowo, Clement A., Sajadi, Mohammad, Contreras-Galindo, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498702/
https://www.ncbi.nlm.nih.gov/pubmed/31046767
http://dx.doi.org/10.1186/s12920-019-0505-8
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author Kaplan, Mark H.
Kaminski, Mark
Estes, Judith M.
Gitlin, Scott D.
Zahn, Joseph
Elder, James T.
Tejasvi, Trilokraj
Gensterblum, Elizabeth
Sawalha, Amr H.
McGowan, Joseph Patrick
Dosik, Michael H.
Direskeneli, Haner
Direskeneli, Guher Saruhan
Adebamowo, Sally N.
Adebamowo, Clement A.
Sajadi, Mohammad
Contreras-Galindo, Rafael
author_facet Kaplan, Mark H.
Kaminski, Mark
Estes, Judith M.
Gitlin, Scott D.
Zahn, Joseph
Elder, James T.
Tejasvi, Trilokraj
Gensterblum, Elizabeth
Sawalha, Amr H.
McGowan, Joseph Patrick
Dosik, Michael H.
Direskeneli, Haner
Direskeneli, Guher Saruhan
Adebamowo, Sally N.
Adebamowo, Clement A.
Sajadi, Mohammad
Contreras-Galindo, Rafael
author_sort Kaplan, Mark H.
collection PubMed
description BACKGROUND: Human Endogenous Retroviruses type K HML-2 (HK2) are integrated into 117 or more areas of human chromosomal arms while two newly discovered HK2 proviruses, K111 and K222, spread extensively in pericentromeric regions, are the first retroviruses discovered in these areas of our genome. METHODS: We use PCR and sequencing analysis to characterize pericentromeric K111 proviruses in DNA from individuals of diverse ethnicities and patients with different diseases. RESULTS: We found that the 5′ LTR-gag region of K111 proviruses is missing in certain individuals, creating pericentromeric instability. K111 deletion (−/− K111) is seen in about 15% of Caucasian, Asian, and Middle Eastern populations; it is missing in 2.36% of African individuals, suggesting that the −/− K111 genotype originated out of Africa. As we identified the −/−K111 genotype in Cutaneous T-cell lymphoma (CTCL) cell lines, we studied whether the −/−K111 genotype is associated with CTCL. We found a significant increase in the frequency of detection of the −/−K111 genotype in Caucasian patients with severe CTCL and/or Sézary syndrome (n = 35, 37.14%), compared to healthy controls (n = 160, 15.6%) [p = 0.011]. The −/−K111 genotype was also found to vary in HIV-1 infection. Although Caucasian healthy individuals have a similar frequency of detection of the −/− K111 genotype, Caucasian HIV Long-Term Non-Progressors (LTNPs) and/or elite controllers, have significantly higher detection of the −/−K111 genotype (30.55%; n = 36) than patients who rapidly progress to AIDS (8.5%; n = 47) [p = 0.0097]. CONCLUSION: Our data indicate that pericentromeric instability is associated with more severe CTCL and/or Sézary syndrome in Caucasians, and appears to allow T-cells to survive lysis by HIV infection. These findings also provide new understanding of human evolution, as the −/−K111 genotype appears to have arisen out of Africa and is distributed unevenly throughout the world, possibly affecting the severity of HIV in different geographic areas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12920-019-0505-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-64987022019-05-09 Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection Kaplan, Mark H. Kaminski, Mark Estes, Judith M. Gitlin, Scott D. Zahn, Joseph Elder, James T. Tejasvi, Trilokraj Gensterblum, Elizabeth Sawalha, Amr H. McGowan, Joseph Patrick Dosik, Michael H. Direskeneli, Haner Direskeneli, Guher Saruhan Adebamowo, Sally N. Adebamowo, Clement A. Sajadi, Mohammad Contreras-Galindo, Rafael BMC Med Genomics Research Article BACKGROUND: Human Endogenous Retroviruses type K HML-2 (HK2) are integrated into 117 or more areas of human chromosomal arms while two newly discovered HK2 proviruses, K111 and K222, spread extensively in pericentromeric regions, are the first retroviruses discovered in these areas of our genome. METHODS: We use PCR and sequencing analysis to characterize pericentromeric K111 proviruses in DNA from individuals of diverse ethnicities and patients with different diseases. RESULTS: We found that the 5′ LTR-gag region of K111 proviruses is missing in certain individuals, creating pericentromeric instability. K111 deletion (−/− K111) is seen in about 15% of Caucasian, Asian, and Middle Eastern populations; it is missing in 2.36% of African individuals, suggesting that the −/− K111 genotype originated out of Africa. As we identified the −/−K111 genotype in Cutaneous T-cell lymphoma (CTCL) cell lines, we studied whether the −/−K111 genotype is associated with CTCL. We found a significant increase in the frequency of detection of the −/−K111 genotype in Caucasian patients with severe CTCL and/or Sézary syndrome (n = 35, 37.14%), compared to healthy controls (n = 160, 15.6%) [p = 0.011]. The −/−K111 genotype was also found to vary in HIV-1 infection. Although Caucasian healthy individuals have a similar frequency of detection of the −/− K111 genotype, Caucasian HIV Long-Term Non-Progressors (LTNPs) and/or elite controllers, have significantly higher detection of the −/−K111 genotype (30.55%; n = 36) than patients who rapidly progress to AIDS (8.5%; n = 47) [p = 0.0097]. CONCLUSION: Our data indicate that pericentromeric instability is associated with more severe CTCL and/or Sézary syndrome in Caucasians, and appears to allow T-cells to survive lysis by HIV infection. These findings also provide new understanding of human evolution, as the −/−K111 genotype appears to have arisen out of Africa and is distributed unevenly throughout the world, possibly affecting the severity of HIV in different geographic areas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12920-019-0505-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-02 /pmc/articles/PMC6498702/ /pubmed/31046767 http://dx.doi.org/10.1186/s12920-019-0505-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kaplan, Mark H.
Kaminski, Mark
Estes, Judith M.
Gitlin, Scott D.
Zahn, Joseph
Elder, James T.
Tejasvi, Trilokraj
Gensterblum, Elizabeth
Sawalha, Amr H.
McGowan, Joseph Patrick
Dosik, Michael H.
Direskeneli, Haner
Direskeneli, Guher Saruhan
Adebamowo, Sally N.
Adebamowo, Clement A.
Sajadi, Mohammad
Contreras-Galindo, Rafael
Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection
title Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection
title_full Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection
title_fullStr Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection
title_full_unstemmed Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection
title_short Structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous T-cell lymphoma, Sézary syndrome, and HIV infection
title_sort structural variation of centromeric endogenous retroviruses in human populations and their impact on cutaneous t-cell lymphoma, sézary syndrome, and hiv infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498702/
https://www.ncbi.nlm.nih.gov/pubmed/31046767
http://dx.doi.org/10.1186/s12920-019-0505-8
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