AI Article Synopsis

  • Human Endogenous Retroviruses type K HML-2 (HK2) include newly discovered proviruses, K111 and K222, which are notably found in pericentromeric regions of the human genome.
  • Researchers utilized PCR and sequencing to analyze the K111 provirus across various ethnic groups and disease contexts.
  • The results show that a deletion of the K111 provirus is linked to increased severity in Cutaneous T-cell lymphoma (CTCL) among Caucasians and appears to influence T-cell survival in HIV infection, highlighting its evolutionary significance and origins out of Africa.

Article Abstract

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498702PMC
http://dx.doi.org/10.1186/s12920-019-0505-8DOI Listing

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Article Synopsis
  • Human Endogenous Retroviruses type K HML-2 (HK2) include newly discovered proviruses, K111 and K222, which are notably found in pericentromeric regions of the human genome.
  • Researchers utilized PCR and sequencing to analyze the K111 provirus across various ethnic groups and disease contexts.
  • The results show that a deletion of the K111 provirus is linked to increased severity in Cutaneous T-cell lymphoma (CTCL) among Caucasians and appears to influence T-cell survival in HIV infection, highlighting its evolutionary significance and origins out of Africa.
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Human papillomavirus (HPV) E2 proteins are integral for the transcription of viral genes and the replication and maintenance of viral genomes in host cells. E2 recruits the viral DNA helicase E1 to the origin. A lysine (K111), highly conserved among almost all papillomavirus (PV) E2 proteins, is a target for P300 (EP300) acetylation and is critical for viral DNA replication (E.

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