iBet uBet web content aggregator. Adding the entire web to your favor.
iBet uBet web content aggregator. Adding the entire web to your favor.



Link to original content: https://pubmed.ncbi.nlm.nih.gov/25734056/
Transcriptional activity of human endogenous retroviruses in human peripheral blood mononuclear cells - PubMed Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015:2015:164529.
doi: 10.1155/2015/164529. Epub 2015 Feb 5.

Transcriptional activity of human endogenous retroviruses in human peripheral blood mononuclear cells

Affiliations

Transcriptional activity of human endogenous retroviruses in human peripheral blood mononuclear cells

Emanuela Balestrieri et al. Biomed Res Int. 2015.

Abstract

Human endogenous retroviruses (HERVs) have been implicated in human physiology and in human pathology. A better knowledge of the retroviral transcriptional activity in the general population and during the life span would greatly help the debate on its pathologic potential. The transcriptional activity of four HERV families (H, K, W, and E) was assessed, by qualitative and quantitative PCR, in PBMCs from 261 individuals aged from 1 to 80 years. Our results show that HERV-H, HERV-K, and HERV-W, but not HERV-E, are transcriptionally active in the test population already in the early childhood. In addition, the transcriptional levels of HERV-H, HERV-K, and HERV-W change significantly during the life span, albeit with distinct patterns. Our results, reinforce the hypothesis of a physiological correlation between HERVs activity and the different stages of life in humans. Studies aiming at identifying the factors, which are responsible for these changes during the individual's life, are still needed. Although the observed phenomena are presumably subjected to great variability, the basal transcriptional activity of each individual, also depending on the different ages of life, must be carefully considered in all the studies involving HERVs as causative agents of disease.

PubMed Disclaimer

Figures

Figure 1
Figure 1
HERV-W transcription activity in human PBMCs, by qualitative RT-PCR. An example of agarose gel analysis is shown. Briefly, RNA from human PBMCs was retrotranscribed and amplified by RT-PCR, using degenerated primers to assess the different virus types belonging to HERV-W family; samples in which PCR products could be visualized were defined as positive for HERV-W expression (lanes 2, 3, 4, and 6), while samples in which no specific band could be detected were defined as negative (lanes 1 and 5).
Figure 2
Figure 2
HERV-H, HERV-K, and HERV-W transcriptional levels in human PBMCs. Data are represented as box plot, depicting mild (black dot) and extreme outliers (asterisk). Relative env levels were analyzed by real-time PCR and represented by 2−ΔΔCt in logarithmic scale.
Figure 3
Figure 3
Correlation of HERV-H, HERV-K, or HERV-W env levels with the age of the subjects. HERV-H, HERV-K, and HERV-W transcriptional levels are plotted as a function of corresponding age in years. The age median value of the age-group (18–39) was used as a cut-point (left panel: <30; right panel: ≥30). See Results section for correlation Spearman analysis details. env levels were analyzed by real-time PCR and represented by 2−ΔΔCt in logarithmic scale.

Similar articles

Cited by

References

    1. Lander E. S., Linton L. M., Birren B., et al. Initial sequencing and analysis of the human genome. Nature. 2001;409(6822):860–921. doi: 10.1038/35057062. - DOI - PubMed
    1. Cordaux R., Batzer M. A. The impact of retrotransposons on human genome evolution. Nature Reviews Genetics. 2009;10(10):691–703. doi: 10.1038/nrg2640. - DOI - PMC - PubMed
    1. Deininger P. L., Moran J. V., Batzer M. A., Kazazian H. H., Jr. Mobile elements and mammalian genome evolution. Current Opinion in Genetics & Development. 2003;13(6):651–658. doi: 10.1016/j.gde.2003.10.013. - DOI - PubMed
    1. Ohno S. So much ‘junk’ DNA in our genome. Brookhaven Symposia in Biology. 1972;23:366–370. - PubMed
    1. Carreira P. E., Richardson S. R., Faulkner G. J. L1 retrotransposons, cancer stem cells and oncogenesis. FEBS Journal. 2014;281(1):63–73. doi: 10.1111/febs.12601. - DOI - PMC - PubMed

Publication types