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.

Highlights

  • Retroelements are a major contributor to genome size, constituting approximately 45% of the human genomic DNA [1, 2]

  • Our results show that Human endogenous retroviruses (HERVs)-H, HERV-K, and HERV-W, but not HERV-E, are transcriptionally active in the test population already in the early childhood

  • The major subset of long terminal repeats (LTRs) retrotransposons is represented by the Human Endogenous Retroviruses (HERVs), which constitute about 8% of the human genome [1]

Read more

Summary

Introduction

Retroelements are a major contributor to genome size, constituting approximately 45% of the human genomic DNA [1, 2] They are subdivided, according to size and functionally related structures, into short interspersed elements (SINEs), long interspersed elements (LINEs), long terminal repeat(LTR) retrotransposons, and DNA transposons [3]. In the past these sequences were wrongly defined “junk DNA” because they were thought not to possess any physiological role [4] but always more evidences show that they are subject to natural selection and contribute to the benefits of the host, as well as other genes which make up the genome.

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call