J Pediatr Genet 2014; 03(01): 009-016
DOI: 10.3233/PGE-14081
Review
Georg Thieme Verlag KG Stuttgart – New York

Retrotransposons and pediatric genetic disorders: Importance and implications

Seyed Mohammad Akrami
a   Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
,
Laleh Habibi
a   Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
b   Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
› Author Affiliations

Subject Editor:
Further Information

Publication History

19 April 2014

25 May 2014

Publication Date:
27 July 2015 (online)

Abstract

Pediatric disorders are generally observed to have a greater genetic load than diseases occurring during adulthood. Clinical manifestations of many genetic defects including chromosomal abnormalities and mutations in specific genes appear during childhood. One of the notable mutagens in human cells is mobile DNA element. They possess the ability to move and insert themselves in new genomic locations including critical disease-causing genes. Although our cells inhibit their transport by different mechanisms, factors such as aging and environmental heavy metals have effect on increasing their activities. In this article, we try to go over the features of active human retroelements and highlight their role in the pathology of pediatric genetic disorders. We also propose two mechanisms in which aged parental gametes and embryonic exposure to environmental stresses followed by mobile elements insertion may result in de novo pediatric diseases.